Hagit Baris

3.3k total citations
49 papers, 965 citations indexed

About

Hagit Baris is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Hagit Baris has authored 49 papers receiving a total of 965 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 16 papers in Genetics and 14 papers in Physiology. Recurrent topics in Hagit Baris's work include Lysosomal Storage Disorders Research (14 papers), Genetic factors in colorectal cancer (10 papers) and Carbohydrate Chemistry and Synthesis (7 papers). Hagit Baris is often cited by papers focused on Lysosomal Storage Disorders Research (14 papers), Genetic factors in colorectal cancer (10 papers) and Carbohydrate Chemistry and Synthesis (7 papers). Hagit Baris collaborates with scholars based in Israel, United States and United Kingdom. Hagit Baris's co-authors include Ian J. Cohen, Pramod K. Mistry, Wen‐Hann Tan, Virginia Kimonis, Vivian E. Shih, P. Ellen Grant, Kalpathy S. Krishnamoorthy, Florian Eichler, Yael Goldberg and Zohar Levi and has published in prestigious journals such as Gastroenterology, PEDIATRICS and Scientific Reports.

In The Last Decade

Hagit Baris

48 papers receiving 933 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Hagit Baris Israel 17 385 327 203 163 158 49 965
C B Whitley United States 17 287 0.7× 556 1.7× 138 0.7× 143 0.9× 76 0.5× 30 970
Weston P. Miller United States 25 814 2.1× 484 1.5× 211 1.0× 62 0.4× 70 0.4× 72 1.7k
Suma P. Shankar United States 21 833 2.2× 628 1.9× 180 0.9× 282 1.7× 80 0.5× 71 1.5k
Rachel Laframboise Canada 25 974 2.5× 227 0.7× 544 2.7× 116 0.7× 125 0.8× 57 1.7k
Motomichi Kosuga Japan 19 239 0.6× 500 1.5× 157 0.8× 89 0.5× 43 0.3× 54 839
Michele R. Filling‐Katz United States 13 294 0.8× 369 1.1× 99 0.5× 88 0.5× 88 0.6× 22 908
P Guibaud France 19 548 1.4× 349 1.1× 138 0.7× 75 0.5× 81 0.5× 60 1.1k
Virginia K. Proud United States 17 549 1.4× 117 0.4× 320 1.6× 114 0.7× 50 0.3× 32 1.1k
Leena Peltonen Finland 8 295 0.8× 155 0.5× 311 1.5× 76 0.5× 95 0.6× 9 935
Yasutsugu Chinen Japan 15 269 0.7× 371 1.1× 209 1.0× 97 0.6× 26 0.2× 38 736

Countries citing papers authored by Hagit Baris

Since Specialization
Citations

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

Fields of papers citing papers by Hagit Baris

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hagit Baris

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

All Works

20 of 20 papers shown
1.
Sahar, Dvora, et al.. (2020). ERK Activity in Immature Leukemic Cells Drives Clonal Selection during Induction Therapy for Acute Myeloid Leukemia. Scientific Reports. 10(1). 8349–8349. 5 indexed citations
2.
Weiss, Karin, Nina Ekhilevitch, Lior Cohen, et al.. (2019). Identification of a novel PCNT founder pathogenic variant in the Israeli Druze population. European Journal of Medical Genetics. 63(2). 103643–103643. 6 indexed citations
3.
Maya, Idit, Amihood Singer, Hagit Baris, et al.. (2018). Prenatal microarray analysis in right aortic arch—a retrospective cohort study and review of the literature. Journal of Perinatology. 38(5). 468–473. 14 indexed citations
4.
Sagi‐Dain, Lena, Idit Maya, Amir Peleg, et al.. (2018). Microarray analysis in pregnancies with isolated unilateral kidney agenesis. Pediatric Research. 83(4). 825–828. 10 indexed citations
5.
Weiss, Karin, Alina Kurolap, Tamar Paperna, et al.. (2018). Rare Disease Diagnostics: A Single-center Experience and Lessons Learnt. Rambam Maimonides Medical Journal. 9(3). e0018–e0018. 4 indexed citations
6.
Lieberman, Sari, Tom Walsh, Tomer Adar, et al.. (2017). Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance. Gastroenterology. 152(8). 1876–1880.e1. 25 indexed citations
7.
Abu‐Freha, Naim, Yaara Leibovici‐Weissman, Alexander Fich, et al.. (2017). Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel. Familial Cancer. 17(1). 79–86. 6 indexed citations
8.
Kurolap, Alina, Tova Hershkovitz, Adi Mory, et al.. (2016). Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine. The American Journal of Human Genetics. 99(5). 1172–1180. 25 indexed citations
9.
Arkadir, David, Tama Dinur, Stephen Mullin, et al.. (2016). Trio approach reveals higher risk of PD in carriers of severe vs. mild GBA mutations. Blood Cells Molecules and Diseases. 68. 115–116. 16 indexed citations
10.
11.
Haer‐Wigman, Lonneke, Horatio Hackett Newman, Rina Leibu, et al.. (2015). Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT). Human Molecular Genetics. 24(13). 3742–51. 53 indexed citations
12.
Goldberg, Yael, Inbal Kedar, Naama Halpern, et al.. (2013). Lynch Syndrome in high risk Ashkenazi Jews in Israel. Familial Cancer. 13(1). 65–73. 16 indexed citations
13.
Yonath, Hagith, Dina Marek‐Yagel, Hagit Baris, et al.. (2011). X inactivation testing for identifying a non-syndromic X-linked mental retardation gene. Journal of Applied Genetics. 52(4). 437–441. 4 indexed citations
14.
Levi, Zohar, Hagit Baris, Inbal Kedar, et al.. (2011). Upper and Lower Gastrointestinal Findings in PTEN Mutation–Positive Cowden Syndrome Patients Participating in an Active Surveillance Program. Clinical and Translational Gastroenterology. 2(11). e5–e5. 43 indexed citations
15.
Baris, Hagit, Gavriel Gal, Shlomo Calderon, et al.. (2009). Autosomal dominant syndrome of mental retardation, hypotelorism, and cleft palate resembling Schilbach–Rott syndrome. American Journal of Medical Genetics Part A. 149A(12). 2700–2705. 4 indexed citations
16.
Baris, Hagit, et al.. (2008). A novelGJB6missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis. British Journal of Dermatology. 159(6). 1373–1376. 16 indexed citations
17.
Baris, Hagit, Wen‐Hann Tan, Virginia Kimonis, & Mira Irons. (2007). Diagnostic utility of array‐based comparative genomic hybridization in a clinical setting. American Journal of Medical Genetics Part A. 143A(21). 2523–2533. 25 indexed citations
18.
Baris, Hagit, Bassem A. Bejjani, Wen‐Hann Tan, et al.. (2006). Identification of a novel polymorphism—the duplication of the NPHP1 (nephronophthisis 1) gene. American Journal of Medical Genetics Part A. 140A(17). 1876–1879. 13 indexed citations
19.
Tan, Wen‐Hann, Hagit Baris, Caroline D. Robson, & Virginia Kimonis. (2005). Cockayne syndrome: The developing phenotype. American Journal of Medical Genetics Part A. 135A(2). 214–216. 10 indexed citations
20.
Baris, Hagit, Wen‐Hann Tan, & Virginia Kimonis. (2005). Hypothelia, syndactyly, and ear malformation?a variant of the scalp-ear-nipple syndrome?: Case report and review of the literature. American Journal of Medical Genetics Part A. 134A(2). 220–222. 4 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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