Rivka Carmi

Ben-Gurion University of the Negev — Israel

Biochemistry, Genetics and Molecular Biology · Life Sciences

41h-index9.0kcitations151works1.52yr avg
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Research Topics

Genetic and Kidney Cyst Diseases(16), Genetic Syndromes and Imprinting(15), Prenatal Screening and Diagnostics(12), Congenital Anomalies and Fetal Surgery(10), Genetics and Neurodevelopmental Disorders(9)

Publications149 total

When medical duty and advocacy are one-sided, both sides suffer
The Lancet·2024· 1 citedOpen Access
Moral clarity at WHO needs to be clearer
The Lancet·2024· 2 citedOpen Access
WHO's Palestinian statistics: what's Israel got to do with it?
The Lancet·2022
American Funding Cutback to East Jerusalem Hospitals: A Blow to the Health of the City
American Journal of Public Health·2018· 2 citedOpen Access
The Task Force for the Promotion of the Status of Women in Medicine in Israel.
PubMed·2018· 1 cited
Women and health in Israel
The Lancet·2017· 23 cited
The Bardet-Biedl Syndrome
Oxford University Press eBooks·2016· 5 cited
Dedication Ceremony of the Aaron Klug Integrated Centre for Biomolecular Structure and Function
2012
The impact of content-independent mechanisms on guiding attention
Journal of Vision·2010· 2 citedOpen Access
The impact of maturation and aging on mechanisms of attentional selection
Journal of Vision·2010Open Access
From eye-tracking data to information: Lessons from dynamic scenes
Journal of Vision·2010Open Access
Why do we fail to perceive jump-cuts in motion pictures?
Journal of Vision·2010· 1 citedOpen Access
Congenital Glaucoma
Journal of Glaucoma·2010· 13 cited
Quantifying center bias of observers in free viewing of dynamic natural scenes
Journal of Vision·2009· 368 citedOpen Access
A targeted population carrier screening program for severe and frequent genetic diseases in Israel
European Journal of Human Genetics·2008· 65 citedOpen Access
Attitudes toward the acceptability of reasons for pregnancy termination due to fetal abnormalities among prenatal care providers and consumers in Israel
Prenatal Diagnosis·2008· 22 cited
The Bardet–Biedl Syndromes
2008· 3 cited
Deletion of the first pair of fibronectin type III repeats of the integrin β‐4 gene is associated with epidermolysis bullosa, pyloric atresia and aplasia cutis congenita in the original Carmi syndrome patients
American Journal of Medical Genetics Part A·2008· 28 cited
Population history and infrequent mutations: how old is a rare mutation? GUCY2D as a worked example
European Journal of Human Genetics·2007· 12 citedOpen Access
Homozygous<i>CRYBB1</i>Deletion Mutation Underlies Autosomal Recessive Congenital Cataract
Investigative Ophthalmology & Visual Science·2007· 63 cited
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Frequent Co-authors

Val C. Sheffield(22), Edwin M. Stone(14), Khalil Elbedour(12), Daniel Landau(7), Charles Searby(7), Darryl Nishimura(6), Gretel Beck(5), Neena B. Haider(5), Ruth E. Swiderski(5), Samuel G. Jacobson(4), Terry A. Braun(4), Kirk Mykytyn(4), Israel Meizner(4), Hanna Shalev(3), Susan W. Gorman(3), David M. Duhl(3), Richard G. Weleber(3), Thomas L. Casavant(3), Ruti Parvari(3), Joann A. Boughman(3)