Whole exome association of rare deletions in multiplex oral cleft families-Reference-Cited by-全球学者库

Whole exome association of rare deletions in multiplex oral cleft families

Published:2016-12-01 Issue:1 Volume:41 Page:61-69
ISSN:0741-0395
Container-title:Genetic Epidemiology
language:en
Short-container-title:Genet. Epidemiol.

Author:

Fu Jack¹,Beaty Terri H.²,Scott Alan F.³⁴,Hetmanski Jacqueline²,Parker Margaret M.⁵,Wilson Joan E. Bailey⁶,Marazita Mary L.⁷,Mangold Elisabeth⁸,Albacha-Hejazi Hasan⁹,Murray Jeffrey C.¹⁰,Bureau Alexandre¹¹,Carey Jacob²,Cristiano Stephen¹,Ruczinski Ingo¹,Scharpf Robert B.¹²

Affiliation:

1. Department of Biostatistics; Johns Hopkins Bloomberg School of Public Health; Baltimore MD USA

2. Department of Epidemiology; Johns Hopkins Bloomberg School of Public Health; Baltimore MD USA

3. Center for Inherited Disease Research; Johns Hopkins School of Medicine; Baltimore MD USA

4. Institute of Genetic Medicine; Johns Hopkins School of Medicine; Baltimore MD USA

5. Channing Division of Network Medicine; Department of Medicine, Brigham and Women's Hospital; Boston MA USA

6. Inherited Disease Research Branch; National Human Genome Research Institute; National Institutes of Health; Baltimore MD USA

7. Department of Oral Biology; Center for Craniofacial and Dental Genetics; School of Dental Medicine, University of Pittsburgh; PA USA

8. Institute of Human Genetics; University of Bonn; Bonn Germany

9. Dr. Hejazi Clinic; Damascus Syrian Arab Republic

10. Department of Pediatrics; School of Medicine, University of Iowa; IA USA

11. Centre de Recherche de l'Institut Universitaire en Santé Mentale de Québec and Département de Médecine Sociale et Préventive; Université Laval; Québec Canada

12. Department of Oncology; Johns Hopkins School of Medicine; Baltimore MD USA

Funder

National Human Genome Research Institute

National Institutes of Health

Publisher

Wiley

Subject

Genetics(clinical),Epidemiology

Reference39 articles.

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3. A robust statistical method for case-control association testing with copy number variation;Barnes;Nature Genetics,2008