Bryony A. Thompson

2.8k citations

39 papers · 824 indexed · h-index 15

Co-authors: Amanda B. Spurdle Michael T. Parsons Daniel D. Buchanan Joanne Young Rolf H. Sijmons Finlay Macrae Sean V. Tavtigian Michael O. Woods
Topics: Genetic factors in colorectal cancer (22 papers)Cancer Genomics and Diagnostics (18 papers)Genomics and Rare Diseases (14 papers)
Cited by: Pathology and Forensic Medicine Cancer Research Oncology
Journals: Bioinformatics International Journal of Molecular Sciences The American Journal of Human Genetics
Partner nations: Australia United States Netherlands

In The Last Decade

Bryony A. Thompson

37 papers receiving 822 citations

Peers

Countries citing papers authored by Bryony A. Thompson

Since Specialization

Citations

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

Fields of papers citing papers by Bryony A. Thompson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Bryony A. Thompson. 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 Bryony A. Thompson. The network helps show where Bryony A. Thompson may publish in the future.

Co-authorship network of co-authors of Bryony A. Thompson

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Specifications of the ACMG/AMP Variant Curation Guidelines for Hereditary Hemorrhagic Telangiectasia Genes—ENG and ACVRL1 2024 ·Human Mutation ·(unknown),Jamie McDonald,Carmelo Bernabéu,(unknown),Carla Olivieri,(unknown),(unknown),Bryony A. Thompson,Luca Jovine,Claire L. Shovlin,Sophie Dupuis‐Girod,Gaëtan Lesca,Maud Tusseau,Arupa Ganguly,Raj S. Kasthuri,(unknown),Maarten P.G. Massink,Shoji Ichikawa,Pınar Bayrak‐Toydemir	5
2	Clinical application of whole genome sequencing in young onset dementia: challenges and opportunities 2024 ·Expert Review of Molecular Diagnostics ·Aamira Huq,Bryony A. Thompson,Ingrid Winship	1
3	Real world outcomes and implementation pathways of exome sequencing in an adult genetic department 2022 ·Genetics in Medicine ·Maie Walsh,(unknown),Jessica Taylor,Bryony A. Thompson,(unknown),Adrienne Sexton,(unknown),(unknown),(unknown),(unknown),Michael Fahey,Michael Christie,Ingrid Winship,Alison H. Trainer,Paul A. James	4
4	Comprehensive evaluation and efficient classification of BRCA1 RING domain missense substitutions 2022 ·The American Journal of Human Genetics ·Kathleen A. Clark,(unknown),Kayoko Tao,Russell Bell,(unknown),Judith Rosenthal,(unknown),(unknown),Bryony A. Thompson,(unknown),Jason Gertz,Katherine E. Varley,Kenneth M. Boucher,David E. Goldgar,William D. Foulkes,Alun Thomas,Sean V. Tavtigian	8
5	Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent 2021 ·npj Genomic Medicine ·Paul Lacaze,Robert Sebra,Moeen Riaz,Jodie Ingles,Jane Tiller,Bryony A. Thompson,Paul A. James,Diane Fatkin,Christopher Semsarian,Christopher M. Reid,Andrew Tonkin,Ingrid Winship,Eric E. Schadt,John J. McNeil	15
6	A homozygous truncating variant in GDF9 in siblings with primary ovarian insufficiency 2021 ·Journal of Assisted Reproduction and Genetics ·(unknown),Bryony A. Thompson,James Wolfe,Sarah Price,(unknown),Alison H. Trainer	6
7	Arrhythmic Phenotypes Are a Defining Feature of Dilated Cardiomyopathy-Associated SCN5A Variants: A Systematic Review 2021 ·Circulation Genomic and Precision Medicine ·Stacey Peters,Bryony A. Thompson,Mark J. Perrin,Paul A. James,Dominica Zentner,Jonathan M. Kalman,Jamie I. Vandenberg,Diane Fatkin	27
8	Two integrated and highly predictive functional analysis-based procedures for the classification of MSH6 variants in Lynch syndrome 2020 ·Genetics in Medicine ·Mark Drost,(unknown),(unknown),Scott D. Kathe,(unknown),Fabienne M.G.R. Calléja,José B.M. Zonneveld,Kenneth M. Boucher,(unknown),Bryony A. Thompson,Lene Juel Rasmussen,Marc S. Greenblatt,(unknown),Amanda B. Spurdle,Sean V. Tavtigian,Niels de Wind	16
9	Contribution of mRNA Splicing to Mismatch Repair Gene Sequence Variant Interpretation 2020 ·Frontiers in Genetics ·Bryony A. Thompson,Rhiannon Walters,Michael T. Parsons,Troy Dumenil,Mark Drost,(unknown),Noralane M. Lindor,Sean V. Tavtigian,Niels de Wind,Amanda B. Spurdle	11
10	FANCM c5791C>T stopgain mutation (rs144567652) is a familial colorectal cancer risk factor 2020 ·Molecular Genetics & Genomic Medicine ·Lisa Cannon‐Albright,Craig C. Teerlink,Jeffrey Stevens,(unknown),Bryony A. Thompson,Russell Bell,Kim Nguyễn,(unknown),Wendy Kohlmann,Deborah W. Neklason,Sean V. Tavtigian	6
11	Determining the clinical validity of hereditary colorectal cancer and polyposis susceptibility genes using the Clinical Genome Resource Clinical Validity Framework 2018 ·Genetics in Medicine ·Bryce A. Seifert,Jennifer McGlaughon,Sarah A. Jackson,Deborah Ritter,Maegan E. Roberts,Ryan J. Schmidt,Bryony A. Thompson,(unknown),(unknown),Kristy Lee,Sharon E. Plon,Kenneth Offit,Zsofia K. Stadler,Liying Zhang,Marc S. Greenblatt,Matthew J. Ferber	17
12	Pancreatic cancer as a sentinel for hereditary cancer predisposition 2018 ·BMC Cancer ·Erin L. Young,Bryony A. Thompson,Deborah W. Neklason,Matthew A. Firpo,Theresa L. Werner,Russell Bell,(unknown),Alison Fraser,Amanda Gammon,(unknown),Wendy Kohlmann,Leigh Neumayer,David E. Goldgar,Sean J. Mulvihill,Lisa Cannon‐Albright,Sean V. Tavtigian	41
13	Panel sequencing of 264 candidate susceptibility genes and segregation analysis in a cohort of non-BRCA1, non-BRCA2 breast cancer families 2017 ·Breast Cancer Research and Treatment ·(unknown),Jun Li,(unknown),Igor V. Makunin,Bryony A. Thompson,Kayoko Tao,Erin L. Young,Jacqueline Lopez,Nicola J. Camp,Sean V. Tavtigian,Esther M. John,Irene L. Andrulis,Kum Kum Khanna,David E. Goldgar,Georgia Chenevix‐Trench	5
14	Elucidating the clinical significance of two PMS2 missense variants coexisting in a family fulfilling hereditary cancer criteria 2017 ·Familial Cancer ·(unknown),Jesús Del Valle,Matilde Navarro,Bryony A. Thompson,Sílvia Iglesias,Xavier Sanjuán,María José Paúles,Natàlia Padilla,(unknown),(unknown),Àlex Teulé,Guido Plotz,Juan Cadiñanos,Xavier de la Cruz,Francesc Balaguer,Conxi Lázaro,Marta Pineda,Gabriel Capellá	3
15	Assessment of the InSiGHT Interpretation Criteria for the Clinical Classification of 24MLH1andMSH2Gene Variants 2016 ·Human Mutation ·Rossella Tricarico,(unknown),Cristina Mareni,Bryony A. Thompson,Aurélie Drouet,(unknown),(unknown),(unknown),(unknown),(unknown),Laura Papi,Maria De Angioletti,Margherita Berardi,Pascaline Gaildrat,Omar Soukarieh,Daniela Turchetti,Alexandra Martins,Amanda B. Spurdle,Minna Nyström,Maurizio Genuardi	24
16	Correlation of tumour BRAF mutations and MLH1 methylation with germline mismatch repair (MMR) gene mutation status: a literature review assessing utility of tumour features for MMR variant classification 2012 ·Journal of Medical Genetics ·Michael T. Parsons,Daniel D. Buchanan,Bryony A. Thompson,Joanne Young,Amanda B. Spurdle	215
17	A Multifactorial Likelihood Model for MMR Gene Variant Classification Incorporating Probabilities Based on Sequence Bioinformatics and Tumor Characteristics: A Report from the Colon Cancer Family Registry 2012 ·Human Mutation ·Bryony A. Thompson,David E. Goldgar,Carol Paterson,Mark Clendenning,Rhiannon Walters,Sven Arnold,Michael T. Parsons,(unknown),Steven Gallinger,Robert W. Haile,John L. Hopper,Mark A. Jenkins,Loı̈c Le Marchand,Noralane M. Lindor,Polly A. Newcomb,Stephen N. Thibodeau,(unknown),Joanne Young,Daniel D. Buchanan,Sean V. Tavtigian,Amanda B. Spurdle	56
18	Splicing and multifactorial analysis of intronic BRCA1 and BRCA2 sequence variants identifies clinically significant splicing aberrations up to 12 nucleotides from the intron/exon boundary 2011 ·Human Mutation ·Phillip J Whiley,Lucia Guidugli,Logan C. Walker,Sue Healey,Bryony A. Thompson,Sunil R. Lakhani,Leonard Da Silva,kConFab Investigators,Sean V. Tavtigian,David E. Goldgar,Melissa A. Brown,Fergus J. Couch,Amanda B. Spurdle	32
19	Use of DNA–Damaging Agents and RNA Pooling to Assess Expression Profiles Associated with BRCA1 and BRCA2 Mutation Status in Familial Breast Cancer Patients 2010 ·PLoS Genetics ·Logan C. Walker,Bryony A. Thompson,Nicola Waddell,kConFab Investigators,Sean M. Grimmond,Amanda B. Spurdle	7
20	Detection of splicing aberrations caused by BRCA1 and BRCA2 sequence variants encoding missense substitutions: implications for prediction of pathogenicity 2010 ·Human Mutation ·Logan C. Walker,Phillip J Whiley,Fergus J. Couch,Daniel J. Farrugia,Sue Healey,Diana Eccles,Feng Lin,(unknown),Sheila Goff,Bryony A. Thompson,Sunil R. Lakhani,Leonard Da Silva,Sean V. Tavtigian,David E. Goldgar,Melissa A. Brown,Amanda B. Spurdle	40

About Bryony A. Thompson

Bryony A. Thompson is a scholar working on Pathology and Forensic Medicine, Cancer Research and Genetics, having authored 39 papers that have together received 824 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (22 papers), Cancer Genomics and Diagnostics (18 papers) and Genomics and Rare Diseases (14 papers). The work is most often cited by research in Pathology and Forensic Medicine (452 citations), Cancer Research (296 citations) and Oncology (277 citations). Bryony A. Thompson has collaborated with scholars based in Australia, United States and Netherlands. Frequent co-authors include Amanda B. Spurdle, Michael T. Parsons, Daniel D. Buchanan, Joanne Young, Rolf H. Sijmons, Finlay Macrae, Sean V. Tavtigian, Michael O. Woods, Païvi Peltomäki and John‐Paul Plazzer. Their work appears in journals such as Bioinformatics, International Journal of Molecular Sciences and The American Journal of Human Genetics.

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