| 1 | The selfish environment meets the selfish gene: Coevolution and inheritance of RNA and DNA pools | 1.7 | 3 | Citations (PDF) |
| 2 | Rapid auditory processing and medial geniculate nucleus anomalies in Kiaa0319 knockout mice | 1.3 | 2 | Citations (PDF) |
| 3 | Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people | 5.3 | 117 | Citations (PDF) |
| 4 | Discovery of 42 genome-wide significant loci associated with dyslexia | 14.2 | 130 | Citations (PDF) |
| 5 | People also looked at | 1.9 | 6 | Citations (PDF) |
| 6 | Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia | 5.6 | 108 | Citations (PDF) |
| 7 | Leslie Brent: Extraordinary Scientist and Truly Remarkable Human Being | 1.7 | 0 | Citations (PDF) |
| 8 | An epigenetic, transgenerational model of increased mental health disorders in children, adolescents and young adults | 2.1 | 42 | Citations (PDF) |
| 9 | Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia | 3.9 | 105 | Citations (PDF) |
| 10 | Infection and Malignancy Outweigh Cardiovascular Mortality in Kidney Transplant Recipients: Post Hoc Analysis of the FAVORIT Trial | 1.6 | 43 | Citations (PDF) |
| 11 | The neuronal migration hypothesis of dyslexia: A critical evaluation 30 years on | 1.7 | 57 | Citations (PDF) |
| 12 | AU040320 deficiency leads to disruption of acrosome biogenesis and infertility in homozygous mutant mice | 2.7 | 20 | Citations (PDF) |
| 13 | Knockout Mice for Dyslexia Susceptibility Gene Homologs KIAA0319 and KIAA0319L have Unaffected Neuronal Migration but Display Abnormal Auditory Processing. | 1.9 | 22 | Citations (PDF) |
| 14 | The Dyslexia-susceptibility Protein KIAA0319 Inhibits Axon Growth Through Smad2 Signaling | 1.9 | 39 | Citations (PDF) |
| 15 | The DCDC2 deletion is not a risk factor for dyslexia | 3.9 | 23 | Citations (PDF) |
| 16 | Does calcium channel blockade have a role in prevention of expression of sepsis in renal transplant recipients? | 1.7 | 5 | Citations (PDF) |
| 17 | The handedness-associated PCSK6 locus spans an intronic promoter regulating novel transcripts. | 2.1 | 11 | Citations (PDF) |
| 18 | Further evidence for a parent-of-origin effect at the NOP9 locus on language-related phenotypes | 1.7 | 60 | Citations (PDF) |
| 19 | Normal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice | 1.6 | 19 | Citations (PDF) |
| 20 | Identification of VPS13C as a Galectin-12-Binding Protein That Regulates Galectin-12 Protein Stability and Adipogenesis | 1.5 | 39 | Citations (PDF) |
| 21 | Reading and Language Disorders: The Importance of Both Quantity and Quality | 1.8 | 45 | Citations (PDF) |
| 22 | Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments | 2.2 | 621 | Citations (PDF) |
| 23 | Genome-wide screening for DNA variants associated with reading and language traits | 1.3 | 124 | Citations (PDF) |
| 24 | Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment | 1.3 | 79 | Citations (PDF) |
| 25 | Associations of HLA alleles with specific language impairment | 1.7 | 73 | Citations (PDF) |
| 26 | A Deletion Involving CD38 and BST1 Results in a Fusion Transcript in a Patient With Autism and Asthma | 1.9 | 35 | Citations (PDF) |
| 27 | Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders | 4.5 | 927 | Citations (PDF) |
| 28 | Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs | 14.2 | 2,307 | Citations (PDF) |
| 29 | Common Variants in Left/Right Asymmetry Genes and Pathways Are Associated with Relative Hand Skill | 2.2 | 145 | Citations (PDF) |
| 30 | Trafficking of the Menkes copper transporter ATP7A is regulated by clathrin-, AP-2–, AP-1–, and Rab22-dependent steps | 1.8 | 66 | Citations (PDF) |
| 31 | Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort | 2.1 | 62 | Citations (PDF) |
| 32 | Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders | 2.2 | 395 | Citations (PDF) |
| 33 | Individual common variants exert weak effects on the risk for autism spectrum disorders. | 2.1 | 360 | Citations (PDF) |
| 34 | CNVs leading to fusion transcripts in individuals with autism spectrum disorder | 2.1 | 36 | Citations (PDF) |
| 35 | Donor Disease Transmission | 1.7 | 0 | Citations (PDF) |
| 36 | Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder | 2.1 | 70 | Citations (PDF) |
| 37 | The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure | 1.5 | 42 | Citations (PDF) |
| 38 | Everolimus and Long-Term Outcomes in Renal Transplantation: Seeking an Optimal Strategy for Immunosuppression | 1.7 | 1 | Citations (PDF) |
| 39 | Chronic Renal Allograft Damage: Not Enough Immunosuppression? | 1.7 | 0 | Citations (PDF) |
| 40 | Chorea-Acanthocytosis Genotype in the Original Critchley Kentucky Neuroacanthocytosis Kindred | 6.9 | 12 | Citations (PDF) |
| 41 | Analysis of dyslexia candidate genes in the Raine cohort representing the general Australian population | 1.3 | 49 | Citations (PDF) |
| 42 | Genome-wide analysis of genetic susceptibility to language impairment in an isolated Chilean population | 2.1 | 53 | Citations (PDF) |
| 43 | Novel method for combined linkage and genome-wide association analysis finds evidence of distinct genetic architecture for two subtypes of autism | 1.7 | 22 | Citations (PDF) |
| 44 | A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3 | 1.7 | 41 | Citations (PDF) |
| 45 | Links between genetics and pathophysiology in the autism spectrum disorders | 4.7 | 41 | Citations (PDF) |
| 46 | PCSK6 is associated with handedness in individuals with dyslexia. | 2.1 | 127 | Citations (PDF) |
| 47 | Rare familial 16q21 microdeletions under a linkage peak implicate cadherin 8 (CDH8) in susceptibility to autism and learning disability | 2.2 | 101 | Citations (PDF) |
| 48 | A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder | 1.9 | 200 | Citations (PDF) |
| 49 | Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits† | 1.0 | 137 | Citations (PDF) |
| 50 | Polymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestry | 2.7 | 59 | Citations (PDF) |
| 51 | A locus for an auditory processing deficit and language impairment in an extended pedigree maps to 12p13.31-q14.3 | 1.3 | 23 | Citations (PDF) |
| 52 | Linkage and candidate gene studies of autism spectrum disorders in European populations | 2.1 | 84 | Citations (PDF) |
| 53 | Functional impact of global rare copy number variation in autism spectrum disorders | 31.8 | 1,941 | Citations (PDF) |
| 54 | Identification of Candidate Genes for Dyslexia Susceptibility on Chromosome 18 | 1.5 | 38 | Citations (PDF) |
| 55 | An allele-specific gene expression assay to test the functional basis of genetic associations. | 0.2 | 2 | Citations (PDF) |
| 56 | A genome-wide scan for common alleles affecting risk for autism. | 2.1 | 576 | Citations (PDF) |
| 57 | The Dyslexia-associated KIAA0319 Protein Undergoes Proteolytic Processing with γ-Secretase-independent Intramembrane Cleavage* | 1.3 | 36 | Citations (PDF) |
| 58 | Disruption at the PTCHD1 Locus on Xp22.11 in Autism Spectrum Disorder and Intellectual Disability | 8.7 | 193 | Citations (PDF) |
| 59 | Gene expression profiling of the donor kidney at the time of transplantation predicts clinical outcomes 2 years after transplantation | 0.5 | 25 | Citations (PDF) |
| 60 | Genetic Advances in the Study of Speech and Language Disorders | 8.7 | 189 | Citations (PDF) |
| 61 | Recent advances in the genetics of language impairment | 5.9 | 128 | Citations (PDF) |
| 62 | Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects | 1.1 | 210 | Citations (PDF) |
| 63 | An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations | 0.2 | 1 | Citations (PDF) |
| 64 | The dyslexia-associated protein KIAA0319 interacts with adaptor protein 2 and follows the classical clathrin-mediated endocytosis pathway | 2.9 | 35 | Citations (PDF) |
| 65 | A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene | 2.2 | 96 | Citations (PDF) |
| 66 | Mapping of partially overlapping de novo deletions across an autism susceptibility region (AUTS5) in two unrelated individuals affected by developmental delays with communication impairment† | 1.1 | 22 | Citations (PDF) |
| 67 | Copy number variation and association analysis of SHANK3 as a candidate gene for autism in the IMGSAC collection | 2.1 | 79 | Citations (PDF) |
| 68 | High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility | 5.6 | 136 | Citations (PDF) |
| 69 | Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment | 1.3 | 93 | Citations (PDF) |
| 70 | Oxidised LDL internalisation by the LOX-1 scavenger receptor is dependent on a novel cytoplasmic motif and is regulated by dynamin-2 | 1.8 | 65 | Citations (PDF) |
| 71 | The dyslexia-associated gene KIAA0319 encodes highly N- and O-glycosylated plasma membrane and secreted isoforms. | 2.1 | 58 | Citations (PDF) |
| 72 | Association of the KIAA0319 Dyslexia Susceptibility Gene With Reading Skills in the General Population | 5.1 | 125 | Citations (PDF) |
| 73 | A Functional Genetic Link between Distinct Developmental Language Disorders | 24.4 | 670 | Citations (PDF) |
| 74 | MET and autism susceptibility: family and case–control studies | 2.1 | 89 | Citations (PDF) |
| 75 | The Genetic Lexicon of Dyslexia | 4.1 | 142 | Citations (PDF) |
| 76 | Activation of ADP-ribosylation factor regulates biogenesis of the ATP7A-containing trans-Golgi network compartment and its Cu-induced trafficking | 2.9 | 26 | Citations (PDF) |
| 77 | Choreoacanthocytosis in a Mexican Family | 6.9 | 11 | Citations (PDF) |
| 78 | Mapping autism risk loci using genetic linkage and chromosomal rearrangements | 14.2 | 1,336 | Citations (PDF) |
| 79 | LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia | 5.6 | 315 | Citations (PDF) |
| 80 | Is ASMT a susceptibility gene for autism spectrum disorders? A replication study in European populations | 5.6 | 49 | Citations (PDF) |
| 81 | Multivariate Linkage Analysis of Specific Language Impairment (SLI) | 1.0 | 51 | Citations (PDF) |
| 82 | Alternative splicing in the dyslexia-associated gene KIAA0319 | 1.3 | 30 | Citations (PDF) |
| 83 | Cell Biology of Membrane Trafficking in Human Disease | 5.5 | 51 | Citations (PDF) |
| 84 | The Fifth Beaune Symposium: Focus on the Vascular Endothelium in Organ Transplantation | 1.7 | 0 | Citations (PDF) |
| 85 | Introduction of Sir Peter John Morris | 1.7 | 0 | Citations (PDF) |
| 86 | Transplantation: A Report of Progress | 1.7 | 0 | Citations (PDF) |
| 87 | Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia | 5.6 | 148 | Citations (PDF) |
| 88 | Determination of the mutation spectrum of the EXT1/EXT2 genes in British Caucasian patients with multiple osteochondromas, and exclusion of six candidate genes in EXT negative cases†‡ | 1.0 | 47 | Citations (PDF) |
| 89 | The chromosome 6p22 haplotype associated with dyslexia reduces the expression of KIAA0319, a novel gene involved in neuronal migration. | 2.1 | 252 | Citations (PDF) |
| 90 | B Cells and Alloantibodies in Tolerance: A New Look | 1.7 | 0 | Citations (PDF) |
| 91 | Care of the Live Kidney Donor | 1.7 | 7 | Citations (PDF) |
| 92 | Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci | 3.2 | 89 | Citations (PDF) |
| 93 | Familial Temporal Lobe Epilepsy as a Presenting Feature of Choreoacanthocytosis | 3.1 | 68 | Citations (PDF) |
| 94 | Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis | 0.9 | 40 | Citations (PDF) |
| 95 | Early Clinical Heterogeneity in Choreoacanthocytosis | 6.9 | 63 | Citations (PDF) |
| 96 | Analysis of IMGSAC autism susceptibility loci: evidence for sex limited and parent of origin specific effects | 2.2 | 120 | Citations (PDF) |
| 97 | Candidate-Gene Screening and Association Analysis at the Autism-Susceptibility Locus on Chromosome 16p: Evidence of Association at GRIN2A and ABAT | 4.5 | 177 | Citations (PDF) |
| 98 | Genetic influences on language impairment and phonological short-term memory | 6.9 | 112 | Citations (PDF) |
| 99 | Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13 | 5.6 | 56 | Citations (PDF) |
| 100 | Severity of disease and risk of malignant change in hereditary multiple exostoses | 2.7 | 199 | Citations (PDF) |
| 101 | Chorein detection for the diagnosis of chorea-acanthocytosis | 4.7 | 202 | Citations (PDF) |
| 102 | Actin and microtubule regulation of Trans-Golgi network architecture, and copper-dependent protein transport to the cell surface | 2.9 | 23 | Citations (PDF) |
| 103 | Analysis of the human gene family | 2.0 | 219 | Citations (PDF) |
| 104 | A 77-Kilobase Region of Chromosome 6p22.2 Is Associated with Dyslexia in Families From the United Kingdom and From the United States | 4.5 | 225 | Citations (PDF) |
| 105 | A meta-analysis from the Cochrane Library reviewing interleukin 2 receptor antagonists in renal transplantation | 1.7 | 0 | Citations (PDF) |
| 106 | Facial transplantation: is the time right? | 1.7 | 7 | Citations (PDF) |
| 107 | Mutation screening and association analysis of six candidate genes for autism on chromosome 7q | 2.1 | 79 | Citations (PDF) |
| 108 | Aberrant trafficking of transmembrane proteins in human disease | 14.4 | 40 | Citations (PDF) |
| 109 | Analysis of reelin as a candidate gene for autism | 5.6 | 121 | Citations (PDF) |
| 110 | Screening of nine candidate genes for autism on chromosome 2q reveals rare nonsynonymous variants in the cAMP-GEFII gene | 5.6 | 113 | Citations (PDF) |
| 111 | A Genomewide Scan for Attention-Deficit/Hyperactivity Disorder in an Extended Sample: Suggestive Linkage on 17p11 | 4.5 | 210 | Citations (PDF) |
| 112 | Confirmatory Evidence for Linkage of Relative Hand Skill to 2p12-q11 | 4.5 | 84 | Citations (PDF) |
| 113 | Use of Multivariate Linkage Analysis for Dissection of a Complex Cognitive Trait | 4.5 | 119 | Citations (PDF) |
| 114 | Genomic studies of gene expression: regulation of the Wilson disease gene | 2.0 | 9 | Citations (PDF) |
| 115 | DECIPHERING THE GENETIC BASIS OF SPEECH AND LANGUAGE DISORDERS | 7.2 | 143 | Citations (PDF) |
| 116 | The Menkes disease ATPase (ATP7A) is internalized via a Rac1-regulated, clathrin- and caveolae-independent pathway. | 2.1 | 41 | Citations (PDF) |
| 117 | Myotubularin-related 2 protein phosphatase and neurofilament light chain protein, both mutated in CMT neuropathies, interact in peripheral nerve. | 2.1 | 68 | Citations (PDF) |
| 118 | FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorderBrain, 2003, 126, 2455-2462 | 6.0 | 352 | Citations (PDF) |
| 119 | Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11. | 2.1 | 62 | Citations (PDF) |
| 120 | Familial and Genetic Effects on Motor Coordination, Laterality, and Reading-Related Cognition | 5.1 | 55 | Citations (PDF) |
| 121 | Tolerance comes of age. Editorial comment | 1.7 | 2 | Citations (PDF) |
| 122 | Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects | 5.6 | 75 | Citations (PDF) |
| 123 | Mutation screening and imprinting analysis of four candidate genes for autism in the 7q32 region | 5.6 | 39 | Citations (PDF) |
| 124 | Novel membrane traffic steps regulate the exocytosis of the Menkes disease ATPase. | 2.1 | 50 | Citations (PDF) |
| 125 | Molecular genetics of speech and language disorders | 1.4 | 15 | Citations (PDF) |
| 126 | Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1 | 0.6 | 64 | Citations (PDF) |
| 127 | A Genomewide Scan for Loci Involved in Attention-Deficit/Hyperactivity Disorder | 4.5 | 308 | Citations (PDF) |
| 128 | Molecular characterization and expression analysis of , mouse homologue of , the Myotubularin-related 2 gene, mutated in CMT4B | 1.6 | 28 | Citations (PDF) |
| 129 | The genetic basis of dyslexia | 24.0 | 78 | Citations (PDF) |
| 130 | Clinical features and molecular bases of neuroacanthocytosis | 2.8 | 191 | Citations (PDF) |
| 131 | Enteric drainage of a pancreas allograft is safe for patients with celiac sprue | 1.0 | 2 | Citations (PDF) |
| 132 | Hailey-Hailey Disease: Molecular and Clinical Characterization of Novel Mutations in the ATP2C1 Gene | 1.8 | 86 | Citations (PDF) |
| 133 | Mutational spectrum of the CHAC gene in patients with chorea-acanthocytosis | 2.1 | 185 | Citations (PDF) |
| 134 | Molecular evolution of FOXP2, a gene involved in speech and language | 31.8 | 1,597 | Citations (PDF) |
| 135 | Autism | 2.2 | 39 | Citations (PDF) |
| 136 | Generating Subclones from Large-Insert Genomic Clones | 1.4 | 0 | Citations (PDF) |
| 137 | Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathy | 0.9 | 34 | Citations (PDF) |
| 138 | The chorea of McLeod syndrome† | 3.2 | 52 | Citations (PDF) |
| 139 | McLeod neuroacanthocytosis: Genotype and phenotype† | 4.7 | 261 | Citations (PDF) |
| 140 | Investigation of Quantitative Measures Related to Reading Disability in a Large Sample of Sib-Pairs from the UK | 1.1 | 37 | Citations (PDF) |
| 141 | A conserved sorting-associated protein is mutant in chorea-acanthocytosis | 14.2 | 392 | Citations (PDF) |
| 142 | A forkhead-domain gene is mutated in a severe speech and language disorder | 31.8 | 2,129 | Citations (PDF) |
| 143 | Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia | 14.2 | 242 | Citations (PDF) |
| 144 | SUPPRESSOR CELLS ARE PRESENT DURING INDUCTION IN MICE MADE TOLERANT WITH ANTILYMPHOCYTE SERUM, DONOR BONE MARROW AND SIROLIMUS. | 1.7 | 1 | Citations (PDF) |
| 145 | EXERCISE TOLERANCE IS SIGNIFICANTLY REDUCED IN RENAL TRANSPLANT RECIPIENTS. | 1.7 | 0 | Citations (PDF) |
| 146 | SAFETY AND ECONOMIC ADVANTAGE OF ROUTINE KETOCONAZOLE USE IN LIVE DONOR RENAL TRANSPLANTATION. | 1.7 | 0 | Citations (PDF) |
| 147 | EXPRESSION OF MHC CLASS II ANTIGEN BY DONOR BONE MARROW CELLS IS ESSENTIAL FOR TOLERANCE INDUCTION IN ALLOGENEIC RADIATION CHIMERA. | 1.7 | 1 | Citations (PDF) |
| 148 | McLeod syndrome and neuroacanthocytosis with a novel mutation in the XK gene | 3.2 | 35 | Citations (PDF) |
| 149 | Charcot-Marie-Tooth type 4B is caused by mutations in the gene encoding myotubularin-related protein-2 | 14.2 | 483 | Citations (PDF) |
| 150 | Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses | 2.1 | 85 | Citations (PDF) |
| 151 | Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca(2+) pump. | 2.1 | 297 | Citations (PDF) |
| 152 | Genetic Refinement and Physical Mapping of the Gene on Chromosome 11q22 | 2.0 | 18 | Citations (PDF) |
| 153 | Characterization of a Highly Complex Region in Xq13 and Mapping of Three Isodicentric Breakpoints Associated with Preleukemia | 2.0 | 14 | Citations (PDF) |
| 154 | A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability | 1.5 | 4 | Citations (PDF) |
| 155 | The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language Disorder | 4.5 | 220 | Citations (PDF) |
| 156 | Identifying Autism Susceptibility Genes | 8.7 | 75 | Citations (PDF) |
| 157 | Autism: recent molecular genetic advances. | 2.1 | 138 | Citations (PDF) |
| 158 | Characterization of the Menkes protein copper-binding domains and their role in copper-induced protein relocalization. | 2.1 | 76 | Citations (PDF) |
| 159 | Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease | 14.2 | 766 | Citations (PDF) |
| 160 | A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia) | 1.7 | 18 | Citations (PDF) |
| 161 | Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostoses | 1.3 | 19 | Citations (PDF) |
| 162 | Electronic identification and chromosomal assignment by radiation hybrid mapping of human expressed sequence tags corresponding to new potassium channel genes | 0.9 | 1 | Citations (PDF) |
| 163 | Serotonin transporter (5-HTT) and γ-aminobutyric acid receptor subunit β3 (GABRB3) gene polymorphisms are not associated with autism in the IMGSA families | 1.1 | 142 | Citations (PDF) |
| 164 | A Quantitative-Trait Locus on Chromosome 6p Influences Different Aspects of Developmental Dyslexia | 4.5 | 263 | Citations (PDF) |
| 165 | A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families. | 2.1 | 302 | Citations (PDF) |
| 166 | Genomic Organization of the Human Gα14 and Gαq Genes and Mutation Analysis in Chorea–Acanthocytosis (CHAC) | 2.0 | 26 | Citations (PDF) |
| 167 | Refined Linkage Disequilibrium and Physical Mapping of the Gene Locus for X-Linked Dystonia–Parkinsonism (DYT3) | 2.0 | 66 | Citations (PDF) |
| 168 | Identification of a di-leucine motif within the C terminus domain of the Menkes disease protein that mediates endocytosis from the plasma membrane | 1.8 | 78 | Citations (PDF) |
| 169 | Molecular Genetic Investigations of Autism | 0.9 | 16 | Citations (PDF) |
| 170 | Integrated physical and transcript map of 5q31.3-qter | 2.1 | 11 | Citations (PDF) |
| 171 | Localisation of a gene implicated in a severe speech and language disorder | 14.2 | 472 | Citations (PDF) |
| 172 | Association of infantile convulsions with paroxysmal dyskinesias (ICCA syndrome): confirmation of linkage to human chromosome 16p12-q12 in a Chinese family | 1.9 | 105 | Citations (PDF) |
| 173 | Recent progress in the genetics of human epilepsies | 0.9 | 16 | Citations (PDF) |
| 174 | Refined Genetic Mapping of the Darier Locus to a <1-cM Region of Chromosome 12q24.1, and Construction of a Complete, High-Resolution P1 Artificial Chromosome/Bacterial Artificial Chromosome Contig of the Critical Region | 4.5 | 22 | Citations (PDF) |
| 175 | Construction and Characterization of a 10-fold Genome Equivalent Rat P1-Derived Artificial Chromosome Library | 2.0 | 78 | Citations (PDF) |
| 176 | The Human 2′,5′-Oligoadenylate Synthetase Locus Is Composed of Three Distinct Genes Clustered on Chromosome 12q24.2 Encoding the 100-, 69-, and 40-kDa Forms | 2.0 | 86 | Citations (PDF) |
| 177 | The UTX gene escapes X inactivation in mice and humans. | 2.1 | 253 | Citations (PDF) |
| 178 | Characterisation of an inverted X chromosome (p11.2q21.3) associated with mental retardation using FISH. | 2.2 | 10 | Citations (PDF) |
| 179 | A Golgi Localization Signal Identified in the Menkes Recombinant Protein | 2.1 | 88 | Citations (PDF) |
| 180 | Two Hundred One Consecutive Living-Donor Nephrectomies | 0.0 | 81 | Citations (PDF) |
| 181 | Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene. | 2.1 | 102 | Citations (PDF) |
| 182 | Retrofitting vectors for Escherichia coli-based artificial chromosomes (PACs and BACs) with markers for transfection studies. | 3.2 | 35 | Citations (PDF) |
| 183 | Generalized Seizures Associated with the Use of Muromonab-CD3 in Two Patients after Kidney Transplantation | 1.5 | 7 | Citations (PDF) |
| 184 | A Gene-Based Genetic Linkage and Comparative Map of the Rat X Chromosome | 2.0 | 47 | Citations (PDF) |
| 185 | A Sequence-Ready Physical Map of a Region of 12q24.1 | 2.0 | 10 | Citations (PDF) |
| 186 | Novel Genes Mapping to the Critical Region of the 5q− Syndrome | 2.0 | 20 | Citations (PDF) |
| 187 | Two Members of the HumanGene Family Located in Xp21.3 Are Expressed in Tumors of Various Histological Origins | 2.0 | 122 | Citations (PDF) |
| 188 | Chorea-acanthocytosis: genetic linkage to chromosome 9q21. | 4.5 | 131 | Citations (PDF) |
| 189 | Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16. | 4.5 | 309 | Citations (PDF) |
| 190 | Mutation screening of the EXT1 and EXT2 genes in patients with hereditary multiple exostoses. | 4.5 | 136 | Citations (PDF) |
| 191 | Rejection of hamster skin xenografts by rats in the absence of anti-hamster antibody formation | 1.8 | 2 | Citations (PDF) |
| 192 | USE OF CTLA4-Ig IN COMBINATION WITH CONVENTIONAL IMMUNOSUPPRESSIVE AGENTS TO PROLONG ALLOGRAFT SURVIVAL | 1.7 | 35 | Citations (PDF) |
| 193 | Comparative mapping on the mouse X Chromosome defines a myotubular myopathy equivalent region | 1.3 | 4 | Citations (PDF) |
| 194 | Human genetics: Dissecting Williams syndrome | 2.5 | 16 | Citations (PDF) |
| 195 | A novel point mutation in the mcleod syndrome gene in neuroacanthocytosis | 4.7 | 77 | Citations (PDF) |
| 196 | A molecular defect in loricrin, the major component of the cornified cell envelope, underlies Vohwinkel's syndrome | 14.2 | 248 | Citations (PDF) |
| 197 | MARKED PROLONGATION OF RAT SKIN XENOGRAFTS INDUCED BY INTRATHYMIC INJECTION OF XENOGENEIC SPLENOCYTES AND A SHORT COURSE OF RAPAMYCIN IN ANTILYMPHOCYTE SERUM-TREATED MICE | 1.7 | 18 | Citations (PDF) |
| 198 | Isolation and characterization of a MAGE gene family in the Xp21.3 region. | 5.3 | 94 | Citations (PDF) |
| 199 | Autism, mental retardation, multiple exostoses and short stature in a female with 46,X,t(X;8)(p22.13;q22.1) | 0.6 | 30 | Citations (PDF) |
| 200 | NORMAL PANCREAS ALLOGRAFT FUNCTION FOLLOWING SIMULTANEOUS PANCREAS KIDNEY TRANSPLANTATION AFTER RESCUE THERAPY WITH TACROLIMUS (FK506) | 1.7 | 26 | Citations (PDF) |
| 201 | Two polymorphic dinucleotide repeats in the rat dystrophin gene, including the conserved 3′ UTR repeat | 1.3 | 3 | Citations (PDF) |
| 202 | Kidney Transplantation in Diabetic Patients Using Cyclosporine: Five-Year Follow-up | 0.0 | 28 | Citations (PDF) |
| 203 | Identification of a novel gene, ETX1 from Xp21.1, a candidate gene for X-linked retintis pigmentosa (RP3). | 2.1 | 27 | Citations (PDF) |
| 204 | A Single-Center Experience With Six-Antigen—Matched Kidney Transplants | 0.0 | 9 | Citations (PDF) |
| 205 | Three genes that escape X chromosome inactivation are clustered within a 6 Mb YAC contig and STS map in Xp11.21-p11.22. | 2.1 | 60 | Citations (PDF) |
| 206 | Construction of a YAC contig spanning the Xq13.3 subband | 2.0 | 18 | Citations (PDF) |
| 207 | Assignment of the gene (EPLG2) encoding a high-affinity binding protein for the receptor tyrosine kinase Elk to a 200-kilobasepair region in human chromosome Xq12 | 2.0 | 8 | Citations (PDF) |
| 208 | Characterization of the exon structure of the Menkes disease gene using vectorette PCR | 2.0 | 95 | Citations (PDF) |
| 209 | A High-Resolution Interval Map of the q21 Region of the Human X Chromosome | 2.0 | 19 | Citations (PDF) |
| 210 | High-Resolution Comparative Mapping of the Proximal Region of the Mouse X Chromosome | 2.0 | 22 | Citations (PDF) |
| 211 | Construction of Two YAC Contigs in Human Xp11.23–p11.22, One Encompassing the Loci OATL1,GATA,TFE3, and SYP, the Other Linking DXS255 to DXS146 | 2.0 | 7 | Citations (PDF) |
| 212 | Transplantation | 1.7 | 12 | Citations (PDF) |
| 213 | Transplantation | 1.7 | 2 | Citations (PDF) |
| 214 | INDUCTION OF TOLERANCE TO SKIN ALLOGRAFTS BY INTRATHYMIC INJECTION OF DONOR SPLENOCYTES | 1.7 | 0 | Citations (PDF) |
| 215 | Indefinite Survival Following Small Intestinal Transplantation After Intrathymic Injection Of The Donor With Recipient-Type Splenocytes In A Rat Model | 1.7 | 0 | Citations (PDF) |
| 216 | X linked Charcot-Marie-Tooth disease (CMTX1): a study of 15 families with 12 highly informative polymorphisms. | 2.2 | 20 | Citations (PDF) |
| 217 | Mutations in the connexin 32 gene in X-linked dominant Charcot-Marie-Tooth disease (CMTX1) | 2.1 | 199 | Citations (PDF) |
| 218 | A 2.8 Mb YAC contig in 11q12-q13 localizes candidate genes for atopy: Fc epsilon RI beta and CD20. | 2.1 | 27 | Citations (PDF) |
| 219 | Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia. | 2.1 | 75 | Citations (PDF) |
| 220 | X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions. | 2.1 | 41 | Citations (PDF) |
| 221 | YACs, BACs, PACs and MACs: Artificial chromosomes as research tools | 8.1 | 160 | Citations (PDF) |
| 222 | An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita | 31.8 | 825 | Citations (PDF) |
| 223 | Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism | 31.8 | 754 | Citations (PDF) |
| 224 | Gene deletion causing adrenal hypoplasia congenita and hypogonadotrophic hypogonadism | 1.5 | 10 | Citations (PDF) |
| 225 | Isolation of the gene for McLeod syndrome that encodes a novel membrane transport protein | 23.8 | 284 | Citations (PDF) |
| 226 | Isolation of genes from cloned DNA | 2.4 | 6 | Citations (PDF) |
| 227 | Identification of YAC and Cosmid Clones Encompassing the ZFX-POLA Region Using Irradiation Hybrid Cell Lines | 2.0 | 6 | Citations (PDF) |
| 228 | A 2-Mb YAC Contig Encompassing Three Loci (DXF34, DXS14, and DXS390) That Lie between Xp11.2 Translocation Breakpoints Associated with Incontinentia Pigmenti Type 1 | 2.0 | 9 | Citations (PDF) |
| 229 | Physical Mapping in a YAC Contig of 11 Markers on the Human X Chromosome in Xp11.23 | 2.0 | 14 | Citations (PDF) |
| 230 | Analysis of , the Murine Homologue of the Locus for Menkes Disease, in Normal and Mottled () Mice | 2.0 | 28 | Citations (PDF) |
| 231 | DXS106 and DXS559 Flank the X-Linked Dystonia-Parkinsonism Syndrome Locus (DYT3) | 2.0 | 38 | Citations (PDF) |
| 232 | Identification of a yeast artificial chromosome (YAC) spanning the synovial sarcoma-specific t(X;18)(p11.2;q11.2) breakpoint | 1.6 | 32 | Citations (PDF) |
| 233 | Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein | 14.2 | 740 | Citations (PDF) |
| 234 | The Isolation of cDNAs from OATL1 at Xp11.2 Using a 480-kb YAC | 2.0 | 20 | Citations (PDF) |
| 235 | Methods of Inducing Immunological Tolerance to Tissue Allografts and Xenografts | 0.7 | 0 | Citations (PDF) |
| 236 | Identification of a yeast artificial chromosome that spans the human papillary renal cell carcinoma-associated t(X;1) breakpoint in Xp11.2. | 1.6 | 11 | Citations (PDF) |
| 237 | Primers for the dinucleotide repeat at the DXS453 locus also recognizes the DXS983 locus. | 2.1 | 1 | Citations (PDF) |
| 238 | Dinucleotide repeat polymorphisms from DXS106 and DXS227 YACs using a two stage approach. | 2.1 | 8 | Citations (PDF) |
| 239 | The utrophin and dystrophin genes share similarities in genomic structure. | 2.1 | 97 | Citations (PDF) |
| 240 | Four dinucleotide repeat polymorphisms at the D7S804 locus. | 2.1 | 1 | Citations (PDF) |
| 241 | 2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes. | 2.1 | 58 | Citations (PDF) |
| 242 | MINIMUM NUMBER OF ISLETS REQUIRED TO MAINTAIN EUGLYCEMIA AND THEIR REDUCED IMMUNOGENICITY AFTER TRANSPLANTATION INTO DIABETIC MICE | 1.7 | 15 | Citations (PDF) |
| 243 | Isolation of the human Xp21 glycerol kinase gene by positional cloning. | 2.1 | 43 | Citations (PDF) |
| 244 | Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA). | 2.1 | 11 | Citations (PDF) |
| 245 | A contig of non-chimaeric YACs containing the spinal muscular atrophy gene in 5q13. | 2.1 | 73 | Citations (PDF) |
| 246 | Fine mapping of the human SCIDX1 locus at Xq12-13.1. | 2.1 | 20 | Citations (PDF) |
| 247 | Characterization of a YAC containing part or all of the Norrie disease locus. | 2.1 | 12 | Citations (PDF) |
| 248 | Characterization of a 1.0 Mb YAC contig spanning two chromosome breakpoints related to Menkes disease. | 2.1 | 34 | Citations (PDF) |
| 249 | Reconstruction of the 2.4 Mb human DMD-gene by homologous YAC recombination. | 2.1 | 99 | Citations (PDF) |
| 250 | A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genes. | 2.1 | 33 | Citations (PDF) |
| 251 | Localization of the synovial sarcoma t(X;18)(p11.2;q11.2) breakpoint by fluorescence in situ hybridization. | 2.1 | 40 | Citations (PDF) |
| 252 | Distal transcript of the dystrophin gene initiated from an alternative first exon and encoding a 75-kDa protein widely distributed in nonmuscle tissues. | 5.3 | 146 | Citations (PDF) |
| 253 | Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters. | 2.1 | 260 | Citations (PDF) |
| 254 | A yeast artificial chromosome contig containing the complete Duchenne muscular dystrophy gene | 2.0 | 76 | Citations (PDF) |
| 255 | Fine-mapping of the spinal muscular atrophy locus to a region flanked by MAP1B and D5S6 | 2.0 | 30 | Citations (PDF) |
| 256 | Preoperative evaluation for diabetic renal transplantation: Impact of clinical, laboratory, and echocardiographic parameters on patient and allograft survival | 1.6 | 29 | Citations (PDF) |
| 257 | Characterization of a yeast artificial chromosome contig spanning the Huntington's disease gene candidate region | 14.2 | 71 | Citations (PDF) |
| 258 | Isolation of a candidate gene for Norrie disease by positional cloning | 14.2 | 253 | Citations (PDF) |
| 259 | Complete coverage of the Schizosaccharomyces pombe genome in yeast artificial chromosomes | 14.2 | 99 | Citations (PDF) |
| 260 | Replication errors may contribute to the generation of large deletions and duplications in the dystrophin gene | 1.0 | 4 | Citations (PDF) |
| 261 | Isolation of the human sex determining region from a Y-enriched yeast artificial chromosome library | 2.0 | 8 | Citations (PDF) |
| 262 | CHARACTERIZATION OF SPLEEN CELLS CAPABLE OF INDUCING UNRESPONSIVENESS IN ALS-TREATED MICE | 1.7 | 21 | Citations (PDF) |
| 263 | EFFECT OF GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR ON THE INDUCTION OF UNRESPONSIVENESS BY LYMPHOID CELLS | 1.7 | 14 | Citations (PDF) |
| 264 | PREVENTION OF GRAFT-VERSUS-HOST DISEASE FOLLOWING SMALL BOWEL TRANSPLANTATION WITH POLYCLONAL AND MONOCLONAL ANTILYMPHOCYTE SERUM | 1.7 | 26 | Citations (PDF) |
| 265 | Mapping irradiation hybrids to cosmid and yeast artificial chromosome libraries by direct hybridization of Alu-PCR products. | 11.2 | 47 | Citations (PDF) |
| 266 | Cloning of the HLA class II region in yeast artificial chromosomes. | 5.3 | 40 | Citations (PDF) |
| 267 | Molecular cloning and analysis of the fragile X region in man. | 11.2 | 50 | Citations (PDF) |
| 268 | A dinucleotide repeat polymorphism at the DMD locus. | 11.2 | 17 | Citations (PDF) |
| 269 | Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: their potential use as reference libraries. | 5.3 | 164 | Citations (PDF) |
| 270 | Yeast artificial chromosome libraries containing large inserts from mouse and human DNA. | 5.3 | 347 | Citations (PDF) |
| 271 | Complications Associated with Immunosuppressive Therapy and Their Management | 2.3 | 37 | Citations (PDF) |
| 272 | A Randomized Clinical Trial of Prophylactic OKT3 Monoclonal Antibody in Liver Allograft Recipients | 0.0 | 41 | Citations (PDF) |
| 273 | Dystrophin expression and genotypic analysis of two cases of benign X linked myopathy (McLeod's syndrome). | 2.2 | 16 | Citations (PDF) |
| 274 | Dystrophin, the protein product of the Duchenne/Becker muscular dystrophy gene | 7.4 | 54 | Citations (PDF) |
| 275 | SUCCESSFUL TREATMENT OF EXPERIMENTAL DIABETES BY SEQUENTIAL TRANSPLANTATIONS OF MULTIPLE-DONOR PANCREATIC ISLET ALLOGRAFTS | 1.7 | 7 | Citations (PDF) |
| 276 | GRAFT-VERSUS-HOST DISEASE IN FULLY ALLOGENEIC SMALL BOWEL TRANSPLANTATION IN THE RAT | 1.7 | 25 | Citations (PDF) |
| 277 | The Duchenne and Becker muscular dystrophy gene and protein product dystrophin | 1.4 | 2 | Citations (PDF) |
| 278 | PROLONGATION OF SKIN ALLOGRAFT SURVIVAL IN ANTILYMPHOCYTE SERUM-TREATED MICE BY POSTTRANSPLANT ADMINISTRATION OF PERIPHERAL BLOOD LYMPHOCYTES | 1.7 | 4 | Citations (PDF) |
| 279 | Development of clinical immunosuppression for organ transplantation | 0.2 | 0 | Citations (PDF) |
| 280 | An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus | 2.0 | 1,203 | Citations (PDF) |
| 281 | The complete sequence of dystrophin predicts a rod-shaped cytoskeletal protein | 23.8 | 1,568 | Citations (PDF) |
| 282 | A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene | 2.0 | 120 | Citations (PDF) |
| 283 | STUDIES IN SMALL BOWEL TRANSPLANTATION | 1.7 | 43 | Citations (PDF) |
| 284 | INDUCTION OF ANTIGEN-SPECIFIC UNRESPONSIVENESS TO PANCREATIC ISLET ALLOGRAFTS BY ANTILYMPHOCYTE SERUM | 1.7 | 13 | Citations (PDF) |
| 285 | EFFECT OF BLOOD TRANSFUSION ON IL-2 PRODUCTION | 1.7 | 43 | Citations (PDF) |
| 286 | Lactobacillus: An Unusual Case of Splenic Abscess and Sepsis in an Immunocompromised Host | 0.4 | 29 | Citations (PDF) |
| 287 | REPRODUCIBLE HIGH YIELD OF RAT ISLETS BY STATIONARY IN VITRO DIGESTION FOLLOWING PANCREATIC DUCTAL OR PORTAL VENOUS COLLAGENASE INJECTION1 | 1.7 | 222 | Citations (PDF) |
| 288 | THE ACQUIRED IMMUNODEFICIENCY SYNDROME AND TRANSPLANTATION | 1.7 | 87 | Citations (PDF) |
| 289 | EFFECT OF POSTTRANSPLANTATION ADMINISTRATION OF PERIPHERAL BLOOD LYMPHOCYTES IN SKIN-GRAFTED MICE TREATED WITH ANTILYMPHOCYTE SERUM OR ANTILYMPHOCYTE SERUM PLUS BONE MARROW | 1.7 | 4 | Citations (PDF) |
| 290 | Infectious complications with the use of cyclosporine versus azathioprine after cadaveric kidney transplantation | 1.3 | 27 | Citations (PDF) |
| 291 | Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals. | 23.8 | 2,426 | Citations (PDF) |
| 292 | A small deletion in the Duchenne/Becker muscular dystrophy locus —a functionally important region? | 1.9 | 6 | Citations (PDF) |
| 293 | A giant locus for the Duchenne and Becker muscular dystrophy gene | 7.6 | 94 | Citations (PDF) |
| 294 | Regional localization of the murine Duchenne muscular dystrophy gene on the mouse X chromosome | 1.3 | 45 | Citations (PDF) |
| 295 | A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome | 23.8 | 156 | Citations (PDF) |
| 296 | IMMUNE REACTIVITY IN CONGENIC MICE AFTER ALLOGENEIC OR ISOGENEIC TRANSFUSION | 1.7 | 11 | Citations (PDF) |
| 297 | IMMUNOLOGICAL CHARACTERISTICS OF PURIFIED PANCREATIC ISLET GRAFTS | 1.7 | 79 | Citations (PDF) |
| 298 | DNA linkage analysis of X chromosome-linked chronic granulomatous disease. | 5.3 | 103 | Citations (PDF) |
| 299 | Cloning the gene for an inherited human disorder—chronic granulomatous disease—on the basis of its chromosomal location | 31.8 | 851 | Citations (PDF) |
| 300 | Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy | 31.8 | 487 | Citations (PDF) |
| 301 | Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene | 31.8 | 1,102 | Citations (PDF) |
| 302 | Renal transplantation in the diabetic | 1.2 | 8 | Citations (PDF) |
| 303 | Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families. | 2.2 | 36 | Citations (PDF) |
| 304 | Specific cloning of DNA fragments absent from the DNA of a male patient with an X chromosome deletion. | 5.3 | 435 | Citations (PDF) |
| 305 | INDUCTION OF GRAFT-VERSUS-HOST DISEASE BY SMALL INTESTINAL ALLOTRANSPLANTATION IN RATS | 1.7 | 22 | Citations (PDF) |
| 306 | AN IMPROVED METHOD FOR ISOLATION OF MOUSE PANCREATIC ISLETS | 1.7 | 521 | Citations (PDF) |
| 307 | Detection of deletions spanning the Duchenne muscular dystrophy locus using a tightly linked DNA segment | 31.8 | 404 | Citations (PDF) |
| 308 | Construction of a human X-chromosome-enriched phage library which facilitates analysis of specific loci | 1.6 | 44 | Citations (PDF) |
| 309 | Comparison of kidney transplant survival between patients treated with cyclosporine and those treated with azathioprine and antithymocyte globulin | 1.3 | 20 | Citations (PDF) |
| 310 | INDUCTION OF UNRESPONSIVENESS TO SKIN ALLOGRAFTS IN ADULT MICE DISPARATE AT DEFINED REGIONS OF THE H-2 COMPLEX | 1.7 | 14 | Citations (PDF) |
| 311 | INDUCTION OF UNRESPONSIVENESS TO SKIN ALLOGRAFTS IN ADULT MICE DISPARATE AT DEFINED REGIONS OF THE H-2 COMPLEX | 1.7 | 11 | Citations (PDF) |
| 312 | Antithymocyte globulin, pretransplant blood transfusion, and tissue typing in cadaver kidney transplantation | 1.3 | 9 | Citations (PDF) |
| 313 | Pancreas divisumResults of surgical intervention | 1.3 | 53 | Citations (PDF) |
| 314 | THE EFFECT OF TIMING OF MULTIPLE DONOR-SPECIFIC OR NONSPECIFIC BLOOD TRANSFUSIONS ON SKIN ALLOGRAFT SURVIVAL IN ALS-TREATED MICE | 1.7 | 9 | Citations (PDF) |
| 315 | Antilymphocyte Globulin: A Clinical Transplantation Research Opportunity | 1.0 | 13 | Citations (PDF) |
| 316 | Amphetamine-induced overeating and overweight in rats | 3.8 | 7 | Citations (PDF) |
| 317 | SUPPRESSOR CELLS IN MICE BEARING INTACT SKIN ALLOGRAFTS AFTER BLOOD TRANSFUSIONS | 1.7 | 31 | Citations (PDF) |
| 318 | PROLONGATION OF SKIN ALLOGRAFT SURVIVAL IN H-2 K AND I REGION-INCOMPATIBLE MICE BY PRETRANSPLANT BLOOD TRANSFUSION | 1.7 | 21 | Citations (PDF) |
| 319 | PROLONGATION OF SKIN ALLOGRAFT SURVIVAL IN IMMUNOSUPPRESSED MICE BY MULTIPLE TRANSFUSIONS OF NONSPECIFIC BLOOD | 1.7 | 13 | Citations (PDF) |
| 320 | EFFECT OF A SINGLE TRANSFUSION OF DONOR-SPECIFIC AND NONSPECIFIC BLOOD ON SKIN ALLOGRAFT SURVIVAL IN MICE | 1.7 | 24 | Citations (PDF) |
| 321 | Recurrence of Wegener's granulomatosis after kidney transplantationSuccessful re-induction of remission with cyclophosphamide | 1.6 | 53 | Citations (PDF) |
| 322 | Synergy between spleen cells and bone marrow cells in mixed lymphocyte culture-induced cytotoxicity | 1.5 | 0 | Citations (PDF) |
| 323 | Mycotic Wound Infections: A New Challenge for the Surgeon | 0.0 | 24 | Citations (PDF) |
| 324 | SUPPRESSOR CELLS IN SPECIFIC UNRESPONSIVENESS TO SKIN ALLOGRAFTS IN THYMECTOMIZED, ALS-TREATED, MARROW-INJECTED MICE | 1.7 | 3 | Citations (PDF) |
| 325 | DIFFERENTIAL EFFECT OF CYCLOPHOSPHAMIDE ON STATES OF SPECIFIC ALLOGRAFT UNRESPONSIVENESS IN IMMUNOSUPPRESSED MICE | 1.7 | 6 | Citations (PDF) |
| 326 | BCG immunotherapy: Effects of dose and route of administration on survival of mice bearing established tumors | 1.2 | 2 | Citations (PDF) |
| 327 | THE EFFECT OF TIMING OF SKIN GRAFTS ON SUBSEQUENT SURVIVAL IN ALS-TREATED, MARROW-INFUSED MICE1 | 1.7 | 19 | Citations (PDF) |
| 328 | Immunosuppressive Therapy Following Cryptococcal Meningitis | 1.5 | 6 | Citations (PDF) |
| 329 | Activation of c-type viruses during skin graft rejection in the mouse. Interrelationships between immunostimulation and immunosuppression | 2.8 | 11 | Citations (PDF) |
| 330 | Successful induction of increased resistance to gram-negative bacteria and to endotoxin in immunosuppressed mice | 1.3 | 8 | Citations (PDF) |
| 331 | IMMUNOSUPPRESSIVE EFFECTS OF AN INTERFERON PREPARATION IN VIVO | 1.7 | 65 | Citations (PDF) |
| 332 | STUDIES ON HETEROLOGOUS ANTILYMPHOCYTE SERUM IN MICE | 1.7 | 5 | Citations (PDF) |
| 333 | STUDIES ON HETEROLOGOUS ANTILYMPHOCYTE SERUM IN MICE | 1.7 | 9 | Citations (PDF) |
| 334 | DIFFERENTIAL EFFECT OF ADULT THYMECTOMY IN MICE TREATED WITH ANTILYMPHOCYTE OR ANTITHYMOCYTE SERUM | 1.7 | 2 | Citations (PDF) |
| 335 | Successful treatment of Pneumocystis carinii and Nocardia asteroides in a renal transplant patient | 1.6 | 29 | Citations (PDF) |
| 336 | STUDIES ON HETEROLOGOUS ANTILYMPHOCYTE SERUM IN MICE | 1.7 | 8 | Citations (PDF) |
| 337 | TOLERANCE AFTER TRANSIENTLY PLACED H-2 GRAFTS | 1.7 | 17 | Citations (PDF) |
| 338 | ANTILYMPHOCYTE SERUM AND CELL-FREE ANTIGEN LOADING | 1.7 | 14 | Citations (PDF) |
| 339 | Heterologous Antilymphocyte Serum HETEROLOGOUS ANTILYMPHOCYTE SERA AND SOME OF THEIR EFFECTS | 1.7 | 47 | Citations (PDF) |
| 340 | SOME EFFECTS OF PURIFIED HETEROLOGOUS ANTIHUMAN LYMPHOCYTE SERUM IN MAN | 1.7 | 76 | Citations (PDF) |
| 341 | Emergencies Associated with Clinical Renal Transplantation | 1.2 | 4 | Citations (PDF) |
| 342 | Studies on Heterologous Anti-Lymphocyte Serum in Mice: II. Effect on the Immune Response1 | 0.8 | 135 | Citations (PDF) |
| 343 | PREPARATION OF MURINE TRANSPLANTATION ANTIGENS | 1.7 | 12 | Citations (PDF) |
| 344 | Adenomatous polyps of the stomach. A clinical and pathological study of 153 cases | 2.7 | 95 | Citations (PDF) |
| 345 | Primary cancer of the female urethra | 2.7 | 19 | Citations (PDF) |
| 346 | Human VPS13A is associated with multiple organelles and influences mitochondrial morphology and lipid droplet motility. | 1.0 | 170 | Citations (PDF) |
| 347 | Whole-exome sequencing in children with dyslexia implicates rare variants in CLDN3 and ion channel genes | 1.9 | 1 | Citations (PDF) |
