Analysis of sequence data to identify potential risk variants for oral clefts in multiplex families

Author:

Holzinger Emily R.12ORCID,Li Qing1,Parker Margaret M.34,Hetmanski Jacqueline B.5,Marazita Mary L.6,Mangold Elisabeth7,Ludwig Kerstin U.78,Taub Margaret A.9,Begum Ferdouse5,Murray Jeffrey C.10,Albacha-Hejazi Hasan11,Alqosayer Khalid12,Al-Souki Giath13,Albasha Hejazi Abdullatiff14,Scott Alan F.1516,Beaty Terri H.5,Bailey-Wilson Joan E.1

Affiliation:

1. Computational and Statistical Genomics Branch; National Human Genome Research Institute; National Institutes of Health; Baltimore Maryland

2. National Institute of General Medical Sciences; National Institutes of Health; Bethesda Maryland

3. Channing Division of Network Medicine; Brigham and Women's Hospital; Boston Massachusetts

4. Harvard Medical School; Cambridge Massachusetts

5. Department of Epidemiology; Johns Hopkins Bloomberg School of Public Health; Baltimore Maryland

6. Department of Oral Biology; Center for Craniofacial and Dental Genetics; School of Maryland Dental Medicine; University of Pittsburgh; Pittsburgh Pennsylvania

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

8. Department of Genomics; Life & Brain Center; University of Bonn; Bonn Germany

9. Department of Biostatistics; Johns Hopkins Bloomberg School of Public Health; Baltimore Maryland

10. Department of Pediatrics; University of Iowa; Iowa City Iowa

11. Hejazi Clinic; Damascus Syrian Arab Republic

12. Prime Health Clinic; Jeddah Saudi Arabia

13. Saudi Red Crescent; Jeddah Saudi Arabia

14. Al-Eqtisad Est.; Jeddah Saudi Arabia

15. Center for Inherited Disease Research; Johns Hopkins School of Medicine; Baltimore Maryland

16. Institute of Genetic Medicine; Johns Hopkins School of Medicine; Baltimore Maryland

Funder

National Institutes of Health

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

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