Nurit Magal

2.5k citations

51 papers · 1.7k indexed · h-index 21

Co-authors: Mordechai Shohat Lina Basel‐Vanagaite Gabrielle J. Halpern Valerie Drasinover Ellen Taub Yehuda L. Danon Metsada Pasmanik‐Chor Nathan Fischel‐Ghodsian
Topics: Genetic Neurodegenerative Diseases (7 papers)Inflammasome and immune disorders (6 papers)Genomics and Rare Diseases (5 papers)
Cited by: Nephrology Genetics Molecular Biology
Journals: Circulation Journal of Clinical Investigation Neurology
Partner nations: Israel United States Germany

In The Last Decade

Nurit Magal

51 papers receiving 1.6k citations

Peers

Countries citing papers authored by Nurit Magal

Since Specialization

Citations

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

Fields of papers citing papers by Nurit Magal

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nurit Magal

This figure shows the co-authorship network connecting the top 25 collaborators of Nurit Magal. A scholar is included among the top collaborators of Nurit Magal 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 Nurit Magal. Nurit Magal 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	A nonsense variant in the second exon of the canonical transcript of NSD1 does not cause Sotos syndrome 2021 ·American Journal of Medical Genetics Part A ·Noa Ruhrman‐Shahar,Nurit Assia Batzir,Gabriel Lidzbarsky,Lily Bazak,Nurit Magal,Lina Basel‐Vanagaite	1
2	When phenotype does not match genotype: importance of “real-time” refining of phenotypic information for exome data interpretation 2020 ·Genetics in Medicine ·Lina Basel‐Vanagaite,Noa Ruhrman‐Shahar,Naama Orenstein,Yael Goldberg,Claudia Gonzaga‐Jauregui,Alan R. Shuldiner,Rivka Sukenik‐Halevy,Idit Maya,Nurit Magal,(unknown),(unknown),Gabriel Lidzbarsky,Lily Bazak	14
3	Improved diagnostics by exome sequencing following raw data reevaluation by clinical geneticists involved in the medical care of the individuals tested 2018 ·Genetics in Medicine ·Lina Basel‐Vanagaite,Naama Orenstein,(unknown),Noa Ruhrman‐Shahar,(unknown),Nurit Magal,Monika Weisz Hubshman,Lily Bazak	55
4	Mutations in ERGIC1 cause Arthrogryposis multiplex congenita, neuropathic type 2017 ·Clinical Genetics ·Eyal Reinstein,Valerie Drasinover,Rachel Lotan,(unknown),Iftach Nachman,Eran Eyal,Lutfi Jaber,Nurit Magal,M Shohat	8
5	A de novo GABRA2 missense mutation in severe early-onset epileptic encephalopathy with a choreiform movement disorder 2017 ·European Journal of Paediatric Neurology ·Naama Orenstein,Hadassa Goldberg‐Stern,Rachel Straussberg,Lily Bazak,Monika Weisz Hubshman,(unknown),Oded Gilad,Oded Scheuerman,(unknown),(unknown),Shay Tzur,Nurit Magal,(unknown),(unknown),Lina Basel‐Vanagaite	23
6	Identification of a novel mutation in the PNLIP gene in two brothers with congenital pancreatic lipase deficiency 2013 ·Journal of Lipid Research ·Doron M. Behar,Lina Basel‐Vanagaite,Fabian Glaser,Marielle Kaplan,Shay Tzur,Nurit Magal,Tal Eidlitz‐Markus,Y. Cohen,Galit Sarig,Concetta Bormans,Mordechai Shohat,Avraham Zeharia	24
7	Multiple congenital anomalies-hypotonia-seizures syndrome is caused by a mutation in PIGN 2011 ·Journal of Medical Genetics ·(unknown),Iris Noyman,Adi Har‐Zahav,Ziva Ben Neriah,Metsada Pasmanik‐Chor,Adva Yeheskel,(unknown),Idit Maya,Nurit Magal,Einat Birk,Anthony Simon,Anat Halevy,Gidi Rechavi,Mordechai Shohat,Rachel Straussberg,Lina Basel‐Vanagaite	112
8	Large-Scale Population Carrier Screening for Spinal Muscular Atrophy in Israel—Effect of Ethnicity on the False-Negative Rate 2010 ·Genetic Testing and Molecular Biomarkers ·Rivka Sukenik‐Halevy,(unknown),(unknown),Nurit Magal,Mordechai Shohat	6
9	Genetic Carrier Screening for Spinal Muscular Atrophy and Spinal Muscular Atrophy with Respiratory Distress 1 in an Isolated Population in Israel 2008 ·Genetic Testing ·Lina Basel‐Vanagaite,Ellen Taub,Valerie Drasinover,Nurit Magal,(unknown),Joël Zlotogora,Mordechai Shohat	22
10	Identification of the gene causing long QT syndrome in an Israeli family. 2008 ·PubMed ·(unknown),Shahar Lavi,Nurit Magal,Gabrielle J. Halpern,(unknown),Monther Boulos,Michael Kapeliovich,Mordechai Shohat,Haim Hammerman	2
11	Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype 2008 ·Clinical Genetics ·Limor Avrahami,Saskia M. Maas,Metsada Pasmanik‐Chor,(unknown),Nurit Magal,(unknown),Jan van Marle,M Shohat,Lina Basel‐Vanagaite	40
12	Autosomal Recessive Ichthyosis with Hypotrichosis Caused by a Mutation in ST14, Encoding Type II Transmembrane Serine Protease Matriptase 2007 ·The American Journal of Human Genetics ·Lina Basel‐Vanagaite,(unknown),Akemi Ishida‐Yamamoto,(unknown),Dan Ben Amitai,Raziel Lurie,Metsada Pasmanik‐Chor,Margarita Indelman,Alex Zvulunov,(unknown),Nurit Magal,Eli Sprecher,Mordechai Shohat	137
13	Mutated nup62 causes autosomal recessive infantile bilateral striatal necrosis 2006 ·Annals of Neurology ·Lina Basel‐Vanagaite,(unknown),Rachel Straussberg,Metsada Pasmanik‐Chor,(unknown),(unknown),Christopher A. Walsh,Nurit Magal,Ellen Taub,Valerie Drasinover,Hanna Shalev,(unknown),Gideon Rechavi,Anthony Simon,Mordechai Shohat	92
14	Fine mapping places the gene for arthrogryposis multiplex congenita neuropathic type between D5S394 and D5S2069 on chromosome 5qter 2001 ·American Journal of Medical Genetics ·(unknown),Nurit Magal,Gabrielle J. Halpern,Lutfi Jaber,Mordechai Shohat	11
15	Increased transmission of intermediate alleles of theFMR1 gene compared with normal alleles among female heterozygotes 2000 ·American Journal of Medical Genetics ·Valerie Drasinover,(unknown),Nurit Magal,Ellen Taub,(unknown),Tamy Shohat,Gabrielle J. Halpern,Mordechai Shohat	14
16	Higher than expected carrier rates for familial Mediterranean fever in various Jewish ethnic groups 2000 ·European Journal of Human Genetics ·Nava Stoffman,Nurit Magal,Tamy Shohat,Rachel Lotan,(unknown),Assaf P. Oron,Yehuda L. Danon,Gabrielle J. Halpern,(unknown),Mordechai Shohat	112
17	Phenotype–genotype correlation in familial Mediterranean fever: evidence for an association between Met694Val and amyloidosis 1999 ·European Journal of Human Genetics ·Mordechai Shohat,Nurit Magal,Tami Shohat,Xi Chen,Tal Dagan,Aviva Mimouni-Bloch,Yehuda L. Danon,Rachel Lotan,Gönül Oğur,Aydan Şirin,(unknown),(unknown),Arthur D. Schwabe,Daniel L. Kastner,JI Rotter,Nathan Fischel‐Ghodsian	167
18	Abnormal Liver Test Results in Myotonic Dystrophy 1998 ·Journal of Clinical Gastroenterology ·Anat Achiron,Yoram Barak,Nurit Magal,(unknown),Michael I. Cohen,(unknown),N Gadoth	26
19	Amyloidosis in Familial Mediterranean Fever Is Associated with a Specific Ancestral Haplotype in the MEFV Locus 1998 ·Molecular Genetics and Metabolism ·M Shohat,Rachel Lotan,Nurit Magal,Yehuda L. Danon,Gönül Oğur,(unknown),(unknown),Arthur D. Schwabe,(unknown),Nathan Fischel‐Ghodsian,Daniel L. Kastner,Tami Shohat,Jerome I. Rotter	6
20	A Gene for Arthrogryposis Multiplex Congenita Neuropathic Type Is Linked to D5S394 on Chromosome 5qter 1997 ·The American Journal of Human Genetics ·Mordechai Shohat,Rona Lotan,Nurit Magal,Tamar Shohat,Nathan Fischel‐Ghodsian,Jerome I. Rotter,Lutfi Jaber	18

About Nurit Magal

Nurit Magal is a scholar working on Genetics, Genetics and Molecular Biology, having authored 51 papers that have together received 1.7k indexed citations. Recurring topics across this work include Genetic Neurodegenerative Diseases (7 papers), Inflammasome and immune disorders (6 papers) and Genomics and Rare Diseases (5 papers). The work is most often cited by research in Nephrology (115 citations), Genetics (439 citations) and Molecular Biology (962 citations). Nurit Magal has collaborated with scholars based in Israel, United States and Germany. Frequent co-authors include Mordechai Shohat, Lina Basel‐Vanagaite, Gabrielle J. Halpern, Valerie Drasinover, Mordechai Shohat, Ellen Taub, Yehuda L. Danon, Metsada Pasmanik‐Chor, Nathan Fischel‐Ghodsian and Bella Davidov. Their work appears in journals such as Circulation, Journal of Clinical Investigation and Neurology.

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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