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Public Health Genomics and Precision Health Knowledge Base (v10.0)
PHGKB
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Public Health Genomics Branch
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CDC-Authored Genomics and Precision Health Publications Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
CDC-Authored Genomics and Precision Health Publications Database
Last data update: Dec 02, 2024
. (Total: 6432 publications)
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Records 1-7 (of 7 Records)
Query Trace:
Rasooly D[original query]
Epigenome-wide association studies of prenatal maternal mental health and infant epigenetic profiles: a systematic review
Drzymalla E
,
Crider KS
,
Wang A
,
Marta G ,
Khoury MJ
,
Rasooly D
.
Transl Psychiatry 2023 13 (1) 377
Association between a first-degree family history and self-reported personal history of obesity, diabetes, and heart and blood conditions: Results from the All of Us Research Program
Rasooly D
,
Moonesinghe R
,
Littrell K
,
Hull L ,
Khoury MJ
.
J Am Heart Assoc 2023 12 (22) e030779
Family history of arthritis, osteoporosis, and carpal tunnel syndrome and risk of these conditions among U.S. adults
Rasooly D
,
Moonesinghe R
,
Fallon E
,
Barbour KE
,
Khoury MJ
.
Arthritis Care Res (Hoboken) 2024
The Joint Public Health Impact of Family History of Diabetes and Cardiovascular Disease among Adults in the United States: A Population-Based Study.
Rasooly D
,
Yang Q
,
Moonesinghe R
,
Khoury MJ
,
Patel CJ .
Public Health Genomics 2022 1-12
Family History-Wide Association Study ("FamWAS") for Identifying Clinical and Environmental Risk Factors for Common Chronic Diseases.
Rasooly D , Ioannidis JPA ,
Khoury MJ
,
Patel CJ .
Am J Epidemiol 2019 188 (8) 1563-1568
The genomic applications in practice and prevention network.
Khoury MJ
,
Feero WG ,
Reyes M
,
Citrin T , Freedman A , Leonard D , Burke W ,
Coates R
,
Croyle RT , Edwards K , Kardia S , McBride C , Manolio T , Randhawa G , Rasooly R ,
St Pierre J
,
Terry S .
Genet Med 2009 11 (7) 488-94
The Scientific Foundation for personal genomics: recommendations from a National Institutes of Health-Centers for Disease Control and Prevention multidisciplinary workshop.
Khoury MJ
,
McBride C , Schully SD , Ioannidis JP , Feero WG , Janssens AC ,
Gwinn M
,
Simons-Morton DG ,
Bernhardt JM
,
Cargill M , Chanock SJ , Church GM ,
Coates RJ
,
Collins FS , Croyle RT , Davis BR , Downing GJ , Duross A , Friedman S , Gail MH , Ginsburg GS , Green RC , Greene MH , Greenland P , Gulcher JR , Hsu A , Hudson KL , Kardia SL , Kimmel PL , Lauer MS , Miller AM , Offit K , Ransohoff DF , Roberts HS , Rasooly RS , Stefansson K , Terry SF , Teutsch SM , Trepanier A , Wanke KL , Witte JS , Xu J .
Genet Med 2009 11 (8) 559-67
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Page last reviewed:
Feb 1, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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