Ginat Narkis

1.2k total citations
23 papers, 836 citations indexed

About

Ginat Narkis is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Ginat Narkis has authored 23 papers receiving a total of 836 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Cell Biology. Recurrent topics in Ginat Narkis's work include Neurogenetic and Muscular Disorders Research (4 papers), Biochemical and Molecular Research (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Ginat Narkis is often cited by papers focused on Neurogenetic and Muscular Disorders Research (4 papers), Biochemical and Molecular Research (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). Ginat Narkis collaborates with scholars based in Israel, United States and Singapore. Ginat Narkis's co-authors include Ohad S. Birk, Rivka Ofir, Khalil Elbedour, Daniella Landau, Hagit Flusser, Zamir Shorer, Esther Manor, Aharon Galil, Ilan Shelef and Rachel Lévy and has published in prestigious journals such as Development, Annals of Neurology and The American Journal of Human Genetics.

In The Last Decade

Ginat Narkis

21 papers receiving 823 citations

Peers

Ginat Narkis

NEURO

GENET

Lorena Travaglini Italy

Chandree L. Beaulieu Canada

Pengfei Lin China

Anna Ardissone Italy

Annabelle Chaussenot France

Laura Cassina Italy

Lori M. Roberts United States

Ruth Sheffer Israel

Laura Davis Keppen United States

Laura Napoli Italy

Lorena Travaglini Italy

Ginat Narkis

1.2k ×2.2

68 ×0.5

NEURO

299 ×2.4

GENET

115 ×1.1

67 ×0.7

Citations per year, relative to Ginat Narkis Ginat Narkis (= 1×) peers Lorena Travaglini

Countries citing papers authored by Ginat Narkis

Since Specialization

Citations

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

Fields of papers citing papers by Ginat Narkis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ginat Narkis. 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 Ginat Narkis. The network helps show where Ginat Narkis may publish in the future.

Co-authorship network of co-authors of Ginat Narkis

This figure shows the co-authorship network connecting the top 25 collaborators of Ginat Narkis. A scholar is included among the top collaborators of Ginat Narkis 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 Ginat Narkis. Ginat Narkis is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Chabosseau, Pauline, Iris Noyman, Orna Staretz‐Chacham, et al.. (2025). Severe neonatal hypotonia due to SLC30A5 variant affecting function of ZnT5 zinc transporter. JIMD Reports. 66(1). e12465–e12465.

Yogev, Yuval, Ohad Wormser, Daniel Halpérin, et al.. (2024). VARista: a free web platform for streamlined whole-genome variant analysis across T2T, hg38, and hg19. Human Genetics. 143(5). 695–701. 5 indexed citations

Levy, Michal, Mordechai Shohat, Sarit Kahana, et al.. (2024). Exploring inheritance, and clinical penetrance of distal Xq28 duplication syndrome: insights from 47 new unpublished cases. Journal of Human Genetics. 69(7). 337–343.

Gradstein, Libe, Yuri V. Sergeev, Itay Lavy, et al.. (2016). Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred. BMC Medical Genetics. 17(1). 52–52. 13 indexed citations

David, Ahuvit, Yotam Menuchin-Lasowski, Ginat Narkis, et al.. (2016). The stage-dependent roles of Ldb1 and functional redundancy with Ldb2 in mammalian retinogenesis. Development. 143(22). 4182–4192. 23 indexed citations

Flusser, Hagit, Barak Markus, Zamir Shorer, et al.. (2014). A syndrome of congenital microcephaly, intellectual disability and dysmorphism with a homozygous mutation in FRMD4A. European Journal of Human Genetics. 23(12). 1729–1734. 13 indexed citations

Cohen, Idan, Eldad Silberstein, Yonatan Perez, et al.. (2013). Autosomal recessive Adams–Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase. European Journal of Human Genetics. 22(3). 374–378. 45 indexed citations

Narkis, Ginat, et al.. (2012). Isl1 and Ldb Co‐regulators of transcription are essential early determinants of mouse limb development. Developmental Dynamics. 241(4). 787–791. 28 indexed citations

Markus, Barak, Ginat Narkis, Daniella Landau, et al.. (2012). Autosomal recessive lethal congenital contractural syndrome type 4 (LCCS4) caused by a mutation in MYBPC1. Human Mutation. 33(10). 1435–1438. 45 indexed citations

10.

Gradstein, Libe, Annika Pasanen, Rivka Ofir, et al.. (2011). High Myopia Caused by a Mutation in LEPREL1, Encoding Prolyl 3-Hydroxylase 2. The American Journal of Human Genetics. 89(3). 438–445. 81 indexed citations

11.

Zeev, Bruria Ben, Dorit Lev, Dan Su, et al.. (2010). Mutations Disrupting Selenocysteine Formation Cause Progressive Cerebello-Cerebral Atrophy. The American Journal of Human Genetics. 87(4). 538–544. 107 indexed citations

12.

Barel, Ortal, Zamir Shorer, Hagit Flusser, et al.. (2008). Mitochondrial Complex III Deficiency Associated with a Homozygous Mutation in UQCRQ. The American Journal of Human Genetics. 82(5). 1211–1216. 92 indexed citations

13.

Narkis, Ginat, Rivka Ofir, Esther Manor, et al.. (2007). Lethal Congenital Contractural Syndrome Type 2 (LCCS2) Is Caused by a Mutation in ERBB3 (Her3), a Modulator of the Phosphatidylinositol-3-Kinase/Akt Pathway. The American Journal of Human Genetics. 81(3). 589–595. 49 indexed citations

14.

Narkis, Ginat, Rivka Ofir, Daniella Landau, et al.. (2007). Lethal Contractural Syndrome Type 3 (LCCS3) Is Caused by a Mutation in PIP5K1C, Which Encodes PIPKIγ of the Phophatidylinsitol Pathway. The American Journal of Human Genetics. 81(3). 530–539. 79 indexed citations

15.

Flusser, Hagit, Rivka Ofir, Ilan Shelef, et al.. (2006). PLA2G6 Mutation Underlies Infantile Neuroaxonal Dystrophy. The American Journal of Human Genetics. 79(5). 942–948. 145 indexed citations

16.

Narkis, Ginat, Daniella Landau, Esther Manor, Rivka Ofir, & Ohad S. Birk. (2006). Genetics of Arthrogryposis. Clinical Orthopaedics and Related Research. 456. 30–35. 11 indexed citations

17.

Narkis, Ginat, Daniella Landau, Esther Manor, et al.. (2004). Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13. American Journal of Medical Genetics Part A. 130A(3). 272–276. 15 indexed citations

18.

Hershkovitz, Eli, Ginat Narkis, Zamir Shorer, et al.. (2002). Cerebral X‐linked adrenoleukodystrophy in a girl with Xq27‐Ter deletion. Annals of Neurology. 52(2). 234–237. 19 indexed citations

19.

Parvari, Ruti, Ke-Jian Lei, László Szönyi, et al.. (1998). Two new mutations in the glucose-6-phosphatase gene cause glycogen storage disease in Hungarian patients.. PubMed. 5(4). 191–5. 13 indexed citations

20.

Narkis, Ginat, et al.. (1997). Molecular basis of heat labile hexosaminidase B among Jews and Arabs. Human Mutation. 10(6). 424–429. 13 indexed citations

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.

Explore authors with similar magnitude of impact