Rivka Carmi - Publications, H-index & Citations

WHO's Palestinian statistics: what's Israel got to do with it?

IF88.5

2024-03-01

OAAI

Beyar, Rafael; Blazer, Shraga; Breuer, Edward; Carmi, Rivka; Ciechanover, Aaron; Clarfield, A. Mark; Glick, Shimon; Magen, Daniella; Manor, Orly; Paltiel, Ora; Skorecki, Karl

American Funding Cutback to East Jerusalem Hospitals: A Blow to the Health of the City

IF88.5

2022-08-01

PREAI

Skorecki, Karl; Beyar, Rafi; Carmi, Rivka; Clarfield, A. Mark; Glick, Shimon; Manor, Orly; Reis, Shmuel

AMERICAN JOURNAL OF PUBLIC HEALTH

IF9.6

2018-12-01

OAAI

Clarfield, A. Mark; Skorecki, Karl; Paltiel, Ora; Glick, Shimon M.; Beyar, Rafi; Ben Yehuda, Dina; Carmi, Rivka; Gil, Ziv; Billan, Salem; Azzam, Zaher; Basis, Fuad; Levy-Lahad, Ephrat; Lahad, Amnon; Izraeli, Shai; Turner, Dan; Halevy, Yonatan

Women and health in Israel

A targeted population carrier screening program for severe and frequent genetic diseases in Israel

IF88.5

2017-06-01

PREAI

Granek, Leeat; Nakash, Ora; Carmi, Rivka

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2008-12-24

OAAI

Zlotogora, Joel; Carmi, Rivka; Lev, Boaz; Shalev, Stavit A.

Population history and infrequent mutations:: how old is a rare mutation?: GUCY2D as a worked example

EUROPEAN JOURNAL OF HUMAN GENETICS

IF4.6

2007-08-08

OAAI

Hanein, Sylvain; Perrault, Isabelle; Gerber, Sylvie; Delphin, Nathalie; Benezra, David; Shalev, Stavit; Carmi, Rivka; Feingold, Josue; Dufier, Jean-Louis; Munnich, Arnold; Kaplan, Josseline; Rozet, Jean-Michel; Jeanpierre, Marc

Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract

INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE

IF4.7

2007-05-01

PREAI

Cohen, David; Bar-Yosef, Udy; Levy, Jaime; Gradstein, Libe; Belfair, Nadav; Ofir, Rivka; Joshua, Sarah; Lifshitz, Tova; Carmi, Rivka; Birk, Ohad S.

Homozygosity mapping with SNP arrays identifies TRIM32 an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2006-04-18

414

OAAI

Chiang, AP; Beck, JS; Yen, HJ; Tayeh, MK; Scheetz, TE; Swiderski, RE; Nishimura, DY; Braun, TA; Kim, KYA; Huang, J; Elbedour, K; Carmi, R; Slusarski, DC; Casavant, TL; Stone, EM; Sheffield, VC

Promoting Arab and Israeli cooperation: peacebuilding through health initiatives 促进阿拉伯和以色列的合作: 通过卫生倡议建设和平

Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin

IF88.5

2005-04-01

PREAI

Skinner, H; Abdeen, Z; Abdeen, H; Aber, P; Al-Masri, M; Attias, J; Avraham, KB; Carmi, R; Chalin, C; El Nasser, Z; Hijazi, M; Jebara, RO; Kanaan, M; Pratt, H; Raad, F; Roth, Y; Williams, AP; Noyek, A

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2004-11-11

363

OAAI

Nishimura, DY; Fath, M; Mullins, RF; Searby, C; Andrews, M; Davis, R; Andorf, JL; Mykytyn, K; Swiderski, RE; Yang, BL; Carmi, R; Stone, EM; Sheffield, VC

Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)

Evaluation of complex inheritance involving the most common Bardet-Biedl syndrome locus (BBS1)

IF8.1

2004-09-01

212

OAAI

Chiang, AP; Nishimura, D; Searby, C; Elbedour, K; Carmi, R; Ferguson, AL; Secrist, J; Braun, T; Casavant, T; Stone, EM; Sheffield, VC

Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndrome

IF8.1

2003-02-01

105

OAAI

Mykytyn, K; Nishimura, DY; Searby, CC; Beck, G; Bugge, K; Haines, HL; Cornier, AS; Cox, GF; Fulton, AB; Carmi, R; Iannaccone, A; Jacobson, SG; Weleber, RG; Wright, AF; Riise, R; Hennekam, RCM; Lüleci, G; Berker-Karauzum, S; Biesecker, LG; Stone, EM; Sheffield, VC

HLA DQA1-DQB1 genotypes in Bedouin families with celiac disease

IF31.8

2002-07-15

299

PREAI

Mykytyn, K; Nishimura, DY; Searby, CC; Shastri, M; Yen, HJ; Beck, JS; Braun, T; Streb, LM; Cornier, AS; Cox, GF; Fulton, AB; Carmi, R; Lüleci, G; Chandrasekharappa, SC; Collins, FS; Jacobson, SG; Heckenlively, JR; Weleber, RG; Stone, EM; Sheffield, VC

HUMAN IMMUNOLOGY

IF2.2

2002-06-01

PREAI

Neuhausen, SL; Weizman, Z; Camp, NJ; Elbedour, K; Sheffield, VC; Zone, JJ; Carmi, R

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C

IF31.8

2002-05-28

463

PREAI

Walder, RY; Landau, D; Meyer, P; Shalev, H; Tsolia, M; Borochowitz, Z; Boettger, MB; Beck, GE; Englehardt, RK; Carmi, R; Sheffield, VC

GENETICS IN MEDICINE

IF6.2

2001-09-01

OAAI

Meiner, V; Shpitzen, S; Mandel, H; Klar, A; Ben-Neriah, Z; Zlotogora, J; Sagi, M; Lossos, A; Bargal, R; Sury, V; Carmi, R; Leitersdorf, E; Zeigler, M

Identification of the gene that, when mutated, causes the human obesity syndrome BBS4

Complement factor h gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome - Reply to Buddles et al.

IF31.8

2001-06-01

243

PREAI

Mykytyn, K; Braun, T; Carmi, R; Haider, NB; Searby, CC; Shastri, M; Beck, G; Wright, AF; Iannaccone, A; Elbedour, K; Riise, R; Baldi, A; Raas-Rothschild, A; Gorman, SW; Duhl, DM; Jacobson, SG; Casavant, T; Stone, EM; Sheffield, VC

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate

IF8.1

2000-05-01

OAAI

Sheffield, VC; Ying, LH; Carmi, R; Landau, D

Complement factor H gene mutation associated with autosomal recessive atypical hemolytic uremic syndrome

IF31.8

2000-02-01

419

PREAI

Haider, NB; Jacobson, SG; Cideciyan, AV; Swiderski, R; Streb, LM; Searby, C; Beck, G; Hockey, R; Hanna, DB; Gorman, S; Duhl, D; Carmi, R; Bennett, J; Weleber, RG; Fishman, GA; Wright, AF; Stone, EM; Sheffield, VC