Author

H. A. Hamamy

Observed names: H Hamamy, H. HAMAMY, H. Hamamy, H.A. Hamamy

Observed institutions: University of Geneva, University of Jordan, University of Baghdad, Mustansiriyah University, University Hospital of Geneva, National Center for Diabetes, Endocrinology and Genetic Diseases, Jordan University Hospital, University College London

OpenAlex ID: A5110428227

Consanguineous marriages in Jordan: why is the rate changing with time?

2005 · H Hamamy, L Jamhawi, et al. · Clinical Genetics · 144

Community control of genetic and congenital disorders

1997 · Ala Alwan, B. Modell, et al. · Murdoch University Research Portal · 129

Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide

2018 · Congenital Disorders Expert Group, Sowmiya Moorthie, et al. · Journal of Community Genetics · 85

PDF

Genetic Clinics in Arab Communities: Meeting Individual, Family and Community Needs

2008 · H. Hamamy, A.H. Bittles · Public Health Genomics · 53

Hereditary disorders in the Eastern Mediterranean Region.

1994 · H Hamamy, A Alwan · Europe PMC (PubMed Central) · 50

Experience of a multidisciplinary task force with exome sequencing for Mendelian disorders

2016 · S. Fokstuen, P. Makrythanasis, et al. · Human Genomics · 34

PDF

Sanjad Sakati syndrome: a case series from Jordan

2012 · J. Albaramki, K. Akl, et al. · Eastern Mediterranean Health Journal · 30

PDF

Association of Glucose‐6‐Phosphate Dehydrogenase Deficiency with Diabetes Mellitus

1985 · Th. Kh. Saeed, H. A. Hamamy, et al. · Diabetic Medicine · 29

Genetic disorders and congenital abnormalities strategies for reducing the burden in the Region

1997 · H. Hamamy, A. Alwan · Eastern Mediterranean Health Journal · 26

PDF

Prevalence of Consanguineous Marriages in South Sinai, Egypt

2012 · G. YAMAMAH, E. ABDEL-RAOUF, et al. · Journal of Biosocial Science · 24

Precocious puberty at an endocrine centre in Jordan

2004 · B. M. Taher, H. K. Ajlouni, et al. · European Journal of Clinical Investigation · 16

Wrinkly skin syndrome

2005 · H. Hamamy, A. Masri, et al. · Clinical and Experimental Dermatology · 15

Brachydactyly type B1: report of a family with de novo ROR2 mutation

2006 · H Hamamy, N Saleh, et al. · Clinical Genetics · 8

Congenital pseudoarthrosis associated with venous malformation

2006 · A. Al-Hadidy, A. Haroun, et al. · Skeletal Radiology · 6

Sister chromatid exchange frequencies in a group of individuals with unfavorable reproductive health

1992 · H. Hamamy, E.K. Shubber, et al. · European Journal of Obstetrics & Gynecology and Reproductive Biology · 5

PDF

Clinical and inheritance profiles of hyperekplexia in jordan

2007 · A.T. Masri, H.A. Hamamy · Revue Neurologique · 1

Consangunity and psychosis in Algeria. A family study

2015 · A. Dahdouh Guermouche, J. Prados, et al. · European Psychiatry

PDF

412 Combination of Genomic Technologies and Consanguinity in Order to Identify Pathogenic Variants in Recessive Disorders

2012 · P. Makrythanasis, M. Nelis, et al. · Archives of Disease in Childhood

PDF

P97. Loss of CHSY1, a novel FRINGE enzyme, causes syndromic brachydactyly via increased NOTCH signaling

2010 · A.J. Tian, L. Ling, et al. · Differentiation

Mutations in Pycr1 cause progeroid changes in skin and bone due to reduced mitochondrial stress resistance

2010 · B. Reversade, N. Escande-Beillard, et al. · Bone

Works count: 20

Citation count: 655

H-index: 12

I10-index: 12