Stavit A. Shalev

2.1k citations

44 papers · 962 indexed · h-index 19

Genetics top 5%
- Genomics and Rare Diseases 8
- BRCA gene mutations in cancer 5
- Genetics and Neurodevelopmental Disorders 5
- Genetic Syndromes and Imprinting 3
Developmental Biology top 10%
Molecular Biology
- Hedgehog Signaling Pathway Studies 3
Cell Biology
Reproductive Medicine top 10%
Pathology and Forensic Medicine
- Genetic factors in colorectal cancer 3
Pediatrics, Perinatology and Child Health
- Prenatal Screening and Diagnostics 3
Neurology
- Neurological diseases and metabolism 2

Co-authors: Joël Zlotogora Judith G. Hall Ohad S. Birk Morad Khayat Zamir Shorer Ortal Barel Rivka Ofir Reiner A. Veitia
Cited by: Genetics Developmental Biology Molecular Biology
Journals: Proceedings of the National Academy of Sciences (1 paper)The American Journal of Human Genetics (2 papers)PLoS Genetics (1 paper)
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

The 25 scholars most cited alongside Stavit A. Shalev, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Stavit A. Shalev Line = papers co-authored together Stavit A. Shalev links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Educational tools support informed decision-making for genetic carrier screening in a heterogenic Israeli population Journal of Community Genetics ·Chen Gafni‐Amsalem,Olfat Aboleil‐Zoubi,Elena Chervinsky,Ola Aleme,Morad Khayat,Husam Bashir,Lilach Peled Perets,Efrat Mamluk,Shadia Hakrosh,Shoshi Kurtzman,Liron Tamir,Ayelet Baram‐Tsabari,Stavit A. Shalev	2023	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 Journal of Genetic Counseling ·Olfat Aboleil‐Zoubi,Chen Gafni‐Amsalem,Lilach Peled‐Perets,Efrat Mamluk,Liron Tamir,Shadia Hakrosh,Shoshana Kurtzman,Elena Chervinsky,Ula Aalimi,Bashir Husam,Morad Khayat,Ayelet Baram‐Tsabari,Stavit A. Shalev	2023	0
3	The landscape of autosomal recessive variants in an isolated community: Implications for population screening for reproductive purposes Clinical Genetics ·Morad Khayat,Nada Danial‐Farran,Elena Chervinsky,Yoav Zehavi,Lilach Peled‐Peretz,Chen Gafni‐Amsalem,Shadia Hakrosh,Olfat Abu‐Leil Zouabi,Liron Tamir,Efrat Mamlouk,Joël Zlotogora,Stavit A. Shalev	2021	2
4	An exome‐wide exploration of cases of primary ovarian insufficiency uncovers novel sequence variants and candidate genes Clinical Genetics ·María Isabel Álvarez‐Mora,Anne‐Laure Todeschini,Sandrine Caburet,Lilach Peled Perets,Montserrat Milà,Johnny S. Younis,Stavit A. Shalev,Reiner A. Veitia	2020	13
5	TBCK‐related intellectual disability syndrome: Case study of two patients American Journal of Medical Genetics Part A ·Hanna Mandel,Morad Khayat,Elana Chervinsky,Orly Elpeleg,Stavit A. Shalev	2016	12
6	Exploring the genetic basis of 3MC syndrome: Findings in 12 further families American Journal of Medical Genetics Part A ·Jill Urquhart,R. C. Roberts,Deepthi De Silva,Stavit A. Shalev,Elena Chervinsky,Sheela Nampoothiri,Yves Sznajer,Nicole Revençu,Romesh Gunasekera,Mohnish Suri,Jamie M. Ellingford,Simon G. Williams,Sanjeev S. Bhaskar,Jill Clayton‐Smith	2016	22
7	Novel Homozygous Missense Mutation in SPG20 Gene Results in Troyer Syndrome Associated with Mitochondrial Cytochrome c Oxidase Deficiency JIMD Reports ·Ronen Spiegel,Devorah Soiferman,Avraham Shaag,Stavit A. Shalev,Orly Elpeleg,Ann Saada	2016	15
8	Novel mutation in TSPAN12 leads to autosomal recessive inheritance of congenital vitreoretinal disease with intra‐familial phenotypic variability American Journal of Medical Genetics Part A ·Moran Gal,Erez Y. Levanon,Yasir Hujeirat,Morad Khayat,Jacob Pe’er,Stavit A. Shalev	2014	19
9	Marriage Patterns and Reproductive Decision-Making in the Inhabitants of a Single Muslim Village during a 50-Year Period Human Heredity ·Joël Zlotogora,Stavit A. Shalev	2014	6
10	Oculopharyngeal muscular dystrophy among Bulgarian Jews: a new cluster? PubMed ·Sergiu C. Blumen,Anat Kesler,Ron Dabby,Stavit A. Shalev,Morad Khayat,Yechoshua Almog,J Zoldan,Felix Benninger,Vivian E. Drory,Michael Gurevich,Menachem Sadeh,Bernard Brais,Itzhak Braverman	2013	7
11	Acrocallosal syndrome: Identification of a novel KIF7 mutation and evidence for oligogenic inheritance European Journal of Medical Genetics ·Diana Walsh,Stavit A. Shalev,Michael A. Simpson,Neil V. Morgan,Zulema Gelman-Kohan,Juan Chemke,Richard C. Trembath,Eamonn R. Maher	2012	21
12	Clinical characterization of a newly described neonatal diabetes syndrome caused by RFX6 mutations American Journal of Medical Genetics Part A ·Ronen Spiegel,Angus Dobbie,Corina Hartman,Liat de Vries,Sian Ellard,Stavit A. Shalev	2011	33
13	Intracerebral large artery disease in Aicardi–Goutières syndrome implicates SAMHD1 in vascular homeostasis Developmental Medicine & Child Neurology ·Venkateswaran Ramesh,Bruno De Bernardi,A. Stafa,Caterina Garone,Emilio Franzonı,Mario Abinun,Patrick Mitchell,Dipayan Mitra,Mark Friswell,John W. Nelson,Stavit A. Shalev,Gillian Rice,Hannah Gornall,Marcin Szynkiewicz,FRANÇOIS AYMARD,Vijeya Ganesan,Julie Prendiville,John H. Livingston,Yanick J. Crow	2010	73
14	Further delineation of the phenotype of severe congenital neutropenia type 4 due to mutations in G6PC3 European Journal of Human Genetics ·Siddharth Banka,Elena Chervinsky,William G. Newman,Yanick J. Crow,Shay Yeganeh,Joanne Yacobovich,Dian Donnai,Stavit A. Shalev	2010	36
15	Maternally Inherited Birk Barel Mental Retardation Dysmorphism Syndrome Caused by a Mutation in the Genomically Imprinted Potassium Channel KCNK9 The American Journal of Human Genetics ·Ortal Barel,Stavit A. Shalev,Rivka Ofir,Asi Cohen,Joël Zlotogora,Zamir Shorer,Galia Mazor,Gal Finer,Shareef Khateeb,Noam Zilberberg,Ohad S. Birk	2008	137
16	A syndrome characterized by intra‐uterine lower limb dislocation, gracile bones, clubfeet, and other skeletal features American Journal of Medical Genetics Part A ·Stavit A. Shalev	2007	2
17	Population history and infrequent mutations: how old is a rare mutation? GUCY2D as a worked example 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	2007	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 American Journal of Medical Genetics Part A ·Stavit A. Shalev,Ronen Spiegel,Judith G. Hall	2005	3
19	Long‐term follow‐up of three individuals with Kabuki syndrome American Journal of Medical Genetics Part A ·Stavit A. Shalev,L. Clarke,David Koehn,Sylvie Langlois,Elaine H. Zackai,Judith G. Hall,Donna M. McDonald‐McGinn	2003	17
20	Poland anomaly—report of an unusual family American Journal of Medical Genetics Part A ·Stavit A. Shalev,Judith G. Hall	2002	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), Genetics and Neurodevelopmental Disorders (5 papers), Genetic Syndromes and Imprinting (3 papers), Hedgehog Signaling Pathway Studies (3 papers), Genetic factors in colorectal cancer (3 papers), Prenatal Screening and Diagnostics (3 papers) and Neurological diseases and metabolism (2 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.

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