Karin Weiss

1.4k total citations
36 papers, 433 citations indexed

About

Karin Weiss is a scholar working on Genetics, Molecular Biology and Epidemiology. According to data from OpenAlex, Karin Weiss has authored 36 papers receiving a total of 433 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 15 papers in Molecular Biology and 5 papers in Epidemiology. Recurrent topics in Karin Weiss's work include Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Karin Weiss is often cited by papers focused on Genomics and Rare Diseases (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Karin Weiss collaborates with scholars based in Israel, United States and Australia. Karin Weiss's co-authors include Kenneth K. Kídd, I. Balazs, J.R. Kidd, Francis L. Black, Maximilian Muenke, Ellen Sidransky, Grisel Lopez, Catherine Groden, Ashley N. Gonzalez and Paul Kruszka and has published in prestigious journals such as Journal of Clinical Investigation, The American Journal of Human Genetics and Journal of Hepatology.

In The Last Decade

Karin Weiss

29 papers receiving 415 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Karin Weiss Israel 13 190 188 86 65 50 36 433
Sujatha Jagadeesh India 12 165 0.9× 178 0.9× 72 0.8× 38 0.6× 50 1.0× 39 456
Emily C. Lisi United States 13 182 1.0× 142 0.8× 123 1.4× 26 0.4× 34 0.7× 22 411
Aleksandra Jezela‐Stanek Poland 14 212 1.1× 367 2.0× 116 1.3× 54 0.8× 57 1.1× 79 653
Sharan Goobie Canada 15 281 1.5× 162 0.9× 33 0.4× 49 0.8× 77 1.5× 29 504
Eugênia Ribeiro Valadares Brazil 12 148 0.8× 149 0.8× 159 1.8× 45 0.7× 93 1.9× 38 433
Anne Gläser Germany 9 75 0.4× 212 1.1× 80 0.9× 34 0.5× 40 0.8× 15 332
Elisa Biamino Italy 13 204 1.1× 188 1.0× 40 0.5× 19 0.3× 35 0.7× 25 456
Christine Broissand France 7 130 0.7× 138 0.7× 175 2.0× 51 0.8× 82 1.6× 10 416
Ohsuke Migita Japan 14 187 1.0× 290 1.5× 140 1.6× 44 0.7× 88 1.8× 41 608
Peter Heim Germany 6 75 0.4× 141 0.8× 207 2.4× 73 1.1× 56 1.1× 7 335

Countries citing papers authored by Karin Weiss

Since Specialization
Citations

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

Fields of papers citing papers by Karin Weiss

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Karin Weiss

This figure shows the co-authorship network connecting the top 25 collaborators of Karin Weiss. A scholar is included among the top collaborators of Karin Weiss 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 Karin Weiss. Karin Weiss 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.
Pichinuk, Edward, Emily Avitan‐Hersh, Ann Saada, et al.. (2025). Using chanarin-dorfman syndrome patient fibroblasts to explore disease mechanisms and new treatment avenues. Orphanet Journal of Rare Diseases. 20(1). 195–195.
2.
Paperna, Tamar, et al.. (2025). A family with an atypical presentation of TBX3-related disorder. European Journal of Medical Genetics. 73. 104994–104994.
3.
Blich, Miry, Yaniv Zohar, Victoria Cohen‐Kaplan, et al.. (2024). Ser194Leu DSG2 mutation, associated with arrhythmogenic left ventricular cardiomyopathy and ventricular tachycardia. Pacing and Clinical Electrophysiology. 47(4). 503–510.
4.
Paperna, Tamar, et al.. (2024). Rapid exome sequencing for children with severe acute encephalopathy – A case series. European Journal of Medical Genetics. 68. 104918–104918. 1 indexed citations
5.
Tal, Galit, et al.. (2024). PDSS1 mutations-associated steroid-resistant nephrotic syndrome: case report and review of literature. Pediatric Nephrology. 40(5). 1583–1589. 1 indexed citations
6.
Paperna, Tamar, Mario García‐Domínguez, Eric S. Shinwell, et al.. (2023). Exome sequencing links the SUMO protease SENP7 with fatal arthrogryposis multiplex congenita, early respiratory failure and neutropenia. Journal of Medical Genetics. 60(11). 1133–1141. 6 indexed citations
7.
Goldberg, Yael, Hanna Segev, Itay Maza, et al.. (2023). High prevalence of MUTYH associated polyposis among minority populations in Israel, due to rare founder pathogenic variants. Digestive and Liver Disease. 55(7). 880–887.
8.
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
9.
Kassis, Imad, Karin Weiss, Galit Tal, et al.. (2021). Concomitant congenital CMV infection and inherited liver diseases. European Journal of Medical Genetics. 64(8). 104249–104249. 2 indexed citations
10.
Nguyen, Quoc Toan, et al.. (2020). Deficiency of MFSD7c results in microcephaly-associated vasculopathy in Fowler syndrome. Journal of Clinical Investigation. 130(8). 4081–4093. 16 indexed citations
11.
Reches, Adi, Karin Weiss, Lily Bazak, Hagit Baris Feldman, & Idit Maya. (2019). From phenotyping to genotyping - bioinformatics for the busy clinician. European Journal of Medical Genetics. 62(8). 103689–103689. 2 indexed citations
12.
Kruszka, Paul, Seth Berger, Karin Weiss, et al.. (2019). A CCR4-NOT Transcription Complex, Subunit 1, CNOT1, Variant Associated with Holoprosencephaly. The American Journal of Human Genetics. 104(5). 990–993. 25 indexed citations
13.
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
14.
Weiss, Karin, Paul Kruszka, Eric Levey, & Maximilian Muenke. (2018). Holoprosencephaly from conception to adulthood. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 178(2). 122–127. 15 indexed citations
15.
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
16.
Martinez, Ariel F., Yu Abe, Paul Kruszka, et al.. (2017). Human germline hedgehog pathway mutations predispose to fatty liver. Journal of Hepatology. 67(4). 809–817. 25 indexed citations
17.
Berger, Seth, Karin Weiss, Ariel F. Martinez, et al.. (2017). SIX3 deletions and incomplete penetrance in families affected by holoprosencephaly. Congenital Anomalies. 58(1). 29–32. 10 indexed citations
18.
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
19.
Weiss, Karin, Aviva Fattal‐Valevski, & Shimon Reif. (2010). How to evaluate the child presenting with an apparent life-threatening event?. PubMed. 12(3). 154–7. 12 indexed citations
20.
Kidd, J.R., Francis L. Black, Karin Weiss, I. Balazs, & Kenneth K. Kídd. (1991). Studies of three Amerindian populations using nuclear DNA polymorphisms.. PubMed. 63(6). 775–94. 86 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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