Jamie Allen

12.3k total citations
13 papers, 162 citations indexed

About

Jamie Allen is a scholar working on Genetics, Molecular Biology and Cancer Research. According to data from OpenAlex, Jamie Allen has authored 13 papers receiving a total of 162 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Cancer Research. Recurrent topics in Jamie Allen's work include BRCA gene mutations in cancer (6 papers), Genetic Associations and Epidemiology (4 papers) and Cancer Genomics and Diagnostics (4 papers). Jamie Allen is often cited by papers focused on BRCA gene mutations in cancer (6 papers), Genetic Associations and Epidemiology (4 papers) and Cancer Genomics and Diagnostics (4 papers). Jamie Allen collaborates with scholars based in United Kingdom, United States and Netherlands. Jamie Allen's co-authors include Douglas F. Easton, Alison M. Dunning, Karen A. Pooley, Brennan Decker, Craig Luccarini, Paul D.P. Pharoah, Manjeet K. Bolla, Robert Luben, Qin Wang and Elaine A. Ostrander and has published in prestigious journals such as Bioinformatics, Cancer Research and Human Molecular Genetics.

In The Last Decade

Jamie Allen

13 papers receiving 162 citations

Peers

Countries citing papers authored by Jamie Allen

Since Specialization

Citations

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

Fields of papers citing papers by Jamie Allen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jamie Allen

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	SUsPECT: a pipeline for variant effect prediction based on custom long-read transcriptomes for improved clinical variant annotation 2023 ·BMC Genomics ·(unknown), Nuno Saraiva-Agostinho, (unknown), Caspar I. van der Made, Simone Kersten, (unknown), Jamie Allen, Pieter‐Jan Volders, Sarah Hunt, Alexander Hoischen, Peter A.C. ’t Hoen	1
2	Minigene‐based splicing analysis and ACMG/AMP‐based tentative classification of 56 ATM variants 2022 ·The Journal of Pathology ·Elena Bueno‐Martínez, (unknown), (unknown), (unknown), (unknown), (unknown), Jamie Allen, (unknown), Pedro Pérez‐Segura, M. Durán, Douglas F. Easton, Peter Devilee, Maaike P.G. Vreeswijk, Miguel de la Hoya, Eladio A. Velasco	10
3	RAD51D Aberrant Splicing in Breast Cancer: Identification of Splicing Regulatory Elements and Minigene-Based Evaluation of 53 DNA Variants 2021 ·Cancers ·Elena Bueno‐Martínez, (unknown), (unknown), (unknown), (unknown), Sara Carvalho, Jamie Allen, Mar Infante, Pedro Pérez‐Segura, Conxi Lázaro, Douglas F. Easton, Peter Devilee, Maaike P.G. Vreeswijk, Miguel de la Hoya, Eladio A. Velasco	12
4	Easing the burden of multi‐state genetic counseling licensure in the United States: Process, pitfalls, and possible solutions 2021 ·Journal of Genetic Counseling ·Matthew L. Tschirgi, (unknown), (unknown), Jamie Allen, (unknown)	4
5	Splicing predictions, minigene analyses, and ACMG‐AMP clinical classification of 42 germline PALB2 splice‐site variants 2021 ·The Journal of Pathology ·(unknown), Elena Bueno‐Martínez, (unknown), (unknown), (unknown), (unknown), (unknown), Sara Carvalho, Jamie Allen, (unknown), Pedro Pérez‐Segura, Leila Dorling, Douglas F. Easton, Peter Devilee, Maaike P.G. Vreeswijk, Miguel de la Hoya, Eladio A. Velasco	16
6	Comprehensive Functional Characterization and Clinical Interpretation of 20 Splice-Site Variants of the RAD51C Gene 2020 ·Cancers ·(unknown), (unknown), Elena Bueno‐Martínez, Patricia Llovet, (unknown), Marı́a J. Caloca, Pedro Pérez‐Segura, (unknown), (unknown), Sara Carvalho, Jamie Allen, Douglas F. Easton, Peter Devilee, Maaike P.G. Vreeswijk, Miguel de la Hoya, Eladio A. Velasco	13
7	Targeted Resequencing of the Coding Sequence of 38 Genes Near Breast Cancer GWAS Loci in a Large Case–Control Study 2019 ·Cancer Epidemiology Biomarkers & Prevention ·Brennan Decker, Jamie Allen, Craig Luccarini, Karen A. Pooley, Mitul Shah, Manjeet K. Bolla, Qin Wang, Shahana Ahmed, Caroline Baynes, Don Conroy, Judith Brown, Robert Luben, Elaine A. Ostrander, Paul D.P. Pharoah, Alison M. Dunning, Douglas F. Easton	7
8	Differential Burden of Rare and Common Variants on Tumor Characteristics, Survival, and Mode of Detection in Breast Cancer 2018 ·Cancer Research ·Jingmei Li, (unknown), Wei Wen, Brennan Decker, Mikael Eriksson, (unknown), (unknown), Alison M. Dunning, Jamie Allen, Craig Luccarini, Karen A. Pooley, Jacques Simard, Leila Dorling, Douglas F. Easton, Soo‐Hwang Teo, Per Hall, Kamila Czene	16
9	Use of deep whole-genome sequencing data to identify structure risk variants in breast cancer susceptibility genes 2018 ·Human Molecular Genetics ·Xingyi Guo, Jiajun Shi, Qiuyin Cai, Xiao‐Ou Shu, Jing He, Wanqing Wen, Jamie Allen, Paul D.P. Pharoah, Alison M. Dunning, David J. Hunter, Peter Kraft, Douglas F. Easton, Wei Zheng, Jirong Long	15
10	Abstract S2-03: Does BRCA status affect outcome in young breast cancer patients? Results from the prospective study of outcomes in sporadic and hereditary breast cancer (POSH) 2017 ·Cancer Research ·Diana Eccles, (unknown), Tom Maishman, William Tapper, (unknown), Susan M. Gerty, Louise Stanton, (unknown), Lorraine Durcan, Peter Simmonds, Brian S. Decker, Jamie Allen, Craig Luccarini, D Easton, Alison M. Dunning, (unknown)	3
11	VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysis 2017 ·Bioinformatics ·Audrey Lemaçon, Charles Joly Beauparlant, Penny Soucy, Jamie Allen, Douglas Easton, Peter Kraft, Jacques Simard, Arnaud Droit	1
12	Rare, protein-truncating variants in ATM, CHEK2 and PALB2, but not XRCC2, are associated with increased breast cancer risks 2017 ·Journal of Medical Genetics ·Brennan Decker, Jamie Allen, Craig Luccarini, Karen A. Pooley, Mitul Shah, Manjeet K. Bolla, Qin Wang, Shahana Ahmed, Caroline Baynes, Don Conroy, Judith Brown, Robert Luben, Elaine A. Ostrander, Paul D.P. Pharoah, Alison M. Dunning, Douglas F. Easton	62
13	Abstract 4309: Rare protein truncating and missense variants in ATM, CHEK2, PALB2, but not XRCC2, confer increased breast cancer risks 2016 ·Cancer Research ·Brennan Decker, Jamie Allen, Craig Luccarini, Karen A. Pooley, Paul D.P. Pharoah, Alison M. Dunning, Douglas F. Easton	2

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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