Hagit Baris Feldman

14.0k total citations
42 papers, 366 citations indexed

About

Hagit Baris Feldman is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Hagit Baris Feldman has authored 42 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 16 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Hagit Baris Feldman's work include BRCA gene mutations in cancer (6 papers), Complement system in diseases (6 papers) and Prenatal Screening and Diagnostics (6 papers). Hagit Baris Feldman is often cited by papers focused on BRCA gene mutations in cancer (6 papers), Complement system in diseases (6 papers) and Prenatal Screening and Diagnostics (6 papers). Hagit Baris Feldman collaborates with scholars based in Israel, United States and Türkiye. Hagit Baris Feldman's co-authors include Alina Kurolap, Adi Mory, Tuvia Gilat, Tamar Paperna, Adi Reches, Claudia Gonzaga‐Jauregui, Yael Goldberg, Tova Hershkovitz, Yuval Yaron and Martine Muleris and has published in prestigious journals such as New England Journal of Medicine, Nucleic Acids Research and Gut.

In The Last Decade

Hagit Baris Feldman

33 papers receiving 350 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 Feldman Israel 11 131 71 67 67 49 42 366
Elena Schnabel‐Besson Germany 8 348 2.7× 110 1.5× 26 0.4× 63 0.9× 29 0.6× 17 582
Soo-Mi Kweon United States 11 318 2.4× 42 0.6× 36 0.5× 25 0.4× 33 0.7× 21 535
Eva Galle Belgium 6 214 1.6× 24 0.3× 35 0.5× 26 0.4× 45 0.9× 7 413
Sara Santos Franco United Kingdom 8 154 1.2× 19 0.3× 31 0.5× 101 1.5× 19 0.4× 10 380
Dangxiao Cheng Canada 13 318 2.4× 66 0.9× 43 0.6× 25 0.4× 75 1.5× 38 589
Elizabeth Yang United States 11 294 2.2× 45 0.6× 68 1.0× 51 0.8× 20 0.4× 33 495
Maria Franca Marongiu Italy 12 142 1.1× 38 0.5× 50 0.7× 209 3.1× 11 0.2× 18 774
Christina Hung United States 11 223 1.7× 84 1.2× 15 0.2× 101 1.5× 21 0.4× 21 370
Johanna Lundin Sweden 9 216 1.6× 91 1.3× 62 0.9× 11 0.2× 19 0.4× 20 397
E Raskopf Germany 16 297 2.3× 26 0.4× 22 0.3× 100 1.5× 43 0.9× 40 636

Countries citing papers authored by Hagit Baris Feldman

Since Specialization
Citations

This map shows the geographic impact of Hagit Baris Feldman'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 Feldman 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 Feldman more than expected).

Fields of papers citing papers by Hagit Baris Feldman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hagit Baris Feldman

This figure shows the co-authorship network connecting the top 25 collaborators of Hagit Baris Feldman. A scholar is included among the top collaborators of Hagit Baris Feldman 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 Feldman. Hagit Baris Feldman 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.
Litcher‐Kelly, Leighann, Ahmet Özen, Hagit Baris Feldman, et al.. (2025). The patient experience of CHAPLE disease: results from interviews conducted as part of a clinical trial for an ultra-rare condition. Orphanet Journal of Rare Diseases. 20(1). 68–68. 1 indexed citations
2.
Hamiel, Uri, Alina Kurolap, Adi Mory, et al.. (2025). Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome. Journal of Genetics. 104(1).
3.
Yaron, Yuval, Michal Berkenstadt, Doron M. Behar, et al.. (2025). Evaluation of the digital genetic assistant in technology assisted genetic counseling for genetic carrier screening. npj Digital Medicine. 8(1). 183–183.
4.
Mory, Adi, Adi Reches, Karina Krajden Haratz, et al.. (2025). Diagnostic Value of Exome Sequencing in Isolated Polyhydramnios. Prenatal Diagnosis.
5.
Kurolap, Alina, et al.. (2024). PUF60 loss‐of‐function with normal cognition should be considered in the differential diagnosis of Klippel–Feil syndrome. American Journal of Medical Genetics Part A. 194(6). e63550–e63550.
6.
Litcher‐Kelly, Leighann, Ahmet Özen, Hagit Baris Feldman, et al.. (2024). Pozelimab for CHAPLE disease: results from in-trial interviews and clinical outcome assessments. Orphanet Journal of Rare Diseases. 19(1). 290–290. 3 indexed citations
7.
Kurolap, Alina, Isaiah D. Wexler, Adi Mory, et al.. (2023). A common benign intronic deletion masking a pathogenic deep intronic PCCB variant - genome sequencing and RNA studies to the rescue. Molecular Genetics and Metabolism. 140(3). 107702–107702. 1 indexed citations
8.
Kurolap, Alina, Adi Mory, Karina Krajden Haratz, et al.. (2023). SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance. Prenatal Diagnosis. 43(10). 1374–1377. 3 indexed citations
9.
Hamiel, Uri, et al.. (2023). Telemedicine Versus Traditional In-Person Consultations: Comparison of Patient Satisfaction Rates. Telemedicine Journal and e-Health. 30(4). 1013–1019. 4 indexed citations
10.
Feldman, Hagit Baris, David Zahler, Adi Mory, et al.. (2023). Corin and Left Atrial Cardiomyopathy, Hypertension, Arrhythmia, and Fibrosis. New England Journal of Medicine. 389(18). 1685–1692. 7 indexed citations
11.
Yaron, Yuval, Adi Mory, Alina Kurolap, et al.. (2022). Exome sequencing as first‐tier test for fetuses with severe central nervous system structural anomalies. Ultrasound in Obstetrics and Gynecology. 60(1). 59–67. 48 indexed citations
12.
Yinon, Yoav, et al.. (2022). Non‐immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing. Prenatal Diagnosis. 42(7). 890–893. 1 indexed citations
13.
Kurolap, Alina, Adi Mory, Karina Krajden Haratz, et al.. (2022). Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharing. Prenatal Diagnosis. 42(12). 1484–1487. 3 indexed citations
14.
German, Alina, Amir Peleg, Claudia Gonzaga‐Jauregui, et al.. (2021). A novel truncating variant in the FGD1 gene associated with Aarskog–Scott syndrome in a family previously diagnosed with Tel Hashomer camptodactyly. American Journal of Medical Genetics Part A. 185(10). 3161–3166.
15.
Mistry, Pramod K., Elena Lukina, Hadhami Ben Turkia, et al.. (2021). Clinical outcomes after 4.5 years of eliglustat therapy for Gaucher disease type 1: Phase 3 ENGAGE trial final results. American Journal of Hematology. 96(9). 1156–1165. 31 indexed citations
16.
Pollack, Shirley, Adi Mory, Tamar Paperna, et al.. (2021). A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case Report. Frontiers in Immunology. 12. 608604–608604. 1 indexed citations
17.
Ekhilevitch, Nina, et al.. (2021). A recurrent pathogenic BRCA2 exon 5–11 duplication in the Christian Arab population in Israel. Familial Cancer. 21(3). 289–294. 1 indexed citations
18.
Hershkovitz, Tova, Alina Kurolap, Galit Tal, et al.. (2020). A recurring NFS1 pathogenic variant causes a mitochondrial disorder with variable intra-familial patient outcomes. Molecular Genetics and Metabolism Reports. 26. 100699–100699. 10 indexed citations
19.
Sagi‐Dain, Lena, Alina Kurolap, Anat Ilivitzki, et al.. (2019). A novel heterozygous loss‐of‐function DCC Netrin 1 receptor variant in prenatal agenesis of corpus callosum and review of the literature. American Journal of Medical Genetics Part A. 182(1). 205–212. 8 indexed citations
20.
Feldman, Hagit Baris. (1976). Arrangement of transfer-RNA genes in yeast. Nucleic Acids Research. 3(9). 2379–2386. 30 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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