Ruth Gershoni‐Baruch

11.7k citations

145 papers · 6.1k indexed · h-index 39

Molecular Biology top 2%
Genetics top 1%
Immunology top 2%
Oncology top 5%
Nephrology top 1%

Co-authors: Riva Brik Judith Aharon‐Peretz Hanna Rosenbaum Marwan Shinawi Amos Etzioni Eitan Friedman Efrat Dagan L Kasinetz
Topics: BRCA gene mutations in cancer (24 papers)Inflammasome and immune disorders (18 papers)DNA Repair Mechanisms (12 papers)
Cited by: Nephrology Immunology and Allergy Genetics
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences Journal of Clinical Investigation
Partner nations: Israel United States Canada

In The Last Decade

Ruth Gershoni‐Baruch

144 papers receiving 5.9k citations

Peers

Countries citing papers authored by Ruth Gershoni‐Baruch

Since Specialization

Citations

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

Fields of papers citing papers by Ruth Gershoni‐Baruch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruth Gershoni‐Baruch

This figure shows the co-authorship network connecting the top 25 collaborators of Ruth Gershoni‐Baruch. A scholar is included among the top collaborators of Ruth Gershoni‐Baruch 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 Gershoni‐Baruch. Ruth Gershoni‐Baruch 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 missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred 2013 ·European Journal of Human Genetics ·Adi Mory,Francesc X. Ruiz,Efrat Dagan,(unknown),Alina Kurolap,Xavier Parés,Jaume Farrés,Ruth Gershoni‐Baruch	22
2	MEFV, TNFRSF1A and CARD15 mutation analysis in Behçet's disease. 2011 ·PubMed ·(unknown),Efrat Dagan,Itzhak Rosner,Massimo Fiorilli,Ruth Gershoni‐Baruch,Michael Rozenbaum	9
3	Vascular Behcet and Mutations in Thrombogenic Genes: Methylene Tetrahydrofolate Reductase, Factor V, and Prothrombin 2011 ·Genetic Testing and Molecular Biomarkers ·Efrat Dagan,(unknown),Massimo Fiorilli,Michael Rozenbaum,Itzhak Rosner,Ruth Gershoni‐Baruch	8
4	‘Pure’ partial trisomy 11q (11q23.1→11qter) 2011 ·Clinical Dysmorphology ·(unknown),Tatiana Smolkin,(unknown),(unknown),Shraga Blazer,Ruth Gershoni‐Baruch,Imad R. Makhoul	10
5	Molecular Epidemiology of Hereditary Epidermolysis Bullosa in a Middle Eastern Population 2006 ·Journal of Investigative Dermatology ·(unknown),Margarita Indelman,Ellen G Pfendner,Tzipora C. Falik‐Zaccai,(unknown),Stavit A. Shalev,(unknown),(unknown),(unknown),(unknown),Ruth Gershoni‐Baruch,Morad Khayat,(unknown),Gabriele Richard,Richard N. Bergman,Jouni Uitto,Moien Kanaan,Eli Sprecher	42
6	Henoch–Schonlein purpura: polymorphisms in thrombophilia genes 2006 ·Pediatric Nephrology ·Efrat Dagan,Riva Brik,(unknown),Ruth Gershoni‐Baruch	8
7	Autosomal recessive Oliver–McFarlane syndrome: Retinitis pigmentosa, short stature (GH deficiency), trichomegaly, and hair anomalies or CPD syndrome (chorioretinopathy‐pituitary dysfunction) 2005 ·American Journal of Medical Genetics Part A ·Motti Haimi,Ruth Gershoni‐Baruch	10
8	Coinheritance ofBRCA1 andBRCA2 mutations with Fanconi anemia and Bloom syndrome mutations in Ashkenazi Jewish population: Possible role in risk modification for cancer development 2005 ·American Journal of Hematology ·Maya Koren‐Michowitz,Eitan Friedman,Ruth Gershoni‐Baruch,F. Brok‐Simoni,(unknown),Gideon Rechavi,(unknown)	7
9	Breast-feeding and the Risk of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers 2004 ·JNCI Journal of the National Cancer Institute ·Helena Jernström,Jan Lubiński,Henry T. Lynch,P Ghadirian,Susan L. Neuhausen,Claudine Isaacs,Barbara L. Weber,Doug Horsman,Barry P. Rosen,William D. Foulkes,Eitan Friedman,Ruth Gershoni‐Baruch,Peter Ainsworth,M. Daly,Judy E. Garber,Håkan Olsson,Peng Sun,Steven A. Narod	135
10	The contribution of genotypes at the MEFV and SAA1 loci to amyloidosis and disease severity in patients with familial Mediterranean fever 2003 ·Arthritis & Rheumatism ·Ruth Gershoni‐Baruch,Riva Brik,(unknown),Marwan Shinawi,Merav Lidar,Avi Livneh	135
11	Leukocyte adhesion deficiency (LAD) type II/carbohydrate deficient glycoprotein (CDG) IIc founder effect and genotype/phenotype correlation 2002 ·American Journal of Medical Genetics ·Amos Etzioni,Laura Sturla,Anthony Antonellis,Eric D. Green,Ruth Gershoni‐Baruch,Patricia Berninsone,Carlos B. Hirschberg,Michela Tonetti	57
12	The musculoskeletal manifestations of familial Mediterranean fever in children genetically diagnosed with the disease 2001 ·Arthritis & Rheumatism ·Riva Brik,Marwan Shinawi,L Kasinetz,Ruth Gershoni‐Baruch	66
13	Caudal dysplasia sequence with penile enlargement: Case report and a potential pathogenic hypothesis 2001 ·American Journal of Medical Genetics ·Imad R. Makhoul,Ayala Aviram‐Goldring,Tamar Paperna,Polo Sujov,Shlomit Rienstein,Tatiana Smolkin,Mónica Epelman,Ruth Gershoni‐Baruch	5
14	Familial Mediterranean fever: high gene frequency and heterogeneous disease among an Israeli-Arab population. 2000 ·PubMed ·Marwan Shinawi,R Brik,Moshe Berant,L Kasinetz,Ruth Gershoni‐Baruch	35
15	Common origin of the I1307K APC polymorphism in Ashkenazi and non-Ashkenazi Jews 1999 ·European Journal of Human Genetics ·(unknown),Arié Figer,Ruth Gershoni‐Baruch,Moshe Z. Papa,(unknown),Rakefet Chen‐Shtoyerman,Avraham Karasik,Livia Theodor,Eitan Friedman	15
16	BRCA1 and BRCA2 founder mutations in patients with bilateral breast cancer 1999 ·European Journal of Human Genetics ·Ruth Gershoni‐Baruch,Efrat Dagan,(unknown),Ilana Kepten,Eliezer Robinson	25
17	The D allele of the angiotensin-converting enzyme gene contributes towards blood LDL-cholesterol levels and the presence of hypertension 1999 ·Atherosclerosis ·Ilana Oren,J.G. Brook,Ruth Gershoni‐Baruch,Ilana Kepten,(unknown),Shai Linn,Efrat Wolfovitz	24
18	Leukocyte adhesion deficiency type II: Long-term follow-up 1998 ·Journal of Allergy and Clinical Immunology ·Amos Etzioni,Ruth Gershoni‐Baruch,Shimon Pollack,Naim Shehadeh	27
19	Markedly Elevated Alpha-Fetoprotein and Positive Acetylcholinesterase in Amniotic Fluid from a Pregnancy Affected with Dystrophic Epidermolysis bullosa 1995 ·Fetal Diagnosis and Therapy ·A Drugan,(unknown),Polo Sujov,Ruth Gershoni‐Baruch	6
20	Saethre‐Chotzen Syndrome Associated with Defective Neutrophil Chemotaxis 1990 ·Acta Paediatrica ·Amos Etzioni,(unknown),A Benderly,Ruth Gershoni‐Baruch	5

About Ruth Gershoni‐Baruch

Ruth Gershoni‐Baruch is a scholar working on Genetics, Immunology and Allergy and Molecular Biology, having authored 145 papers that have together received 6.1k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (24 papers), Inflammasome and immune disorders (18 papers) and DNA Repair Mechanisms (12 papers). The work is most often cited by research in Nephrology (607 citations), Immunology and Allergy (436 citations) and Genetics (1.7k citations). Ruth Gershoni‐Baruch has collaborated with scholars based in Israel, United States and Canada. Frequent co-authors include Riva Brik, Judith Aharon‐Peretz, Hanna Rosenbaum, Marwan Shinawi, Amos Etzioni, Eitan Friedman, Efrat Dagan, L Kasinetz, Avi Livneh and Moshe Frydman. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Journal of Clinical Investigation.

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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