Patricia Birch

3.5k total citations
56 papers, 1.9k citations indexed

About

Patricia Birch is a scholar working on Neurology, Genetics and Rheumatology. According to data from OpenAlex, Patricia Birch has authored 56 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Neurology, 21 papers in Genetics and 10 papers in Rheumatology. Recurrent topics in Patricia Birch's work include Neurofibromatosis and Schwannoma Cases (21 papers), Genomics and Rare Diseases (15 papers) and BRCA gene mutations in cancer (15 papers). Patricia Birch is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (21 papers), Genomics and Rare Diseases (15 papers) and BRCA gene mutations in cancer (15 papers). Patricia Birch collaborates with scholars based in Canada, United States and Germany. Patricia Birch's co-authors include Jan M. Friedman, Shelin Adam, Anne Townsend, P. Wolkenstein, François Rousseau, Minna Pöyhönen, Vincent M. Riccardi, Jacek Szudek, Carlo A. Marra and Bruce R. Korf and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and American Journal of Obstetrics and Gynecology.

In The Last Decade

Patricia Birch

54 papers receiving 1.8k citations

Peers

Patricia Birch

NEURO

GENET

RHEUM

EPIDE

Bonnie Jeanne Baty United States

V Blair United Kingdom

Patrick Dhellemmes France

Eyal Muscal United States

Caroline Benjamin United Kingdom

Ignacio Blanco Spain

Howard P. Levy United States

Dawn H. Siegel United States

Saskia M. Imhof Netherlands

Rita Mingarelli Italy

Bonnie Jeanne Baty United States

Patricia Birch

418 ×0.5

NEURO

1.3k ×2.0

GENET

148 ×0.4

RHEUM

250 ×0.7

EPIDE

319 ×1.2

Citations per year, relative to Patricia Birch Patricia Birch (= 1×) peers Bonnie Jeanne Baty

Countries citing papers authored by Patricia Birch

Since Specialization

Citations

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

Fields of papers citing papers by Patricia Birch

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patricia Birch

This figure shows the co-authorship network connecting the top 25 collaborators of Patricia Birch. A scholar is included among the top collaborators of Patricia Birch 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 Patricia Birch. Patricia Birch 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

Elliott, Alison M., Jehannine Austin, Bartha Maria Knoppers, et al.. (2025). The impact of genetic counselor involvement in genetic and genomic test order review: A scoping review. Genetics in Medicine. 27(3). 101354–101354. 2 indexed citations

Birch, Patricia, Cyrus Boelman, Mary Connolly, et al.. (2024). Where there is no genetic counselor: An online decision-aid supports the majority of parents’ diagnostic genomic testing choices for their children. Genetics in Medicine. 26(9). 101173–101173. 1 indexed citations

Macfadyen, Leah P., Jehannine Austin, Ping Cao, et al.. (2023). A novel online genomic counseling and variant interpretation certificate: Learning design, learning analytics, and evaluation. Journal of Genetic Counseling. 32(6). 1280–1287. 1 indexed citations

Birch, Patricia, et al.. (2023). Genetic counselling resources in non-english languages: A scoping review. SHILAP Revista de lepidopterología. 2. 100135–100135. 4 indexed citations

Guimond, Colleen, et al.. (2022). A personalized genomic results e-booklet, co-designed and pilot-tested by families. SHILAP Revista de lepidopterología. 1. 100039–100039. 8 indexed citations

Morris, Emily, Bartha Maria Knoppers, Larry D. Lynd, et al.. (2022). The stepwise process of integrating a genetic counsellor into primary care. European Journal of Human Genetics. 30(7). 772–781. 24 indexed citations

Dragojlovic, Nick, Ursula Ellis, Patricia Birch, et al.. (2020). The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review. Genetics in Medicine. 22(9). 1437–1449. 83 indexed citations

Ellis, Ursula, Patricia Birch, Shelin Adam, et al.. (2020). Correction: The composition and capacity of the clinical genetics workforce in high-income countries: a scoping review. Genetics in Medicine. 22(9). 1570–1570. 2 indexed citations

Karnebeek, Clara van, Ellen Kim, Patricia Birch, et al.. (2019). The cost trajectory of the diagnostic care pathway for children with suspected genetic disorders. Genetics in Medicine. 22(2). 292–300. 34 indexed citations

10.

Farschtschi, Said, Marco Marangoni, Manraj K.S. Heran, et al.. (2017). Non-optic glioma in adults and children with neurofibromatosis 1. Orphanet Journal of Rare Diseases. 12(1). 34–34. 34 indexed citations

11.

Adam, Shelin, et al.. (2016). Comparing the ability of OPTION12 and OPTION5 to assess shared decision-making in genetic counselling.. Patient Education and Counseling. 99(10). 1717–1723. 19 indexed citations

12.

Jett, Kimberly, Rosa Nguyen, Patricia Birch, et al.. (2015). Quantitative associations of scalp and body subcutaneous neurofibromas with internal plexiform tumors in neurofibromatosis 1. American Journal of Medical Genetics Part A. 167(7). 1518–1524. 5 indexed citations

13.

Karnebeek, Clara van, et al.. (2015). Costs of caring for children with an intellectual developmental disorder. Disability and health journal. 8(4). 646–651. 38 indexed citations

14.

Armstrong, Linlea, Kimberly Jett, Patricia Birch, et al.. (2013). The generalized bone phenotype in children with neurofibromatosis 1: A sibling matched case–control study. American Journal of Medical Genetics Part A. 161(7). 1654–1661. 22 indexed citations

15.

Birch, Patricia & Jan M. Friedman. (2004). Utility and limitations of genetic disease databases in clinical genetics research: A neurofibromatosis 1 database example. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 125C(1). 42–49. 6 indexed citations

16.

Khosrotehrani, Kiarash, Sylvie Bastuji‐Garin, Vincent M. Riccardi, et al.. (2004). Subcutaneous neurofibromas are associated with mortality in neurofibromatosis 1: A cohort study of 703 patients. American Journal of Medical Genetics Part A. 132A(1). 49–53. 47 indexed citations

17.

Kwok, Edmund, Bonita Sawatzky, Patricia Birch, Jan M. Friedman, & Stephen J. Tredwell. (2002). Vertebral scalloping in neurofibromatosis type 1: a quantitative approach.. Europe PMC (PubMed Central). 45(3). 181–4. 6 indexed citations

18.

Stevenson, David A., Patricia Birch, Jan M. Friedman, et al.. (1999). Descriptive analysis of tibial pseudarthrosis in patients with neurofibromatosis 1. American Journal of Medical Genetics. 84(5). 413–419. 96 indexed citations

19.

Friedman, Jan M. & Patricia Birch. (1997). An Association Between Optic Glioma and Other Tumours of the Central Nervous System in Neurofibromatosis Type 1. Neuropediatrics. 28(2). 131–132. 29 indexed citations

20.

Friedman, Jan M., et al.. (1993). National Neurofibromatosis Foundation International Database. American Journal of Medical Genetics. 45(1). 88–91. 33 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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