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Our major interest is in rare mutations that predispose to common diseases, whether their effects are on aneurysm risk, food intake, energy expenditure or body growth (like the Weaver syndrome gene EZH2 and the Cohen-Gibson syndrome gene EED).
By studying rare human genetic disorders like Weaver syndrome, Cohen-Gibson syndrome, paired with data from animal models of obesity and leanness, we hope to derive valuable lessons that are relevant to common disease risk in the general population.
Our major interest is in rare mutations that predispose to common diseases, whether their effects are on aneurysm risk, food intake, energy expenditure or body growth (like the Weaver syndrome gene EZH2 and the Cohen-Gibson syndrome gene EED).
By studying rare human genetic disorders like Weaver syndrome, Cohen-Gibson syndrome, paired with data from animal models of obesity and leanness, we hope to derive valuable lessons that are relevant to common disease risk in the general population.
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论文共 125 篇作者统计合作学者相似作者
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biorxiv(2024)
Mark A. Colijn,Prescilla Carrion,Guillaume Poirier-Morency,Sanja Rogic,Ivan Torres,Mahesh Menon,Michelle Lisonek,Courtney Cook, Ashley DeGraaf, Subramanya Ponnachana Thammaiah, Harish Neelakant, Veerle Willaeys,
PROGRESS IN NEURO-PSYCHOPHARMACOLOGY & BIOLOGICAL PSYCHIATRY (2024): 110888-110888
SCIENCE ADVANCESno. 48 (2023): eadh2726-eadh2726
EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 242-242
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bioRxiv (Cold Spring Harbor Laboratory) (2023)
Developmental cellno. 6 (2023): 489-505.e7
HUMAN MOLECULAR GENETICSno. 15 (2023): 2422-2440
PAEDIATRICS & CHILD HEALTHno. 2 (2023): 107-112
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