Stavit A. Shalev

2.1k citations

44 papers · 962 indexed · h-index 19

Co-authors: Joël Zlotogora Judith G. Hall Ohad S. Birk Morad Khayat Zamir Shorer Ortal Barel Rivka Ofir Reiner A. Veitia
Topics: Genomics and Rare Diseases (8 papers)BRCA gene mutations in cancer (5 papers)Genetics and Neurodevelopmental Disorders (5 papers)
Cited by: Genetics Developmental Biology Molecular Biology
Journals: Proceedings of the National Academy of Sciences The American Journal of Human Genetics PLoS Genetics
Partner nations: Israel United States Canada

In The Last Decade

Stavit A. Shalev

42 papers receiving 957 citations

Peers

Countries citing papers authored by Stavit A. Shalev

Since Specialization

Citations

This map shows the geographic impact of Stavit A. Shalev'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 Stavit A. Shalev with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stavit A. Shalev more than expected).

Fields of papers citing papers by Stavit A. Shalev

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stavit A. Shalev. 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 Stavit A. Shalev. The network helps show where Stavit A. Shalev may publish in the future.

Co-authorship network of co-authors of Stavit A. Shalev

This figure shows the co-authorship network connecting the top 25 collaborators of Stavit A. Shalev. A scholar is included among the top collaborators of Stavit A. Shalev 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 Stavit A. Shalev. Stavit A. Shalev 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	Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population 2023 ·Journal of Community Genetics ·(unknown),(unknown),(unknown),(unknown),Morad Khayat,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Ayelet Baram‐Tsabari,Stavit A. Shalev	0
2	The effect of a prior e‐learning tool on genetic counseling outcomes in diverse ethnic couples with abnormal Down syndrome screening tests: A randomized controlled trial 2023 ·Journal of Genetic Counseling ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Morad Khayat,Ayelet Baram‐Tsabari,Stavit A. Shalev	0
3	The landscape of autosomal recessive variants in an isolated community: Implications for population screening for reproductive purposes 2021 ·Clinical Genetics ·Morad Khayat,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Joël Zlotogora,Stavit A. Shalev	2
4	An exome‐wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes 2020 ·Clinical Genetics ·María Isabel Álvarez‐Mora,Anne‐Laure Todeschini,Sandrine Caburet,(unknown),Montserrat Milà,Johnny S. Younis,Stavit A. Shalev,Reiner A. Veitia	13
5	TBCK‐related intellectual disability syndrome: Case study of two patients 2016 ·American Journal of Medical Genetics Part A ·Hanna Mandel,Morad Khayat,(unknown),Orly Elpeleg,Stavit A. Shalev	12
6	Exploring the genetic basis of 3MC syndrome: Findings in 12 further families 2016 ·American Journal of Medical Genetics Part A ·Jill Urquhart,R. C. Roberts,(unknown),Stavit A. Shalev,(unknown),Sheela Nampoothiri,Yves Sznajer,Nicole Revençu,(unknown),Mohnish Suri,Jamie M. Ellingford,Simon G. Williams,Sanjeev S. Bhaskar,Jill Clayton‐Smith	22
7	Novel Homozygous Missense Mutation in SPG20 Gene Results in Troyer Syndrome Associated with Mitochondrial Cytochrome c Oxidase Deficiency 2016 ·JIMD Reports ·Ronen Spiegel,Devorah Soiferman,Avraham Shaag,Stavit A. Shalev,Orly Elpeleg,Ann Saada	15
8	Novel mutation in TSPAN12 leads to autosomal recessive inheritance of congenital vitreoretinal disease with intra‐familial phenotypic variability 2014 ·American Journal of Medical Genetics Part A ·Moran Gal,Erez Y. Levanon,(unknown),Morad Khayat,Jacob Pe’er,Stavit A. Shalev	19
9	Marriage Patterns and Reproductive Decision-Making in the Inhabitants of a Single Muslim Village during a 50-Year Period 2014 ·Human Heredity ·Joël Zlotogora,Stavit A. Shalev	6
10	Oculopharyngeal muscular dystrophy among Bulgarian Jews: a new cluster? 2013 ·PubMed ·Sergiu C. Blumen,Anat Kesler,Ron Dabby,Stavit A. Shalev,Morad Khayat,(unknown),J Zoldan,Felix Benninger,Vivian E. Drory,Michael Gurevich,Menachem Sadeh,Bernard Brais,Itzhak Braverman	7
11	Acrocallosal syndrome: Identification of a novel KIF7 mutation and evidence for oligogenic inheritance 2012 ·European Journal of Medical Genetics ·(unknown),Stavit A. Shalev,Michael A. Simpson,Neil V. Morgan,(unknown),Juan Chemke,Richard C. Trembath,Eamonn R. Maher	21
12	Clinical characterization of a newly described neonatal diabetes syndrome caused by RFX6 mutations 2011 ·American Journal of Medical Genetics Part A ·Ronen Spiegel,Angus Dobbie,Corina Hartman,Liat de Vries,Sian Ellard,Stavit A. Shalev	33
13	Intracerebral large artery disease in Aicardi–Goutières syndrome implicates SAMHD1 in vascular homeostasis 2010 ·Developmental Medicine & Child Neurology ·Venkateswaran Ramesh,Bruno De Bernardi,(unknown),Caterina Garone,Emilio Franzonı,Mario Abinun,Patrick Mitchell,Dipayan Mitra,Mark Friswell,John W. Nelson,Stavit A. Shalev,Gillian Rice,Hannah Gornall,Marcin Szynkiewicz,(unknown),Vijeya Ganesan,Julie Prendiville,John H. Livingston,Yanick J. Crow	73
14	Further delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3 2010 ·European Journal of Human Genetics ·Siddharth Banka,(unknown),William G. Newman,Yanick J. Crow,(unknown),Joanne Yacobovich,Dian Donnai,Stavit A. Shalev	36
15	Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9 2008 ·The American Journal of Human Genetics ·Ortal Barel,Stavit A. Shalev,Rivka Ofir,Asi Cohen,Joël Zlotogora,Zamir Shorer,(unknown),Gal Finer,(unknown),Noam Zilberberg,Ohad S. Birk	137
16	A syndrome characterized by intra‐uterine lower limb dislocation, gracile bones, clubfeet, and other skeletal features 2007 ·American Journal of Medical Genetics Part A ·Stavit A. Shalev	2
17	Population history and infrequent mutations: how old is a rare mutation? GUCY2D as a worked example 2007 ·European Journal of Human Genetics ·Sylvain Hanein,Isabelle Perrault,S. Gerber,Nathalie Delphin,David BenEzra,Stavit A. Shalev,Rivka Carmi,Josué Feingold,Jean‐Louis Dufier,Arnold Münnich,Josseline Kaplan,Jean‐Michel Rozet,Marc Jeanpierre	5
18	A syndrome characterized by contractures and pterygia of upper body associated with umbilical hernia, short stature, and distinctive face in an Arabic family 2005 ·American Journal of Medical Genetics Part A ·Stavit A. Shalev,Ronen Spiegel,Judith G. Hall	3
19	Long‐term follow‐up of three individuals with Kabuki syndrome 2003 ·American Journal of Medical Genetics Part A ·Stavit A. Shalev,L. Clarke,(unknown),Sylvie Langlois,Elaine H. Zackai,Judith G. Hall,Donna M. McDonald‐McGinn	17
20	Poland anomaly—report of an unusual family 2002 ·American Journal of Medical Genetics Part A ·Stavit A. Shalev,Judith G. Hall	21

About Stavit A. Shalev

Stavit A. Shalev is a scholar working on Genetics, Developmental Biology and Pediatrics, Perinatology and Child Health, having authored 44 papers that have together received 962 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (8 papers), BRCA gene mutations in cancer (5 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Genetics (416 citations), Developmental Biology (21 citations) and Molecular Biology (519 citations). Stavit A. Shalev has collaborated with scholars based in Israel, United States and Canada. Frequent co-authors include Joël Zlotogora, Judith G. Hall, Ohad S. Birk, Morad Khayat, Zamir Shorer, Ortal Barel, Rivka Ofir, Reiner A. Veitia, Asi Cohen and Sandrine Caburet. Their work appears in journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and PLoS Genetics.

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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