Gabrielle J. Halpern

Medicine · Health Sciences

13h-index995citations30works0.02yr avg
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Research Topics

Hemoglobinopathies and Related Disorders(4), Prenatal Screening and Diagnostics(4), Inflammasome and immune disorders(4), Autism Spectrum Disorder Research(3), Genetic and Kidney Cyst Diseases(3)

Publications30 total

Table 1. [Summary of Molecular Genetic Testing Used in Familial Mediterranean Fever].
2014
Familial Mediterranean fever—A review
Genetics in Medicine·2011· 180 citedOpen Access
Prenatal testing and termination of future pregnancies in Arab mothers of children with severe defects: impact of Moslem cleric or physician on the decision making
Open Journal of Genetics·2011· 5 citedOpen Access
Identification of the gene causing long QT syndrome in an Israeli family.
PubMed·2008· 2 cited
Prevalence of breast and colorectal cancer in Ashkenazi Jewish carriers of Fanconi anemia and Bloom syndrome.
PubMed·2007· 30 cited
Genetic screening for autosomal recessive nonsyndromic mental retardation in an isolated population in Israel
European Journal of Human Genetics·2006· 43 citedOpen Access
Consanguinity among the Arab and Jewish populations in Israel.
PubMed·2006· 12 cited
Awareness about problems associated with consanguineous marriages: Survey among Israeli Arab adolescents
Journal of Adolescent Health·2005· 18 cited
A putative new locus for an autosomal recessive cerebellar ataxia syndrome on chromosome 22q11
Clinical Genetics·2005· 3 cited
Knowledge about Consanguineous Marriage Questionnaire
PsycTESTS Dataset·2005
Differences in infant mortality rates between Jews and Arabs in Israel, 1975-2000.
PubMed·2004· 13 cited
Myotonic dystrophy—no evidence for preferential transmission of the mutated allele: A prenatal analysis
American Journal of Medical Genetics Part A·2004· 8 cited
Fragile-X Carrier Screening and the Prevalence of Premutation and Full-Mutation Carriers in Israel
The American Journal of Human Genetics·2001· 228 citedOpen Access
Autosomal dominant nephritis with renal failure of non-Alport type: clinical and molecular studies.
PubMed·2001
Ectodermal dysplasia, ectrodactyly and macular dystrophy (EEM syndrome) in siblings
American Journal of Medical Genetics·2001· 11 cited
Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter
American Journal of Medical Genetics·2001· 14 cited
Trends in the frequencies of consanguineous marriages in the Israeli Arab community
Clinical Genetics·2000· 88 cited
Familial Mediterranean Fever: Effects of Genotype and Ethnicity on Inflammatory Attacks and Amyloidosis
PEDIATRICS·2000· 96 cited
Prenatal diagnosis for detecting congenital malformations: acceptance among Israeli Arab women.
PubMed·2000· 33 cited
Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups
European Journal of Human Genetics·2000· 146 cited
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Frequent Co-authors

Mordechai Shohat(13), Nurit Magal(11), Mordechai Shohat(9), Tamy Shohat(8), Lutfi Jaber(8), Yevgenia Udler(5), Valerie Drasinover(4), Ellen Taub(3), Manfred S. Green(3), Cyril Legum(3), Dov Inbar(3), Carron Sher(3), Miriam Davidovitz(3), Lina Basel‐Vanagaite(2), Bella Davidov(2), Nava Stoffman(2), Yehuda L. Danon(2), Nathan Fischel‐Ghodsian(2), Moshe Fejgin(2), Hagit Baris(2)