Edwin P. Kirk

8.5k total citations
104 papers, 3.2k citations indexed

About

Edwin P. Kirk is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Edwin P. Kirk has authored 104 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 55 papers in Molecular Biology, 32 papers in Genetics and 18 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Edwin P. Kirk's work include Congenital heart defects research (23 papers), Congenital Heart Disease Studies (17 papers) and Prenatal Screening and Diagnostics (14 papers). Edwin P. Kirk is often cited by papers focused on Congenital heart defects research (23 papers), Congenital Heart Disease Studies (17 papers) and Prenatal Screening and Diagnostics (14 papers). Edwin P. Kirk collaborates with scholars based in Australia, United States and United Kingdom. Edwin P. Kirk's co-authors include Mark H. Ashcraft, Richard P. Harvey, David S. Winlaw, Gary F. Sholler, Gillian M. Blue, Michael P. Feneley, Diane Fatkin, Rosemary L. Donne, Michael Venning and Judith A. Goodship and has published in prestigious journals such as New England Journal of Medicine, Journal of Clinical Investigation and Nature Genetics.

In The Last Decade

Edwin P. Kirk

100 papers receiving 3.1k citations

Peers

Countries citing papers authored by Edwin P. Kirk

Since Specialization

Citations

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

Fields of papers citing papers by Edwin P. Kirk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edwin P. Kirk. 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 Edwin P. Kirk. The network helps show where Edwin P. Kirk may publish in the future.

Co-authorship network of co-authors of Edwin P. Kirk

This figure shows the co-authorship network connecting the top 25 collaborators of Edwin P. Kirk. A scholar is included among the top collaborators of Edwin P. Kirk 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 Edwin P. Kirk. Edwin P. Kirk 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	Updated penetrance estimates for recurrent copy number variants – an improved definition and formula 2025 ·European Journal of Human Genetics ·(unknown), Tracy Dudding‐Byth, Mark Pinese, Edwin P. Kirk	0
2	Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex “No Mutations Identified” Cohort 2024 ·Molecular Genetics & Genomic Medicine ·(unknown), Adam Bournazos, (unknown), Vanessa Sarkozy, John A. Lawson, Seán Kennedy, Sandra T. Cooper, Edwin P. Kirk, David Mowat	1
3	Should genes for non‐syndromic hearing loss be included in reproductive genetic carrier screening: Views of people with a personal or family experience of deafness 2023 ·Journal of Genetic Counseling ·Lucinda Freeman, (unknown), Edwin P. Kirk, Martin B. Delatycki, Jackie Leach Scully	2
4	Quantitative trait and transcriptome analysis of genetic complexity underpinning cardiac interatrial septation in mice using an advanced intercross line 2023 ·eLife ·Mahdi Moradi Marjaneh, Edwin P. Kirk, Ralph Patrick, (unknown), David T. Humphreys, Gonzalo del Monte‐Nieto, (unknown), Vaibhao Janbandhu, Tram B. Doan, Sally L. Dunwoodie, Emily Wong, Chris Moran, I.C.A. Martin, Peter C. Thomson, Richard P. Harvey	4
5	The views of people with a lived experience of deafness and the general public regarding genetic testing for deafness in the reproductive setting: A systematic review 2022 ·Genetics in Medicine ·Lucinda Freeman, (unknown), Martin B. Delatycki, Jackie Leach Scully, Edwin P. Kirk	6
6	Economic evaluation of reproductive carrier screening for recessive genetic conditions: a systematic review 2021 ·Expert Review of Pharmacoeconomics & Outcomes Research ·(unknown), (unknown), Joshua Byrnes, Paul Scuffham, Edwin P. Kirk, Martin Downes	4
7	The expandingLARS2phenotypic spectrum: HLASA, Perrault syndrome with leukodystrophy, and mitochondrial myopathy 2020 ·Human Mutation ·Lisa G. Riley, Joëlle Rudinger‐Thirion, Magali Frugier, Meredith Wilson, Melissa Luig, Thushari I. Alahakoon, (unknown), Edwin P. Kirk, Tony Roscioli, Sebastian Lunke, Zornitza Stark, Klaas J. Wierenga, Sirish Palle, Maie Walsh, Emily Higgs, Susan Arbuckle, (unknown), Alison G. Compton, David R. Thorburn, John Christodoulou	18
8	Personal genomic screening: How best to facilitate preparedness of future clients 2019 ·European Journal of Medical Genetics ·Jane Fleming, Bronwyn Terrill, Marie Dziadek, Edwin P. Kirk, Tony Roscioli, Kristine Barlow‐Stewart	3
9	User Acceptability of Whole Exome Reproductive Carrier Testing for Consanguineous Couples in Australia 2018 ·Journal of Genetic Counseling ·(unknown), Kristine Barlow‐Stewart, Arthavan Selvanathan, Tony Roscioli, A.H. Bittles, Bettina Meiser, Lisa Worgan, Sulekha Rajagopalan, Alison Colley, Edwin P. Kirk	6
10	Late-Onset Non-HLH Presentations of Growth Arrest, Inflammatory Arachnoiditis, and Severe Infectious Mononucleosis, in Siblings with Hypomorphic Defects in UNC13D 2017 ·Frontiers in Immunology ·Paul Gray, Bella Shadur, Susan Russell, Richard Mitchell, (unknown), (unknown), Ian Andrews, Kevin Thia, Joseph A. Trapani, Edwin P. Kirk, Ilia Voskoboinik	9
11	Mutations in LYRM4, encoding iron–sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes 2013 ·Human Molecular Genetics ·Sze Chern Lim, (unknown), Justine E. Marum, Elena J. Tucker, Damien L. Bruno, Lisa G. Riley, John Christodoulou, Edwin P. Kirk, Avihu Boneh, (unknown), Michael Springer, Vamsi K. Mootha, Tracey A. Rouault, Silke Leimkühler, David R. Thorburn, Alison G. Compton	81
12	Narrowing the Critical Region for Congenital Vertical Talus in Patients With Interstitial 18q Deletions 2013 ·American Journal of Medical Genetics Part A ·Paul R. Mark, (unknown), Nathalie Coré, Alan Fryer, Edwin P. Kirk, Chad Haldeman‐Englert	7
13	Parents’ perceptions of genetics services for congenital heart disease: the role of demographic, clinical, and psychological factors in determining service attendance 2013 ·Genetics in Medicine ·Nadine A. Kasparian, (unknown), Gary F. Sholler, (unknown), (unknown), Stephen G. Cooper, (unknown), Owen D. Jones, David S. Winlaw, Edwin P. Kirk	16
14	Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations 2011 ·Congenital Heart Disease ·Javier T Granados-Riveron, Mark Pope, Frances Bu’Lock, (unknown), Jacqueline Eason, Kerry Setchfield, Ami Ketley, Edwin P. Kirk, Diane Fatkin, Michael P. Feneley, Richard P. Harvey, J. David Brook	71
15	Investigation of Association between PFO Complicated by Cryptogenic Stroke and a Common Variant of the Cardiac Transcription Factor GATA4 2011 ·PLoS ONE ·Mahdi Moradi Marjaneh, Edwin P. Kirk, Maximilian Posch, C. Özcelik, Felix Berger, Roland Hetzer, Robyn Otway, Tanya L. Butler, Gillian M. Blue, Lyn R. Griffiths, Diane Fatkin, Jeremy Martinson, David S. Winlaw, Michael P. Feneley, Richard P. Harvey	4
16	GATA4 Mutations in 357 Unrelated Patients with Congenital Heart Malformation 2010 ·Genetic Testing and Molecular Biomarkers ·Tanya L. Butler, Giorgia Esposito, Gillian M. Blue, Andrew D. Cole, Mauro W. Costa, Leigh B. Waddell, (unknown), Gary F. Sholler, Edwin P. Kirk, Michael P. Feneley, Richard P. Harvey, David S. Winlaw	48
17	NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency 2004 ·Journal of Clinical Investigation ·Denise M. Kirby, Renato Salemi, Canny Sugiana, Akira Ohtake, Lee Parry, Katrina M. Bell, Edwin P. Kirk, Avihu Boneh, Robert W. Taylor, Hans‐Henrik M. Dahl, Michael T. Ryan, David R. Thorburn	14
18	Ectopic pregnancy deaths: what should be be doing? 2004 ·Journal of Hospital Medicine ·Edwin P. Kirk, G. Condous, T. Bourne	1
19	Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Cantú syndrome 1999 ·American Journal of Medical Genetics ·Stephen P. Robertson, Edwin P. Kirk, François P. Bernier, (unknown), (unknown), Agnes Bankier	2
20	Observations on Rabies in the Sudan. 1955 ·Edwin P. Kirk, (unknown), (unknown)	1

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