Ruth Shomrat

982 total citations
36 papers, 637 citations indexed

About

Ruth Shomrat is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Genetics. According to data from OpenAlex, Ruth Shomrat has authored 36 papers receiving a total of 637 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 11 papers in Pathology and Forensic Medicine and 8 papers in Genetics. Recurrent topics in Ruth Shomrat's work include Genetic factors in colorectal cancer (8 papers), Muscle Physiology and Disorders (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Ruth Shomrat is often cited by papers focused on Genetic factors in colorectal cancer (8 papers), Muscle Physiology and Disorders (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Ruth Shomrat collaborates with scholars based in Israel, United States and India. Ruth Shomrat's co-authors include Avi Orr‐Urtreger, Cyril Legum, Yuval Yaron, Paul Rozen, Tova Naiman, Dani Bercovich, Hana Strul, Bruria Ben Zeev, Edward M. Kosower and Yehudit Zipser and has published in prestigious journals such as Gastroenterology, Cancer and Gut.

In The Last Decade

Ruth Shomrat

34 papers receiving 625 citations

Peers

Ruth Shomrat

GENET

PFM

ONCOL

Diane Allingham‐Hawkins Canada

Annalisa Vetro Italy

Marta Albajar Spain

S Staddon United Kingdom

Pauline Terhal Netherlands

Aggeliki Papadopoulou Greece

Rebecca I. Torene United States

Kit San Yeung Hong Kong

Marja Hietala Finland

Judith A. Hobert United States

Diane Allingham‐Hawkins Canada

Ruth Shomrat

283 ×1.0

371 ×1.7

GENET

92 ×0.5

PFM

64 ×0.5

ONCOL

38 ×0.5

Citations per year, relative to Ruth Shomrat Ruth Shomrat (= 1×) peers Diane Allingham‐Hawkins

Countries citing papers authored by Ruth Shomrat

Since Specialization

Citations

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

Fields of papers citing papers by Ruth Shomrat

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruth Shomrat

This figure shows the co-authorship network connecting the top 25 collaborators of Ruth Shomrat. A scholar is included among the top collaborators of Ruth Shomrat 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 Ruth Shomrat. Ruth Shomrat 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

Weiss, Karin, Avi Orr‐Urtreger, Tova Naiman, et al.. (2014). Ethnic effect on FMR1 carrier rate and AGG repeat interruptions among Ashkenazi women. Genetics in Medicine. 16(12). 940–944. 10 indexed citations

Blumkin, Lubov, Sara Kivity, Dorit Lev, et al.. (2012). A compound heterozygous missense mutation and a large deletion in the KCTD7 gene presenting as an opsoclonus-myoclonus ataxia-like syndrome. Journal of Neurology. 259(12). 2590–2598. 35 indexed citations

Ben‐Shachar, Shay, et al.. (2011). Large-scale population screening for spinal muscular atrophy: Clinical implications. Genetics in Medicine. 13(2). 110–114. 31 indexed citations

Landau, Zohar, Aaron Hanukoglu, Joseph Sack, et al.. (2009). Clinical and genetic heterogeneity of congenital adrenal hypoplasia due to NR0B1 gene mutations. Clinical Endocrinology. 72(4). 448–454. 41 indexed citations

Gil, Ziv, et al.. (2007). Cytogenetic analysis of 101 skull base tumors. Head & Neck. 30(5). 567–581. 6 indexed citations

Malcov, Mira, Tamar Schwartz, Ami Amit, et al.. (2004). Multiplex Nested PCR for Preimplantation Genetic Diagnosis of Spinal Muscular Atrophy. Fetal Diagnosis and Therapy. 19(2). 199–206. 19 indexed citations

Lehavi, Ofer, Orna Aizenstein, Dani Bercovich, et al.. (2003). Screening for Familial Dysautonomia in Israel: Evidence for Higher Carrier Rate among Polish Ashkenazi Jews. Genetic Testing. 7(2). 139–142. 35 indexed citations

Shalitin, Shlomit, Ζ. Josefsberg, Éric Vilain, Ruth Shomrat, & Naomi Weintrob. (2002). Adrenal hypoplasia congenita with multiple pituitary hormone deficiency without documented mutation in DAX1 or SF1 gene. Molecular Genetics and Metabolism. 76(2). 157–161. 5 indexed citations

Yaron, Yuval, Bruria Ben Zeev, Ruth Shomrat, et al.. (2002). MECP2 Mutations in Israel: Implications for molecular analysis, genetic counseling, and prenatal diagnosis in Rett syndrome. Human Mutation. 20(4). 323–324. 25 indexed citations

10.

Gavert, Nancy, Yuval Yaron, Tova Naiman, et al.. (2002). Molecular analysis of the APC gene in 71 Israeli families: 17 novel mutations. Human Mutation. 19(6). 664–664. 33 indexed citations

11.

Rozen, Paul, Tova Naiman, Hana Strul, et al.. (2002). Clinical and screening implications of the I1307K adenomatous polyposis coli gene variant in Israeli Ashkenazi Jews with familial colorectal neoplasia. Cancer. 94(10). 2561–2568. 30 indexed citations

12.

Nevo, Yoram, Yuval Yaron, Merav Kedmi, et al.. (2001). Novel mutations in theemerin gene in Israeli families. Human Mutation. 17(6). 522–522. 6 indexed citations

13.

Geva, Eli, et al.. (2000). The Risk of Fragile X Premutation Expansion Is Lower in Carriers Detected by General Prenatal Screening Than in Carriers from Known Fragile X Families. Genetic Testing. 4(3). 289–292. 22 indexed citations

14.

Rozen, Paul, Ruth Shomrat, Hana Strul, et al.. (1999). Prevalence of the I1307K APC gene variant in Israeli Jews of differing ethnic origin and risk for colorectal cancer. Gastroenterology. 116(1). 54–57. 60 indexed citations

15.

Nevo, Yoram, Ruth Shomrat, Yuval Yaron, et al.. (1999). Fetal muscle biopsy as a diagnostic tool in Duchenne muscular dystrophy. Prenatal Diagnosis. 19(10). 921–926. 6 indexed citations

16.

Rozen, Paul, et al.. (1999). Notable intrafamilial phenotypic variability in a kindred with familial adenomatous polyposis and an APC mutation in exon 9. Gut. 45(6). 829–833. 49 indexed citations

17.

Shomrat, Ruth, et al.. (1998). High Frequency of a Common Bloom Syndrome Ashkenazi Mutation Among Jews of Polish Origin. Genetic Testing. 2(4). 293–296. 41 indexed citations

18.

Legum, Cyril, Ruth Shomrat, M.J. Glassner, & Yosef Shiloh. (1994). A molecular survey of Israeli Duchenne and Becker muscular dystrophy patients. Biomedicine & Pharmacotherapy. 48(8-9). 359–364. 1 indexed citations

19.

Shomrat, Ruth, et al.. (1994). Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients. American Journal of Medical Genetics. 49(4). 369–373. 25 indexed citations

20.

Brusel, Marina, Ora Fuchs, Ruth Shomrat, et al.. (1993). Detection of Duchenne muscular dystrophy gene products in amniotic fluid and chorionic villus sampling cells. FEBS Letters. 335(2). 223–230. 3 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.

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