Ziva Ben‐Neriah

2.4k total citations
40 papers, 1.4k citations indexed

About

Ziva Ben‐Neriah is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Ziva Ben‐Neriah has authored 40 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 16 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Ziva Ben‐Neriah's work include Prenatal Screening and Diagnostics (7 papers), Genetic Syndromes and Imprinting (6 papers) and Metabolism and Genetic Disorders (5 papers). Ziva Ben‐Neriah is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genetic Syndromes and Imprinting (6 papers) and Metabolism and Genetic Disorders (5 papers). Ziva Ben‐Neriah collaborates with scholars based in Israel, United States and France. Ziva Ben‐Neriah's co-authors include Israela Lerer, Dvorah Abeliovich, Michal Sagi, Annick Raas‐Rothschild, Haya Levi, David Zangen, Judith Melki, Reiner A. Veitia, Daniel Vaiman and Sandrine Caburet and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Ziva Ben‐Neriah

39 papers receiving 1.4k citations

Peers

Countries citing papers authored by Ziva Ben‐Neriah

Since Specialization

Citations

This map shows the geographic impact of Ziva Ben‐Neriah's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ziva Ben‐Neriah with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ziva Ben‐Neriah more than expected).

Fields of papers citing papers by Ziva Ben‐Neriah

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ziva Ben‐Neriah. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ziva Ben‐Neriah. The network helps show where Ziva Ben‐Neriah may publish in the future.

Co-authorship network of co-authors of Ziva Ben‐Neriah

This figure shows the co-authorship network connecting the top 25 collaborators of Ziva Ben‐Neriah. A scholar is included among the top collaborators of Ziva Ben‐Neriah based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ziva Ben‐Neriah. Ziva Ben‐Neriah is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Mutant Cohesin in Premature Ovarian Failure 2014 ·New England Journal of Medicine ·Sandrine Caburet, Valerie A. Arboleda, Elena Llano, Paul A. Overbeek, José Luís Barbero, Kazuhiro Oka, Wilbur R. Harrison, Daniel Vaiman, Ziva Ben‐Neriah, Ignacio García‐Tuñón, Marc Fellous, Alberto M. Pendás, Reiner A. Veitia, Éric Vilain	196
2	Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure 2012 ·LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) ·Sandrine Caburet, Petra Zavadáková, Ziva Ben‐Neriah, (unknown), Paul Laissue, Vered Chalifa‐Caspi, Daniel Vaiman, Giovanni Levi, Reiner A. Veitia, Marc Fellous	0
3	Genome-Wide Linkage in a Highly Consanguineous Pedigree Reveals Two Novel Loci on Chromosome 7 for Non-Syndromic Familial Premature Ovarian Failure 2012 ·PLoS ONE ·Sandrine Caburet, Petra Zavadáková, Ziva Ben‐Neriah, (unknown), Aurélie Dipietromaria, Céline Charon, Céline Besse, Paul Laissue, Vered Chalifa‐Caspi, Sophie Christin‐Maître, Daniel Vaiman, Giovanni Levi, Reiner A. Veitia, Marc Fellous	27
4	Novel mutations of MYO7A and USH1G in Israeli Arab families with Usher syndrome type 1. 2011 ·PubMed Central ·(unknown), (unknown), Stavit Shalev, Eedy Mezer, (unknown), Ziva Ben‐Neriah, (unknown), Daniel Briscoe, Tamar Ben‐Yosef	9
5	Genomic Duplication and Overexpression of TJP2/ZO-2 Leads to Altered Expression of Apoptosis Genes in Progressive Nonsyndromic Hearing Loss DFNA51 2010 ·The American Journal of Human Genetics ·Tom Walsh, Sarah B. Pierce, Danielle R. Lenz, Zippora Brownstein, Orit Dagan‐Rosenfeld, Hashem Shahin, Wendy Roeb, Shane McCarthy, Alex S. Nord, Carlos R. Gordon, Ziva Ben‐Neriah, Jonathan Sebat, Moien Kanaan, Ming K. Lee, Moshe Frydman, Mary‐Claire King, Karen B. Avraham	74
6	Mutation of SYNE-1, encoding an essential component of the nuclear lamina, is responsible for autosomal recessive arthrogryposis 2009 ·Human Molecular Genetics ·(unknown), Nasim Warwar, Alain Israël, Irina Gurt, Elizabeth M. McNally, Megan J. Puckelwartz, Benjamin S. Glick, Yuval Nevo, Ziva Ben‐Neriah, Judith Melki	108
7	Mutations in DDR2 Gene Cause SMED with Short Limbs and Abnormal Calcifications 2008 ·The American Journal of Human Genetics ·Ruth Bargal, Valérie Cormier‐Daire, Ziva Ben‐Neriah, Martine Le Merrer, Jacob Sosna, Judith Melki, David Zangen, Sarah Smithson, Zvi Borochowitz, Ruth Belostotsky, Annick Raas‐Rothschild	82
8	Misleading findings of homozygosity mapping resulting from three novel mutations in NPHS1 encoding nephrin in a highly inbred community 2007 ·Genetics in Medicine ·Yaacov Frishberg, Ziva Ben‐Neriah, (unknown), Choni Rinat, Minna Männikkö, Sofia Feinstein, Rachel Becker‐Cohen, Hannu Jalanko, Joël Zlotogora, Marjo Kestilä	14
9	Glutaric aciduria type 1: Clinical, biochemical and molecular findings in patients from Israel 2007 ·European Journal of Paediatric Neurology ·Stanley H. Korman, Cornelis Jakobs, (unknown), Alisa Gutman, Marjo S. van der Knaap, Ziva Ben‐Neriah, (unknown), Isaiah D. Wexler, Gajja S. Salomons	31
10	Impaired Mitochondrial Glutamate Transport in Autosomal Recessive Neonatal Myoclonic Epilepsy 2005 ·The American Journal of Human Genetics ·Florence Molinari, Annick Raas‐Rothschild, Marlène Rio, Giuseppe Fiermonte, Férechté Encha‐Razavi, Luigi Palmieri, Ferdinando Palmieri, Ziva Ben‐Neriah, Noman Kadhom, Michel Vekemans, Tania Attié‐Bitach, Arnold Münnich, Pierre Rustin, Laurence Colleaux	115
11	A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem 2005 ·Journal of Human Genetics ·Avihu Boneh, Stanley H. Korman, Ken‐ichi Sato, Junko Kanno, Yoichi Matsubara, Israela Lerer, Ziva Ben‐Neriah, Shigeo Kure	19
12	Chromosome aberration and environmental physical activity: Down syndrome and solar and cosmic ray activity, Israel, 1990–2000 2005 ·International Journal of Biometeorology ·E Stoupel, (unknown), Z. Appelman, Ziva Ben‐Neriah, Hanna Dar, Moshe Fejgin, Ruth Gershoni‐Baruch, Esther Manor, Gad Barkai, Stavit Shalev, Z Gelman-Kohan, Orit Reish, Dorit Lev, Bella Davidov, Boleslaw Goldman, Mordechai Shohat	20
13	Prenatal diagnosis for arginase deficiency by second‐trimester fetal erythrocyte arginase assay and first‐trimester ARG1 mutation analysis 2004 ·Prenatal Diagnosis ·Stanley H. Korman, Alisa Gutman, (unknown), (unknown), Ziva Ben‐Neriah, Marsha Zeigler	9
14	Prenatal diagnosis of Down syndrome: Ten year experience in the Israeli population 2003 ·American Journal of Medical Genetics Part A ·Mordechai Shohat, (unknown), (unknown), (unknown), Z. Appelman, Ziva Ben‐Neriah, Hanna Dar, Avi Orr‐Urtreger, Aliza Amiel, Ruth Gershoni, Esther Manor, Gad Barkai, Stavit Shalev, (unknown), Orit Reish, Dorit Lev, Bella Davidov, Boleslaw Goldman	24
15	Clinical-biochemical correlation in molecularly characterized patients with Niemann-Pick type C 2001 ·Genetics in Medicine ·Vardiella Meiner, Shoshi Shpitzen, Hanna Mandel, Aharon Klar, Ziva Ben‐Neriah, Joël Zlotogora, Michal Sagi, (unknown), Ruth Bargal, (unknown), Rivka Carmi, Eran Leitersdorf, Marsha Zeigler	28
16	A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews 2001 ·Human Mutation ·Israela Lerer, Michal Sagi, Ziva Ben‐Neriah, (unknown), Haya Levi, Dvorah Abeliovich	173
17	Renal anomalies in Marden‐Walker syndrome: A clue for prenatal diagnosis 1995 ·American Journal of Medical Genetics ·Ziva Ben‐Neriah, Simcha Yagel, Ilana Ariel	4
18	Amniocentesis rate and the detection of down syndrome and other chromosomal anomalies in Israel 1995 ·Prenatal Diagnosis ·Mordechai Shohat, (unknown), Bella Davidov, Gad Barkai, Cyril Legum, M David, Hanna Dar, Yitzhak Romem, Aliza Amiel, (unknown), Gideon Bach, Ziva Ben‐Neriah, Ruth Sheffer, Z. Appelman, Juan Chemke, (unknown), (unknown), Boleslaw Goldman	12
19	Physiology: The regulatory role of tri-iodothyronine on the production of α-fetoprotein and albumin by mouse fetal liver cells* 1993 ·Human Reproduction ·Eyal Y. Anteby, (unknown), Matat Dushnik, (unknown), (unknown), Ziva Ben‐Neriah, Simcha Yagel	8
20	Survival in an Infant with a Prenatally Diagnosed Meckel Syndrome Variant 1993 ·American Journal of Perinatology ·Michael Kaplan, Ziva Ben‐Neriah, (unknown)	3

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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