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Human Genetics Division
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top-articles
Human Genetics Division
138
(top 1%)
papers
9.5K
(top 1%)
citations
53
(top 1%)
h
-index
96
(top 1%)
g
-index
143
all documents
9.9K
doc citations
2.1K
citing journals
Top Articles
#
Title
Journal
Year
Citations
1
Inactivating mutations of the histone methyltransferase gene EZH2 in myeloid disorders
Nature Genetics
2010
1,034
2
Genome-wide association study identifies five loci associated with lung function
Nature Genetics
2010
518
3
Aberrations of
EZH2
in Cancer
Clinical Cancer Research
2011
503
4
In vivo equilibrium of proinflammatory IL-17+ and regulatory IL-10+ Foxp3+ RORγt+ T cells
Journal of Experimental Medicine
2008
491
5
JAK2 haplotype is a major risk factor for the development of myeloproliferative neoplasms
Nature Genetics
2009
365
6
Common variants near CAV1 and CAV2 are associated with primary open-angle glaucoma
Nature Genetics
2010
357
7
C-reactive protein and its role in metabolic syndrome: mendelian randomisation study
Lancet, The
2005
300
8
Phenotypic and functional analyses show stem cell-derived hepatocyte-like cells better mimic fetal rather than adult hepatocytes
Journal of Hepatology
2015
271
9
Subcellular Localization of ALMS1 Supports Involvement of Centrosome and Basal Body Dysfunction in the Pathogenesis of Obesity, Insulin Resistance, and Type 2 Diabetes
Diabetes
2005
212
10
Extent of genome-wide linkage disequilibrium in Australian Holstein-Friesian cattle based on a high-density SNP panel
BMC Genomics
2008
203
11
Lack of Conventional Dendritic Cells Is Compatible with Normal Development and T Cell Homeostasis, but Causes Myeloid Proliferative Syndrome
Immunity
2008
198
12
Dendritic Cells Ameliorate Autoimmunity in the CNS by Controlling the Homeostasis of PD-1 Receptor+ Regulatory T Cells
Immunity
2012
184
13
The first linkage disequilibrium (LD) maps: Delineation of hot and cold blocks by diplotype analysis
Proceedings of the National Academy of Sciences of the United States of America
2002
170
14
Influence of matrix metalloproteinase genotype on cardiovascular disease susceptibility and outcome
Cardiovascular Research
2006
156
15
A maternal hypomethylation syndrome presenting as transient neonatal diabetes mellitus
Human Genetics
2006
147
16
Deletion of chromosome 13 detected by conventional cytogenetics is a critical prognostic factor in myeloma
Leukemia
2006
141
17
Role of the JAK–STAT pathway in myocardial injury
Trends in Molecular Medicine
2007
137
18
Molecular profiling of chronic myelomonocytic leukemia reveals diverse mutations in >80% of patients with TET2 and EZH2 being of high prognostic relevance
Leukemia
2011
131
19
The Early Human Germ Cell Lineage Does Not Express SOX2 During In Vivo Development or upon In Vitro Culture1
Biology of Reproduction
2008
116
20
Proteome‐wide analyses of human hepatocytes during differentiation and dedifferentiation
Hepatology
2013
113
21
Loss of Caspase-8 Protects Mice Against Inflammation-Related Hepatocarcinogenesis but Induces Non-Apoptotic Liver Injury
Gastroenterology
2011
105
22
13q deletion anatomy and disease progression in patients with chronic lymphocytic leukemia
Leukemia
2011
104
23
Haplotypic analysis of the MMP-9 gene in relation to coronary artery disease
Journal of Molecular Medicine
2003
97
24
Centriolar Association of ALMS1 and Likely Centrosomal Functions of the ALMS Motif–containing Proteins C10orf90 and KIAA1731
Molecular Biology of the Cell
2010
97
25
King–Denborough syndrome with and without mutations in the skeletal muscle ryanodine receptor (RYR1) gene
Neuromuscular Disorders
2011
97
26
Different autonomous myogenic cell populations revealed by ablation of Myf5-expressing cells during mouse embryogenesis
Development (Cambridge)
2008
93
27
The JAK2 46/1 haplotype predisposes to MPL-mutated myeloproliferative neoplasms
Blood
2010
93
28
Characterization and Multipotentiality of Human Fetal Femur-Derived Cells: Implications for Skeletal Tissue Regeneration
Stem Cells
2006
92
29
Properties of linkage disequilibrium (LD) maps
Proceedings of the National Academy of Sciences of the United States of America
2002
89
30
Identification of a novel gene,
FGFR1OP2
, fused to
FGFR1
in 8p11 myeloproliferative syndrome
Genes Chromosomes and Cancer
2004
89
31
The t(8;17)(p11;q23) in the 8p11 myeloproliferative syndrome fuses MYO18A to FGFR1
Leukemia
2005
85
32
Standardisation of molecular monitoring for chronic myeloid leukaemia
Best Practice and Research in Clinical Haematology
2009
85
33
IL-13 receptor α 2: A regulator of IL-13 and IL-4 signal transduction in primary human fibroblasts
Journal of Allergy and Clinical Immunology
2006
84
34
Differences in Matrix Metalloproteinase-1 and Matrix Metalloproteinase-12 Transcript Levels Among Carotid Atherosclerotic Plaques With Different Histopathological Characteristics
Stroke
2004
83
35
Association of Tumor Necrosis Factor-α Polymorphisms and Ozone-induced Change in Lung Function
American Journal of Respiratory and Critical Care Medicine
2005
80
36
The histone deacetylase inhibitors vorinostat and romidepsin downmodulate IL‐10 expression in cutaneous T‐cell lymphoma cells
British Journal of Pharmacology
2011
78
37
Haplotype Effect of the Matrix Metalloproteinase-1 Gene on Risk of Myocardial Infarction
Circulation Research
2005
77
38
Variation in the toll-like receptor 4 gene and susceptibility to myocardial infarction
Pharmacogenetics and Genomics
2005
75
39
A map of the human genome in linkage disequilibrium units
Proceedings of the National Academy of Sciences of the United States of America
2005
75
40
The role of Toll-like receptors and related receptors of the innate immune system in asthma
Current Opinion in Allergy and Clinical Immunology
2006
75
41
Reduced secretion of fibulin 5 in age-related macular degeneration and cutis laxa
Human Mutation
2006
73
42
Timing of acquisition of deletion 13 in plasma cell dyscrasias is dependent on genetic context
Haematologica
2009
68
43
Effects of Polyclonal IgG Derived from Patients with Different Clinical Types of the Antiphospholipid Syndrome on Monocyte Signaling Pathways
Journal of Immunology
2010
67
44
Free radical scavenging inhibits STAT phosphorylation following in vivo ischemia/reperfusion injury
FASEB Journal
2006
66
45
Frequent upregulation of
MYC
in plasma cell leukemia
Genes Chromosomes and Cancer
2009
65
46
Urocortin prevents mitochondrial permeability transition in response to reperfusion injury indirectly by reducing oxidative stress
American Journal of Physiology - Heart and Circulatory Physiology
2007
60
47
Host Cytokine Genotype is Related to Adverse Prognosis and Systemic Inflammation in Gastro-Oesophageal Cancer
Annals of Surgical Oncology
2007
60
48
EGF
+61 gene polymorphism and susceptibility to and prognostic markers in cutaneous malignant melanoma
International Journal of Cancer
2003
59
49
Haplotypic analyses of the IGF2-INS-TH gene cluster in relation to cardiovascular risk traits
Human Molecular Genetics
2004
57
50
Feeding a protein-restricted diet during pregnancy induces altered epigenetic regulation of peroxisomal proliferator-activated receptor-α in the heart of the offspring
Journal of Developmental Origins of Health and Disease
2011
57
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