Articoli con mandati relativi all'accesso pubblico - gil atzmonUlteriori informazioni
TotaleNIHMRCWellcomeNIHRBHFNSFSwedish Research CouncilParkinson's Foundation, USAEuropean CommissionBMBFVACIHRAcademy of FinlandNWOBBSRCGovernment of SpainHFSPNHMRCDFGDFFNMRCResearch Grants Council, Hong KongLUNGevity Foundation, USAJDRFSNSFHHMIGenome CanadaHelmholtzFORTECSOESRCAction on Hearing Loss, UKNational Research Foundation, SingaporeLeducq Foundation, USADoDAHAFNRSFWODCTITekesINSERMCSIRKnut and Alice Wallenberg FoundationA*StarEPSRCZonMwDoris Duke Charitable FoundationState of CalifoniaGoverno ItalianoAXA Research Fund, FranceHealth Data Research, UKMinistry of Health, Singapore
Non disponibile pubblicamente: 1
Cadherin and Protocadherin Genes Implicated by Novel Ultra-Rare Variants in Schizophrenia Cases From a Founder Population
T Lencz, J Yu, R Khan, M Lam, G Atzmon, I Pe'er
Biological Psychiatry 87 (9), S112-S113, 2020
Mandati: US National Institutes of Health
Disponibili pubblicamente: 127
Age-related clonal hematopoiesis associated with adverse outcomes
S Jaiswal, P Fontanillas, J Flannick, A Manning, PV Grauman, BG Mar, ...
New England Journal of Medicine 371 (26), 2488-2498, 2014
Mandati: US National Institutes of Health, UK Medical Research Council, Wellcome Trust
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
Sequence variants in SLC16A11 are a common risk factor for type 2 diabetes in Mexico
AL Williams, SBR Jacobs, H Moreno-Macías, A Huerta-Chagoya, ...
Nature 506 (7486), 97-101, 2014
Mandati: US National Institutes of Health, Wellcome Trust
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes
J Flannick, G Thorleifsson, NL Beer, SBR Jacobs, N Grarup, NP Burtt, ...
Nature genetics 46 (4), 357-363, 2014
Mandati: US National Institutes of Health, Danish Council for Independent Research …
Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: a soft clustering analysis
MS Udler, J Kim, M von Grotthuss, S Bonàs-Guarch, JB Cole, J Chiou, ...
PLoS medicine 15 (9), e1002654, 2018
Mandati: US National Institutes of Health, UK Medical Research Council
Association of common genetic variation in the insulin/IGF1 signaling pathway with human longevity
L Pawlikowska, D Hu, S Huntsman, A Sung, C Chu, J Chen, AH Joyner, ...
Aging cell 8 (4), 460-472, 2009
Mandati: US National Institutes of Health
Functional variants in the LRRK2 gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease
KY Hui, H Fernandez-Hernandez, J Hu, A Schaffner, N Pankratz, NY Hsu, ...
Science translational medicine 10 (423), eaai7795, 2018
Mandati: US National Science Foundation, US National Institutes of Health, UK Medical …
Genetic variation in human telomerase is associated with telomere length in Ashkenazi centenarians
G Atzmon, M Cho, RM Cawthon, T Budagov, M Katz, X Yang, G Siegel, ...
Proceedings of the National Academy of Sciences 107 (suppl_1), 1710-1717, 2010
Mandati: US National Institutes of Health
Extreme longevity is associated with increased serum thyrotropin
G Atzmon, N Barzilai, JG Hollowell, MI Surks, I Gabriely
The Journal of Clinical Endocrinology & Metabolism 94 (4), 1251-1254, 2009
Mandati: US National Institutes of Health
Interrogating the genetic determinants of Tourette’s syndrome and other tic disorders through genome-wide association studies
D Yu, JH Sul, F Tsetsos, MS Nawaz, AY Huang, I Zelaya, C Illmann, ...
American Journal of Psychiatry 176 (3), 217-227, 2019
Mandati: US Department of Defense, US National Institutes of Health, German Research …
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls
J Flannick, JM Mercader, C Fuchsberger, MS Udler, A Mahajan, J Wessel, ...
Nature 570 (7759), 71-76, 2019
Mandati: US National Institutes of Health, US Department of Veterans Affairs …
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
N Barban, R Jansen, R De Vlaming, A Vaez, JJ Mandemakers, FC Tropf, ...
Nature genetics 48 (12), 1462-1472, 2016
Mandati: US National Science Foundation, US National Institutes of Health, US …
Abraham's children in the genome era: major Jewish diaspora populations comprise distinct genetic clusters with shared Middle Eastern Ancestry
G Atzmon, L Hao, I Pe'er, C Velez, A Pearlman, PF Palamara, B Morrow, ...
The American Journal of Human Genetics 86 (6), 850-859, 2010
Mandati: US National Institutes of Health
A meta-analysis of genome-wide association studies identifies multiple longevity genes
J Deelen, DS Evans, DE Arking, N Tesi, M Nygaard, X Liu, MK Wojczynski, ...
Nature communications 10 (1), 3669, 2019
Mandati: US National Institutes of Health, UK Medical Research Council, National …
Humanin: a novel central regulator of peripheral insulin action
RH Muzumdar, DM Huffman, G Atzmon, C Buettner, LJ Cobb, S Fishman, ...
PloS one 4 (7), e6334, 2009
Mandati: US National Institutes of Health
Tissue‐specific dysregulation of DNA methylation in aging
RF Thompson, G Atzmon, C Gheorghe, HQ Liang, C Lowes, JM Greally, ...
Aging cell 9 (4), 506-518, 2010
Mandati: US National Institutes of Health
Low insulin‐like growth factor‐1 level predicts survival in humans with exceptional longevity
S Milman, G Atzmon, DM Huffman, J Wan, JP Crandall, P Cohen, ...
Aging cell 13 (4), 769-771, 2014
Mandati: US National Institutes of Health
Visceral adipose tissue modulates mammalian longevity
R Muzumdar, DB Allison, DM Huffman, X Ma, G Atzmon, FH Einstein, ...
Aging cell 7 (3), 438-440, 2008
Mandati: US National Institutes of Health
Gene flow from North Africa contributes to differential human genetic diversity in southern Europe
LR Botigué, BM Henn, S Gravel, BK Maples, CR Gignoux, E Corona, ...
Proceedings of the National Academy of Sciences 110 (29), 11791-11796, 2013
Mandati: US National Institutes of Health, Government of Spain
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