Atzmon, Gil
Albert Einstein College of Medicine · University of Haifa
24 papers on CoChatORCID 0000-0001-6895-3607
Most cited papers
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The mutational constraint spectrum quantified from variation in 141,456 humans
Karczewski, K. J., Francioli, L. C., Tiao, G., Cummings, B. B., Alföldi, J., Wang, Q., Collins, R. L., Laricchia, K. M., Ganna, A., Birnbaum, D. P., et al. (2020) · Nature
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 9,434
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Age-related clonal hematopoiesis associated with adverse outcomes
Jaiswal, S., Fontanillas, P., Flannick, J., Manning, A., Grauman, P. V., Mar, B. G., Lindsley, R. C., Mermel, C. H., Burtt, N., Chavez, A., et al. (2014) · New England Journal of Medicine
Acute Myeloid Leukemia ResearchCancer Genomics and Diagnostics
Cited by 4,841
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A genomic mutational constraint map using variation in 76,156 human genomes
Chen, S., Francioli, L. C., Goodrich, J. K., Collins, R. L., Kanai, M., Wang, Q., Alföldi, J., Watts, N. A., Vittal, C., Gauthier, L. D., et al. (2024) · Nature
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 1,727
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The genetic architecture of type 2 diabetes
Fuchsberger, C., Flannick, J., Teslovich, T. M., Mahajan, A., Agarwala, V., Gaulton, K. J., Ma, C., Fontanillas, P., Moutsianas, L., McCarthy, D. J., et al. (2016) · Nature
Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals
Cited by 1,051
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A structural variation reference for medical and population genetics
Collins, R. L., Brand, H., Karczewski, K. J., Zhao, X., Alföldi, J., Francioli, L. C., Khera, A. V., Lowther, C., Gauthier, L. D., Wang, H., et al. (2020) · Nature
Genomic variations and chromosomal abnormalitiesGenomics and Rare Diseases
Cited by 1,037
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Functionally significant insulin-like growth factor I receptor mutations in centenarians
Suh, Y., Atzmon, G., Cho, M.-O., Hwang, D., Liu, B., Leahy, D. J., Barzilai, N., & Cohen, P. (2008) · Proceedings of the National Academy of Sciences
Genetics, Aging, and Longevity in Model OrganismsGrowth Hormone and Insulin-like Growth Factors
Cited by 703
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Removal of Visceral Fat Prevents Insulin Resistance and Glucose Intolerance of Aging
Gabriely, I., Ma, X. H., Yang, X. M., Atzmon, G., Rajala, M. W., Berg, A. H., Scherer, P., Rossetti, L., & Barzilai, N. (2002) · Diabetes
Adipokines, Inflammation, and Metabolic DiseasesAdipose Tissue and Metabolism
Cited by 563
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Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: a soft clustering analysis
Udler, M. S., Kim, J., von Grotthuss, M., Bonàs-Guarch, S., Cole, J. B., Chiou, J., ISGC, C. D. A. O. B. O. M. A. T., Boehnke, M., Laakso, M., Atzmon, G., et al. (2018) · PLOS Medicine
Genetic Associations and EpidemiologyDiabetes and associated disorders
Cited by 542
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Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
Go-T2D Consortium, Flannick, J., T2D-GENES Consortium, Thorleifsson, G., Beer, N. L., Jacobs, S. B. R., Grarup, N., Burtt, N. P., Mahajan, A., Fuchsberger, C., et al. (2014) · Nature Genetics
Genetic Associations and EpidemiologyDiabetes and associated disorders
Cited by 492
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Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies
Yu, D., Sul, J. H., Tsetsos, F., Nawaz, M. S., Huang, A. Y., Zelaya, I., Illmann, C., Osiecki, L., Darrow, S. M., Hirschtritt, M. E., et al. (2019) · American Journal of Psychiatry
Obsessive-Compulsive Spectrum DisordersGenetic Associations and Epidemiology
Cited by 410
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Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease
Hui, K. Y., Fernandez-Hernandez, H., Hu, J., Schaffner, A., Pankratz, N., Hsu, N.-Y., Chuang, L.-S., Carmi, S., Villaverde, N., Li, X., et al. (2018) · Science Translational Medicine
Parkinson's Disease Mechanisms and TreatmentsInflammatory Bowel Disease
Cited by 384
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A meta-analysis of genome-wide association studies identifies multiple longevity genes
Deelen, J., Evans, D. S., Arking, D. E., Tesi, N., Nygaard, M., Liu, X., Wojczynski, M. K., Biggs, M. L., van der Spek, A., Atzmon, G., et al. (2019) · Nature Communications
Genetic Associations and EpidemiologyGenetics, Aging, and Longevity in Model Organisms
Cited by 370
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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
Platform, B. G., Flannick, J., DiscovEHR Collaboration, CHARGE, LuCamp, ProDiGY, GoT2D, ESP, SIGMA-T2D, T2D-GENES, et al. (2019) · Nature
Genetic Associations and EpidemiologyGenomics and Rare Diseases
Cited by 304
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Extreme Longevity Is Associated with Increased Serum Thyrotropin
Atzmon, G., Barzilai, N., Hollowell, J. G., Surks, M. I., & Gabriely, I. (2009) · The Journal of Clinical Endocrinology & Metabolism
Thyroid Disorders and TreatmentsHormonal and reproductive studies
Cited by 260
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Abraham's Children in the Genome Era: Major Jewish Diaspora Populations Comprise Distinct Genetic Clusters with Shared Middle Eastern Ancestry
Atzmon, G., Hao, L., Pe'er, I., Velez, C., Pearlman, A., Palamara, P. F., Morrow, B., Friedman, E., Oddoux, C., Burns, E., et al. (2010) · The American Journal of Human Genetics
Forensic and Genetic ResearchRace, Genetics, and Society
Cited by 260
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Gene flow from North Africa contributes to differential human genetic diversity in southern Europe
Botigué, L. R., Henn, B. M., Gravel, S., Maples, B. K., Gignoux, C. R., Corona, E., Atzmon, G., Burns, E., Ostrer, H., Flores, C., et al. (2013) · Proceedings of the National Academy of Sciences
Forensic and Genetic ResearchGenetic diversity and population structure
Cited by 199
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Sequencing an Ashkenazi reference panel supports population-targeted personal genomics and illuminates Jewish and European origins
Carmi, S., Hui, K. Y., Kochav, E., Liu, X., Xue, J., Grady, F., Guha, S., Upadhyay, K., Ben-Avraham, D., Mukherjee, S., et al. (2014) · Nature Communications
Forensic and Genetic ResearchGenetic Associations and Epidemiology
Cited by 188
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Genetic Predisposition to Elevated Serum Thyrotropin Is Associated with Exceptional Longevity
Atzmon, G., Barzilai, N., Surks, M. I., & Gabriely, I. (2009) · The Journal of Clinical Endocrinology & Metabolism
Thyroid Disorders and TreatmentsGenetic Associations and Epidemiology
Cited by 145
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Genetics, lifestyle and longevity: Lessons from centenarians
Govindaraju, D., Atzmon, G., & Barzilai, N. (2015) · Applied & Translational Genomics
Genetics, Aging, and Longevity in Model OrganismsEvolution and Genetic Dynamics
Cited by 128
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Screening Human Embryos for Polygenic Traits Has Limited Utility
Karavani, E., Zuk, O., Zeevi, D., Barzilai, N., Stefanis, N. C., Hatzimanolis, A., Smyrnis, N., Avramopoulos, D., Kruglyak, L., Atzmon, G., et al. (2019) · Cell
Prenatal Screening and DiagnosticsAssisted Reproductive Technology and Twin Pregnancy
Cited by 111
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The paradox of the insulin/IGF-1 signaling pathway in longevity
Rincon, M., Muzumdar, R. H., Atzmon, G., & Barzilai, N. (2004) · Mechanisms of Ageing and Development
Genetics, Aging, and Longevity in Model OrganismsGrowth Hormone and Insulin-like Growth Factors
Cited by 102
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Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
Rivas, M. A., Avila, B. E., Koskela, J., Huang, H., Stevens, C., Pirinen, M., Haritunians, T., Neale, B. M., Kurki, M., Ganna, A., et al. (2018) · PLoS Genetics
Genomics and Rare DiseasesGenetic Associations and Epidemiology
Cited by 87
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Positive attitude toward life, emotional expression, self-rated health, and depressive symptoms among centenarians and near-centenarians
Kato, K., Zweig, R., Schechter, C. B., Barzilai, N., & Atzmon, G. (2016) · Aging & Mental Health
Aging and Gerontology ResearchAging, Health, and Disability
Cited by 71
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Telomere length is a novel predictive biomarker of sensitivity to anti-EGFR therapy in metastatic colorectal cancer
Augustine, T. A., Baig, M., Sood, A., Budagov, T., Atzmon, G., Mariadason, J. M., Aparo, S., Maitra, R., & Goel, S. (2015) · British Journal of Cancer
Colorectal Cancer Treatments and StudiesTelomeres, Telomerase, and Senescence
Cited by 27
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