Hagit Baris

3.3k citations

49 papers · 965 indexed · h-index 17

Co-authors: Ian J. Cohen Pramod K. Mistry Wen‐Hann Tan Virginia Kimonis Vivian E. Shih P. Ellen Grant Kalpathy S. Krishnamoorthy Florian Eichler
Topics: Lysosomal Storage Disorders Research (14 papers)Genetic factors in colorectal cancer (10 papers)Carbohydrate Chemistry and Synthesis (7 papers)
Cited by: Physiology Cell Biology Pathology and Forensic Medicine
Journals: Gastroenterology PEDIATRICS Scientific Reports
Partner nations: Israel United States United Kingdom

In The Last Decade

Hagit Baris

48 papers receiving 933 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	ERK Activity in Immature Leukemic Cells Drives Clonal Selection during Induction Therapy for Acute Myeloid Leukemia 2020 ·Scientific Reports ·(unknown),(unknown),(unknown),Dvora Sahar,Dina Rosenberg,(unknown),(unknown),Hagit Baris,(unknown),Igal Louria‐Hayon,Yishai Ofran	5
2	Identification of a novel PCNT founder pathogenic variant in the Israeli Druze population 2019 ·European Journal of Medical Genetics ·Karin Weiss,Nina Ekhilevitch,Lior Cohen,(unknown),Rachel Bello,Ariel F. Martinez,Yarin Hadid,Liran I. Shlush,Alina Kurolap,Tamar Paperna,Adi Mory,Hagit Baris,Maximilian Muenke	6
3	Prenatal microarray analysis in right aortic arch—a retrospective cohort study and review of the literature 2018 ·Journal of Perinatology ·Idit Maya,Amihood Singer,Hagit Baris,Yael Goldberg,Adel Shalata,Morad Khayat,Shay Ben‐Shachar,Lena Sagi‐Dain	14
4	Microarray analysis in pregnancies with isolated unilateral kidney agenesis 2018 ·Pediatric Research ·Lena Sagi‐Dain,Idit Maya,Amir Peleg,Adi Reches,Ehud Banne,Hagit Baris,Tamar Tenne,Amihood Singer,Shay Ben‐Shachar	10
5	Rare Disease Diagnostics: A Single-center Experience and Lessons Learnt 2018 ·Rambam Maimonides Medical Journal ·Karin Weiss,Alina Kurolap,Tamar Paperna,Adi Mory,(unknown),Tova Hershkovitz,Nina Ekhilevitch,Hagit Baris	4
6	Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and Surveillance 2017 ·Gastroenterology ·Sari Lieberman,Tom Walsh,(unknown),Tomer Adar,Eran Goldin,Rachel Beeri,(unknown),Hagit Baris,(unknown),Elizabeth Half,Israela Lerer,Brian H. Shirts,Colin C. Pritchard,Ian Tomlinson,Mary‐Claire King,Ephrat Levy‐Lahad,Tamar Peretz,Yael Goldberg	25
7	Constitutional mismatch repair deficiency and Lynch syndrome among consecutive Arab Bedouins with colorectal cancer in Israel 2017 ·Familial Cancer ·Naim Abu‐Freha,Yaara Leibovici‐Weissman,Alexander Fich,Inbal Kedar,Marisa Halpern,(unknown),Doron M. Behar,(unknown),Alex Vilkin,Hagit Baris,(unknown),Flavio Lejbkowicz,Yaron Niv,Yael Goldberg,Zohar Levi	6
8	Loss of Glycine Transporter 1 Causes a Subtype of Glycine Encephalopathy with Arthrogryposis and Mildly Elevated Cerebrospinal Fluid Glycine 2016 ·The American Journal of Human Genetics ·Alina Kurolap,(unknown),Tova Hershkovitz,(unknown),Adi Mory,Tamar Paperna,Ewald Hannappel,Galit Tal,(unknown),(unknown),Muhammad Mahajnah,Anat Ilivitzki,Dov Hershkovitz,Nina Ekhilevitch,Hanna Mandel,Volker Eulenburg,Hagit Baris	25
9	Trio approach reveals higher risk of PD in carriers of severe vs. mild GBA mutations 2016 ·Blood Cells Molecules and Diseases ·David Arkadir,Tama Dinur,Stephen Mullin,Atul Mehta,Hagit Baris,Roy N. Alcalay,Ari Zimran	16
10	13,845 home therapy infusions with velaglucerase alfa exemplify safety of velaglucerase alfa and increased compliance to every-other-week intravenous enzyme replacement therapy for Gaucher disease 2015 ·Blood Cells Molecules and Diseases ·Deborah Elstein,Aya Abrahamov,(unknown),(unknown),Hagit Baris,Ari Zimran	12
11	Non-syndromic retinitis pigmentosa due to mutations in the mucopolysaccharidosis type IIIC gene, heparan-alpha-glucosaminide N-acetyltransferase (HGSNAT) 2015 ·Human Molecular Genetics ·Lonneke Haer‐Wigman,Horatio Hackett Newman,Rina Leibu,Nathalie M. Bax,Hagit Baris,(unknown),Eyal Banin,(unknown),Susanne Roosing,Dirk J. Lefeber,Marijke N. Zonneveld-Vrieling,Ofer Isakov,Noam Shomron,Dror Sharon,Anneke I. den Hollander,Carel B. Hoyng,Frans P.M. Cremers,Tamar Ben‐Yosef	53
12	Lynch Syndrome in high risk Ashkenazi Jews in Israel 2013 ·Familial Cancer ·Yael Goldberg,Inbal Kedar,(unknown),Naama Halpern,(unknown),Ayala Hubert,Luna Kaduri,Michal Sagi,Israela Lerer,Dvorah Abeliovich,Tamar Hamburger,Aviram Nissan,Hanoch Goldshmidt,(unknown),Ravit Geva,Hana Strul,Guy Rosner,Hagit Baris,Zohar Levi,Tamar Peretz	16
13	X inactivation testing for identifying a non-syndromic X-linked mental retardation gene 2011 ·Journal of Applied Genetics ·Hagith Yonath,Dina Marek‐Yagel,(unknown),(unknown),Hagit Baris,Mordechai Shohat,Moshe Frydman,Elon Pras	4
14	Upper and Lower Gastrointestinal Findings in PTEN Mutation–Positive Cowden Syndrome Patients Participating in an Active Surveillance Program 2011 ·Clinical and Translational Gastroenterology ·Zohar Levi,Hagit Baris,Inbal Kedar,Yaron Niv,Alex Geller,Eyal Gal,(unknown),Sara Morgenstern,(unknown),Brandie Heald,Mary P. Bronner,Charis Eng	43
15	Autosomal dominant syndrome of mental retardation, hypotelorism, and cleft palate resembling Schilbach–Rott syndrome 2009 ·American Journal of Medical Genetics Part A ·(unknown),Hagit Baris,Gavriel Gal,(unknown),Shlomo Calderon,Marja W. Wessels,Anneke Maat‐Kievit,Björn Menten,Elfride De Baere,Raoul C. M. Hennekam,Anja Schirmacher,Sherri J. Bale,Mordechai Shohat,Patrick J. Willems	4
16	A novelGJB6missense mutation in hidrotic ectodermal dysplasia 2 (Clouston syndrome) broadens its genotypic basis 2008 ·British Journal of Dermatology ·Hagit Baris,(unknown),(unknown),Victoria Doviner,M. Shohat,Haike Reznik‐Wolf,Eran Pras	16
17	Diagnostic utility of array‐based comparative genomic hybridization in a clinical setting 2007 ·American Journal of Medical Genetics Part A ·Hagit Baris,Wen‐Hann Tan,Virginia Kimonis,Mira Irons	25
18	Identification of a novel polymorphism—the duplication of the NPHP1 (nephronophthisis 1) gene 2006 ·American Journal of Medical Genetics Part A ·Hagit Baris,Bassem A. Bejjani,Wen‐Hann Tan,David L. Coulter,Judith A. Martin,Andrea L. Storm,Barbara K. Burton,Sulagna C. Saitta,Marzena Gajęcka,Blake C. Ballif,Mira Irons,Lisa G. Shaffer,Virginia Kimonis	13
19	Cockayne syndrome: The developing phenotype 2005 ·American Journal of Medical Genetics Part A ·Wen‐Hann Tan,Hagit Baris,Caroline D. Robson,Virginia Kimonis	10
20	Hypothelia, syndactyly, and ear malformation?a variant of the scalp-ear-nipple syndrome?: Case report and review of the literature 2005 ·American Journal of Medical Genetics Part A ·Hagit Baris,Wen‐Hann Tan,Virginia Kimonis	4

About Hagit Baris

Hagit Baris is a scholar working on Pathology and Forensic Medicine, Genetics and Physiology, having authored 49 papers that have together received 965 indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (14 papers), Genetic factors in colorectal cancer (10 papers) and Carbohydrate Chemistry and Synthesis (7 papers). The work is most often cited by research in Physiology (327 citations), Cell Biology (163 citations) and Pathology and Forensic Medicine (158 citations). Hagit Baris has collaborated with scholars based in Israel, United States and United Kingdom. Frequent 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. Their work appears in journals such as Gastroenterology, PEDIATRICS and Scientific Reports.

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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