181(top 2%)
papers
7.4K(top 1%)
citations
52(top 1%)
h-index
87(top 1%)
g-index
314
all documents
8.6K
doc citations
2.4K
citing journals

Top Articles

#TitleJournalYearCitations
1Interventions to Slow Aging in Humans: Are We Ready?Aging Cell2015466
2Practical aspects of imputation-driven meta-analysis of genome-wide association studiesHuman Molecular Genetics2008436
3Gold Nanocomposite Bioink for Printing 3D Cardiac ConstructsAdvanced Functional Materials2017310
4AutismLancet, The2003258
5SIRT2 induces the checkpoint kinase BubR1 to increase lifespanEMBO Journal2014202
6Blood–Brain Barrier Dysfunction in a 3D In Vitro Model of Alzheimer's DiseaseAdvanced Science2019196
7Multiethnic polygenic risk scores improve risk prediction in diverse populationsGenetic Epidemiology2017194
8Biological membranes in EV biogenesis, stability, uptake, and cargo transfer: an ISEV position paper arising from the ISEV membranes and EVs workshopJournal of Extracellular Vesicles2019183
9(CAG)n-hairpin DNA binds to Msh2–Msh3 and changes properties of mismatch recognitionNature Structural and Molecular Biology2005181
10Mucinous Differentiation Correlates with Absence of EGFR Mutation and Presence of KRAS Mutation in Lung Adenocarcinomas with Bronchioloalveolar FeaturesJournal of Molecular Diagnostics2007180
11Exosomes and Nanoengineering: A Match Made for Precision TherapeuticsAdvanced Materials2020165
12Kabuki syndrome: international consensus diagnostic criteriaJournal of Medical Genetics2019151
13Lactobacillus gallinarummodulates the gut microbiota and produces anti-cancer metabolites to protect against colorectal tumourigenesisGut2022151
14Mutations of immunoglobulin transmembrane and cytoplasmic domains: Effects on intracellular signaling and antigen presentationCell1990143
15Causal roles of mitochondrial dynamics in longevity and healthy agingEMBO Reports2019135
16Response to Treatment and Survival of Patients with Non-Small Cell Lung Cancer Undergoing SomaticEGFRMutation TestingOncologist2007134
17Communicating Genetic Risk Information for Common Disorders in the Era of Genomic MedicineAnnual Review of Genomics and Human Genetics2013130
18Mutation in Rpa1 results in defective DNA double-strand break repair, chromosomal instability and cancer in miceNature Genetics2005129
19Adipokine FABP4 integrates energy stores and counterregulatory metabolic responsesJournal of Lipid Research2019127
20Secretion of fatty acid binding protein aP2 from adipocytes through a nonclassical pathway in response to adipocyte lipase activityJournal of Lipid Research2015123
21Fabrication and Mechanical Properties of Engineered Protein‐Based Adhesives and FibersAdvanced Materials2020121
22Onset of Abnormal Blood and Lymphatic Vessel Function and Interstitial Hypertension in Early Stages of CarcinogenesisCancer Research2006116
23Gene expression defines natural changes in mammalian lifespanAging Cell2015113
24Mouse models for human DNA mismatch-repair gene defectsTrends in Molecular Medicine2002109
25Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factorEuropean Journal of Human Genetics2009107
26Localization of the huntington's disease gene to a small segment of chromosome 4 flanked by D4S10 and the telomereCell1987102
27Participation of mouse DNA polymerase   in strand-biased mutagenic bypass of UV photoproducts and suppression of skin cancerProceedings of the National Academy of Sciences of the United States of America2006100
28Comparative proteomic and transcriptomic profiling of the fission yeast Schizosaccharomyces pombeMolecular Systems Biology200792
29Molecular Genetics and EconomicsJournal of Economic Perspectives201190
30Increased Susceptibility to UV-Induced Skin Carcinogenesis in Polymerase η–deficient MiceCancer Research200685
31Hepatocyte Deletion of Triglyceride‐Synthesis Enzyme Acyl CoA: Diacylglycerol Acyltransferase 2 Reduces Steatosis Without Increasing Inflammation or Fibrosis in MiceHepatology201983
32Identification ofKIF21AMutations as a Rare Cause of Congenital Fibrosis of the Extraocular Muscles Type 3 (CFEOM3)200481
33m TORC 2‐ SGK ‐1 acts in two environmentally responsive pathways with opposing effects on longevityAging Cell201474
34Epidermal Growth Factor Receptor Mutation Testing in the Care of Lung Cancer Patients: Fig. 1.Clinical Cancer Research200672
35Genomewide meta‐analysis identifies loci associated with IGF ‐I and IGFBP ‐3 levels with impact on age‐related traitsAging Cell201672
36Three‐Dimensional Models of the Human Brain Development and DiseasesAdvanced Healthcare Materials201870
37A gender-moderated effect of a functionalCOMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome)American Journal of Medical Genetics Part B: Neuropsychiatric Genetics200667
38A common mitochondrial haplogroup is associated with elevated total serum IgE levelsJournal of Allergy and Clinical Immunology200766
39Bioinks and Bioprinting Strategies for Skeletal Muscle Tissue EngineeringAdvanced Materials202266
40Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndromeNeurogenetics200665
41Neurofibromatosis Type 1 in Genetic Counseling Practice: Recommendations of the National Society of Genetic CounselorsJournal of Genetic Counseling200764
42Cytometric profiling in multiple sclerosis uncovers patient population structure and a reduction of CD8low cellsBrain200862
43The Human Variome ProjectScience200858
44Comparative Proteomic Analysis of the PhoP Regulon in Salmonella enterica Serovar Typhi Versus TyphimuriumPLoS ONE200956
45Risk Factors for Early‐Onset Ischemic Stroke: A Case‐Control StudyJournal of the American Heart Association201856
46Turning off the inflammatory, but not the metabolic, flamesNature Medicine201355
47Alveolar progenitor cells and the origin of lung cancerJournal of Internal Medicine202155
48Presenilin/γ‐secretase activity regulates protein clearance from the endocytic recycling compartmentFASEB Journal200654
49Gain‐of‐function mutations in SMAD4 cause a distinctive repertoire of cardiovascular phenotypes in patients with Myhre syndromeAmerican Journal of Medical Genetics, Part A201654
50In genetic control of disease, does 'race' matter?Nature Genetics200453