Paul A. James

26.2k citations

254 papers · 10.8k indexed · 1 hit paper · h-index 38

Impact in

Family Practice top 0.2%
Geriatrics and Gerontology top 0.2%
- Pharmaceutical Practices and Patient Outcomes

Papers in

Family Practice 13
Geriatrics and Gerontology 16

Co-authors: Barry L. Carter Eduardo Ortíz Michael Lefevre Raymond R. Townsend Suzanne Oparil Thomas D. MacKenzie Sandra J. Taler Daniel T. Lackland
Journals: Genetics in Medicine (16 papers)Human Mutation (10 papers)Familial Cancer (6 papers)Academic Medicine (5 papers)The Annals of Family Medicine (4 papers)
Partner nations: Australia United States United Kingdom

In The Last Decade

Paul A. James

241 papers receiving 10.4k citations

Hit Papers

align trajectories log scale

2014 Evidence-Based Guideline for the Management of High Blood Pressure in Adults 2013 · 5.7k citations

Peers

Countries citing papers authored by Paul A. James

Since Specialization

Citations

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

Fields of papers citing papers by Paul A. James

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Paul A. James, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Paul A. James Line = papers co-authored together Paul A. James links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Assessment of candidate high-grade serous ovarian carcinoma predisposition genes through integrated germline and tumour sequencing npj Genomic Medicine ·Alina Schuckert, В.И. Шведунов, Kathleen I. Pishas, Roghayeh Ghasemi, Simone McInerny, Simone M. Rowley, Prue E. Allan, Lisa Devereux, Dane Cheasley, Paul A. James, Ian Campbell	2025	0
2	The development and evaluation of polygenic risk score reports: A systematized review of the literature Genetics in Medicine ·ZE. Mousavi, Christian Hermelingmeier, 温兰萍, Sibel Saya, Paul A. James, Laura Forrest	2025	3
3	Management of individuals with heterozygous germline pathogenic variants in ATM: A clinical practice resource of the American College of Medical Genetics and Genomics (ACMG) Genetics in Medicine ·Tuya Pal, Katherine Schon, Catherine Paugam Burtz, Judith Balmañà, William D. Foulkes, Paul A. James, Susan Klugman, Alicia A. Livinski, Julie Mak, Joanne Ngeow, Nicoleta Voian, Myra Wick, Helen Hanson, Douglas R. Stewart, Marc Tischkowitz	2024	6
4	Development and evaluation of a novel educational program for providers on the use of polygenic risk scores Genetics in Medicine ·Tatiane Yanes, Baharuddin M. Ranggang, Mary‐Anne Young, Rafael Antonino Sauleo, Amanda Willis, Petter Hojem, Bronwyn Terrill, Simone McInerny, Laura Forrest, 赵坤, Rachel Williams, Marianna Masmanidou, Paul A. James	2023	4
5	Population-based BRCA1/2 testing programmes are highly acceptable in the Jewish community: results of the JeneScreen Study Journal of Medical Genetics ·Jane Tiller, Chiara Penengo, Rajneesh Kaur, Simone M. Rowley, Yi-An Ko, Jingang Li, Agnes Bankier, Bettina Meiser, Kristine Barlow‐Stewart, Leslie Burnett, Chris Jacobs, Paul A. James, Alison H. Trainer, Mark Michaud, Ian Campbell, Lesley Andrews, Martin B. Delatycki	2022	5
6	Somatic inactivation of breast cancer predisposition genes in tumors associated with pathogenic germline variants JNCI Journal of the National Cancer Institute ·Жанна Тома, Na Li, Jingang Li, Simone McInerny, Magnus Zethoven, Simone M. Rowley, Tony M. Woodward, Fiyenti Susanti, Xiaojuan Li, Mariarosaria D'Alfonso, Lisa Devereux, Rodney J. Scott, Erica K. Sloan, Paul A. James, Ian Campbell	2022	6
7	Causes, circumstances, and potential preventability of cardiac arrest in the young: insights from a state-wide clinical and forensic registry EP Europace ·E. Paratz, Shu-Wei Hsiao, Dominica Zentner, Natalie Morgan, Karen Smith, Tina Thompson, Paul A. James, V. Connell, Andreas Pflaumer, Christopher Semsarian, Jodie Ingles, Sarah Parsons, Dion Stub, André La Gerche	2022	23
8	Real world outcomes and implementation pathways of exome sequencing in an adult genetic department Genetics in Medicine ·Maie Walsh, Mr. Oleg Ye. Sysoyev, Jessica Taylor, Bryony A. Thompson, 修樫原, Adrienne Sexton, А.В. Кудряков, І.-А. В. Кондрат, Yi-jun Zhao, Sinwook Lee, Michael Fahey, Michael Christie, Ingrid Winship, Alison H. Trainer, Paul A. James	2022	4
9	Inconsistent discharge diagnoses for young cardiac arrest episodes: insights from a statewide registry Internal Medicine Journal ·E. Paratz, Shu-Wei Hsiao, Jocasta Ball, Karen Smith, Dominica Zentner, Natalie Morgan, Sarah Parsons, Tina Thompson, Paul A. James, V. Connell, Andreas Pflaumer, Christopher Semsarian, Jodie Ingles, Dion Stub, André La Gerche	2022	1
10	The economic impact of sudden cardiac arrest Resuscitation ·E. Paratz, Karen Smith, Jocasta Ball, Shu-Wei Hsiao, Dominica Zentner, Sarah Parsons, Natalie Morgan, Tina Thompson, Paul A. James, Andreas Pflaumer, Christopher Semsarian, Dion Stub, Danny Liew, André La Gerche	2021	16
11	Uptake of polygenic risk information among women at increased risk of breast cancer Clinical Genetics ·Tatiane Yanes, Bettina Meiser, Rajneesh Kaur, Bruna de Oliveira Cassettari, Simone McInerny, Mackenzie Roberts, Kristine Barlow‐Stewart, Yoland Antill, Lucinda Salmon, Luisa Veronis, Mary‐Anne Young, Paul A. James	2019	19
12	Combined Tumor Sequencing and Case-Control Analyses of RAD51C in Breast Cancer JNCI Journal of the National Cancer Institute ·Na Li, Simone McInerny, Magnus Zethoven, Dane Cheasley, Жанна Тома, Simone M. Rowley, Lisa Devereux, Manoela de Sousa Correia, Chu We, David J. Byrne, Xiaojuan Li, Jason Li, Stephen B. Fox, Thomas John, Yoland Antill, Kylie L. Gorringe, Paul A. James, Ian Campbell	2019	23
13	Improved, ACMG-compliant, in silico prediction of pathogenicity for missense substitutions encoded by TP53 variants Human Mutation ·Cristina Fortuño, Paul A. James, Erin L. Young, Bing Feng, Magali Olivier, Tina Pesaran, Sean V. Tavtigian, Amanda B. Spurdle	2018	27
14	Family Medicine Research in the United States From the late 1960s Into the Future. PubMed ·Marjorie A. Bowman, Sean C. Lucan, Thomas C. Rosenthal, Arch G. Mainous, Paul A. James	2017	31
15	A clinically driven variant prioritization framework outperforms purely computational approaches for the diagnostic analysis of singleton WES data European Journal of Human Genetics ·(unknown), Zornitza Stark, Harriet Dashnow, Sebastian Lunke, Tiong Yang Tan, Alison Yeung, Simon Sadedin, Natalie Thorne, Ivan Macciocca, Clara Gaff, Alicia Oshlack, Susan M. White, Paul A. James	2017	13
16	Cpipe: a shared variant detection pipeline designed for diagnostic settings Genome Medicine ·Simon Sadedin, Harriet Dashnow, Paul A. James, Melanie Bahlo, Denis C. Bauer, Andrew Lonie, Sebastian Lunke, Ivan Macciocca, Jason P. Ross, Kirby Siemering, Zornitza Stark, Susan M. White, (unknown), Graham R. Taylor, Clara Gaff, Alicia Oshlack, Natalie Thorne	2015	54
17	“Cancer 2015”: A Prospective, Population-Based Cancer Cohort—Phase 1: Feasibility of Genomics-Guided Precision Medicine in the Clinic Journal of Personalized Medicine ·John P. Parisot, Heather Thorne, Andrew Fellowes, Ken Doig, Mark Lucas, John J. McNeil, Brett Doble, Alexander Dobrovic, Thomas John, Paul A. James, Lara Lipton, David M. Ashley, Theresa Hayes, Paul J. McMurrick, Gary Richardson, Paula Lorgelly, Stephen B. Fox, David M. Thomas	2015	8
18	Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene Neurology ·Paul A. James, M. Zameel Cader, F. Muntoni, Anne Marie Childs, Yanick J. Crow, Kevin Talbot	2006	68
19	The ultrasound-assisted physical examination in the periodic health evaluation of the elderly. PubMed ·Cheng-Chieh Chuang, Maritza Canales, Paul A. James, John Rezk Hanna Elseberbihy	2000	17
20	Hyperbaric oxygen for patients with multiple sclerosis BMJ ·Paul A. James	1984	1

About Paul A. James

Paul A. James is a scholar working on Family Practice, Geriatrics and Gerontology, Genetics, Cancer Research and Cardiology and Cardiovascular Medicine, having authored 254 papers that have together received 10.8k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (72 papers), Cancer Genomics and Diagnostics (34 papers), Genomics and Rare Diseases (33 papers), Genetic factors in colorectal cancer (26 papers), Genomic variations and chromosomal abnormalities (20 papers), Cardiovascular Effects of Exercise (17 papers), Health Systems, Economic Evaluations, Quality of Life (16 papers) and Cardiac electrophysiology and arrhythmias (16 papers). The work is most often cited by research in Family Practice (553 citations), Geriatrics and Gerontology (912 citations), Cardiology and Cardiovascular Medicine (4.8k citations), Endocrinology, Diabetes and Metabolism (1.4k citations) and Nephrology (439 citations). Paul A. James has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Barry L. Carter, Eduardo Ortíz, Michael Lefevre, Raymond R. Townsend, Suzanne Oparil, Thomas D. MacKenzie, Sandra J. Taler, Daniel T. Lackland, Sidney C. Smith and Olugbenga Ogedegbe. Their work appears in journals such as Genetics in Medicine, Human Mutation, Familial Cancer, Academic Medicine and The Annals of Family Medicine.

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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