Jo-Anne Herbrick

1.8k total citations
17 papers, 855 citations indexed

About

Jo-Anne Herbrick is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Jo-Anne Herbrick has authored 17 papers receiving a total of 855 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Immunology. Recurrent topics in Jo-Anne Herbrick's work include Immunodeficiency and Autoimmune Disorders (4 papers), RNA modifications and cancer (3 papers) and Congenital Diaphragmatic Hernia Studies (2 papers). Jo-Anne Herbrick is often cited by papers focused on Immunodeficiency and Autoimmune Disorders (4 papers), RNA modifications and cancer (3 papers) and Congenital Diaphragmatic Hernia Studies (2 papers). Jo-Anne Herbrick collaborates with scholars based in Canada, United Kingdom and United States. Jo-Anne Herbrick's co-authors include Stephen W. Scherer, Chaim M. Roifman, Nigel Sharfe, Jeremy A. Squire, Harjit Dadi, Bo Ngan, Patrick Bolton, John B. Vincent, L.‐C. Tsui and Hugh Gurling and has published in prestigious journals such as Nature Genetics, Biochemical and Biophysical Research Communications and Journal of Allergy and Clinical Immunology.

In The Last Decade

Jo-Anne Herbrick

16 papers receiving 829 citations

Peers

Jo-Anne Herbrick
Laurence Delacroix Belgium
Sumita Danda India
Jackie Sheng United States
Shamir Zenvirt Israel
Silvestre Oltra Spain
Shira Rockowitz United States
Susan Kupka Germany
Mirjam W.J. Luijendijk Netherlands
Magdalena Beneyto Spain
Andrea M. Oza United States
Laurence Delacroix Belgium
Jo-Anne Herbrick
Citations per year, relative to Jo-Anne Herbrick Jo-Anne Herbrick (= 1×) peers Laurence Delacroix

Countries citing papers authored by Jo-Anne Herbrick

Since Specialization
Citations

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

Fields of papers citing papers by Jo-Anne Herbrick

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jo-Anne Herbrick. 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 Jo-Anne Herbrick. The network helps show where Jo-Anne Herbrick may publish in the future.

Co-authorship network of co-authors of Jo-Anne Herbrick

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

All Works

17 of 17 papers shown
1.
Sharfe, Nigel, Harjit Dadi, Daniele Merico, et al.. (2017). Dual loss of p110δ PI3-kinase and SKAP (KNSTRN) expression leads to combined immunodeficiency and multisystem syndromic features. Journal of Allergy and Clinical Immunology. 142(2). 618–629. 24 indexed citations
2.
Sharfe, Nigel, Daniele Merico, Harjit Dadi, et al.. (2015). The effects of RelB deficiency on lymphocyte development and function. Journal of Autoimmunity. 65. 90–100. 63 indexed citations
3.
Merico, Daniele, Nigel Sharfe, Pingzhao Hu, Jo-Anne Herbrick, & Chaim M. Roifman. (2015). RelB deficiency causes combined immunodeficiency. 2(3). 147–155. 19 indexed citations
4.
5.
Sharfe, Nigel, Amit Nahum, Harjit Dadi, et al.. (2013). Fatal combined immunodeficiency associated with heterozygous mutation in STAT1. Journal of Allergy and Clinical Immunology. 133(3). 807–817. 61 indexed citations
6.
Nakabayashi, Kazuhiko, Bridget A. Fernandez, Ikuko Teshima, et al.. (2002). Molecular Genetic Studies of Human Chromosome 7 in Russell–Silver Syndrome. Genomics. 79(2). 186–196. 25 indexed citations
7.
Ma, Zhigui, Stephan W. Morris, Virginia Valentine, et al.. (2001). Fusion of two novel genes, RBM15 and MKL1, in the t(1;22)(p13;q13) of acute megakaryoblastic leukemia. Nature Genetics. 28(3). 220–221. 210 indexed citations
8.
Vincent, John B., Jo-Anne Herbrick, Hugh Gurling, et al.. (2000). Identification of a Novel Gene on Chromosome 7q31 That Is Interrupted by a Translocation Breakpoint in an Autistic Individual. The American Journal of Human Genetics. 67(2). 510–514. 90 indexed citations
9.
Vincent, John B., Jo-Anne Herbrick, Péter Szatmári, et al.. (2000). IDENTIFICATION AND CHARACTERIZATION OF GENES SPANNING TRANSLOCATION BREAKPOINTS ON CHROMOSOME 7q31 IN TWO PATIENTS WITH AUTISTIC DISORDER. Biochemical Society Transactions. 28(5). A303–A303. 1 indexed citations
10.
Beatty, Barbara, Małgorzata Pieńkowska, Jo-Anne Herbrick, et al.. (1999). Chromosomal Localization of Phospholipase A2 Activating Protein, an Ets2 Target Gene, to 9p21. Genomics. 62(3). 529–532. 12 indexed citations
11.
12.
White, Jay A., Barbara Beckett, Stephen W. Scherer, Jo-Anne Herbrick, & Martin Petkovich. (1998). P450RAI (CYP26A1) Maps to Human Chromosome 10q23–q24 and Mouse Chromosome 19C2-3. Genomics. 48(2). 270–272. 15 indexed citations
13.
Luo, Liu‐Ying, Jo-Anne Herbrick, Stephen W. Scherer, et al.. (1998). Structural Characterization and Mapping of the Normal Epithelial Cell-Specific 1 Gene. Biochemical and Biophysical Research Communications. 247(3). 580–586. 50 indexed citations
14.
Coyle, Beth, William Reardon, Jo-Anne Herbrick, et al.. (1998). Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre). Human Molecular Genetics. 7(7). 1105–1112. 180 indexed citations
15.
Egan, Sean E., Jo-Anne Herbrick, Lap‐Chee Tsui, et al.. (1998). Mapping of the Human Lunatic Fringe (LFNG) Gene to 7p22 and Manic Fringe (MFNG) to 22q12. Genomics. 54(3). 576–577. 3 indexed citations
16.
Mansour, Sam J., Jo-Anne Herbrick, Stephen W. Scherer, & Paul Melançon. (1998). HumanGBF1Is a Ubiquitously Expressed Gene of the Sec7 Domain Family Mapping to 10q24. Genomics. 54(2). 323–327. 20 indexed citations
17.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Laurence Delacroix Breakdown of academic impact, for papers by Sumita Danda Breakdown of academic impact, for papers by Jackie Sheng Breakdown of academic impact, for papers by Shamir Zenvirt Breakdown of academic impact, for papers by Silvestre Oltra Breakdown of academic impact, for papers by Shira Rockowitz Breakdown of academic impact, for papers by Susan Kupka Breakdown of academic impact, for papers by Mirjam W.J. Luijendijk Breakdown of academic impact, for papers by Magdalena Beneyto Breakdown of academic impact, for papers by Andrea M. Oza
Rankless by CCL
2026