Edwin P. Kirk

8.5k citations

104 papers · 3.2k · h-index 27

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Statistics and Probability top 2%
- Cognitive and developmental aspects of mathematical skills

Papers in

Molecular Biology 55
- Congenital heart defects research 23
- Mitochondrial Function and Pathology 9
Genetics 32
- Genomic variations and chromosomal abnormalities 14
- Genomics and Rare Diseases 10

Co-authors: Mark H. Ashcraft (2 shared papers)Richard P. Harvey (16 shared papers)David S. Winlaw (15 shared papers)Gary F. Sholler (14 shared papers)Gillian M. Blue (12 shared papers)Michael P. Feneley (5 shared papers)Diane Fatkin (4 shared papers)Michael Venning (1 shared paper)
Journals: European Journal of Human Genetics (7 papers)Prenatal Diagnosis (5 papers)Genetics in Medicine (4 papers)Journal of Medical Genetics (3 papers)European Journal of Medical Genetics (3 papers)
Partner nations: Australia United States United Kingdom

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-authors

The 25 scholars most cited alongside Edwin P. Kirk, 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 Edwin P. Kirk Line = papers co-authored together Edwin P. Kirk links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 104 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Factor H Mutations in Hemolytic Uremic Syndrome Cluster in Exons 18–20, a Domain Important for Host Cell Recognition The American Journal of Human Genetics ·Anna Richards, M. Buddles, Rosemary L. Donne, Bernard S. Kaplan, Edwin P. Kirk, Michael Venning, Christian Tielemans, Judith A. Goodship, Timothy H.J. Goodship	2001	254
2	The relationships among working memory, math anxiety, and performance. Journal of Experimental Psychology General ·Mark H. Ashcraft, Edwin P. Kirk	2001	237
3	Congenital heart disease: current knowledge about causes and inheritance The Medical Journal of Australia ·Gillian M. Blue, Edwin P. Kirk, Gary F. Sholler, Richard P. Harvey, David S. Winlaw	2012	206
4	Cardiac homeobox gene NKX2-5mutations and congenital heart disease Journal of the American College of Cardiology ·David A. Elliott, Edwin P. Kirk, Thomas Yeoh, Suchitra Chandar, Fiona McKenzie, Peter Taylor, Paul Grossfeld, Diane Fatkin, Owen D. Jones, Peter Hayes, Michael P. Feneley, Richard P. Harvey	2003	183
5	NDUFS6 mutations are a novel cause of lethal neonatal mitochondrial complex I deficiency 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	2004	163
6	Telling stories: The perils and promise of using verbal reports to study math strategies. Journal of Experimental Psychology Learning Memory and Cognition ·Edwin P. Kirk, Mark H. Ashcraft	2001	141
7	Expanded Newborn Screening: Outcome in Screened and Unscreened Patients at Age 6 Years PEDIATRICS ·Bridget Wilcken, Marion Haas, Pamela Joy, Veronica Wiley, Francis Bowling, Kevin Carpenter, John Christodoulou, David Cowley, Carolyn Ellaway, Janice M. Fletcher, Edwin P. Kirk, Barry Lewis, Jim McGill, Heidi Peters, James Pitt, Enzo Ranieri, Joy Yaplito‐Lee, Avihu Boneh	2009	127
8	α-Cardiac myosin heavy chain (MYH6) mutations affecting myofibril formation are associated with congenital heart defects Human Molecular Genetics ·Javier T Granados-Riveron, Tushar K. Ghosh, Mark Pope, Frances Bu’Lock, Christopher Thornborough, Jacqueline Eason, Edwin P. Kirk, Diane Fatkin, Michael P. Feneley, Richard P. Harvey, John A.L. Armour, J. David Brook	2010	115
9	Twenty-two novel mutations in the lysosomal ?-glucosidase gene (GAA) underscore the genotype-phenotype correlation in glycogen storage disease type II Human Mutation ·M M Hermans, Dik van Leenen, Marian A. Kroos, Clare Beesley, Ans T. van der Ploeg, Hitoshi Sakuraba, Ron A. Wevers, Wim Kleijer, Helen Michelakakis, Edwin P. Kirk, Janice M. Fletcher, N. U. Bosshard, Lina Basel‐Vanagaite, G. T. N. Besley, Arnold Reuser	2003	113
10	Advances in the Genetics of Congenital Heart Disease Journal of the American College of Cardiology ·Gillian M. Blue, Edwin P. Kirk, Eleni Giannoulatou, Gary F. Sholler, Sally L. Dunwoodie, Richard P. Harvey, David S. Winlaw	2017	106
11	Rapamycin treatment for a child with germline PTEN mutation Nature Clinical Practice Oncology ·Deborah J. Marsh, Toby N. Trahair, Janet L. Martin, Wey Yeeng Chee, Jan L Walker, Edwin P. Kirk, Robert C. Baxter, Glenn M. Marshall	2008	100
12	Mutations in LYRM4, encoding iron–sulfur cluster biogenesis factor ISD11, cause deficiency of multiple respiratory chain complexes Human Molecular Genetics ·Sze Chern Lim, Martin Friemel, Justine E. Marum, Elena J. Tucker, Damien L. Bruno, Lisa G. Riley, John Christodoulou, Edwin P. Kirk, Avihu Boneh, Christine M. DeGennaro, Michael Springer, Vamsi K. Mootha, Tracey A. Rouault, Silke Leimkühler, David R. Thorburn, Alison G. Compton	2013	81
13	Combined Mutation Screening of NKX2-5, GATA4, and TBX5 in Congenital Heart Disease: Multiple Heterozygosity and Novel Mutations Congenital Heart Disease ·Javier T Granados-Riveron, Mark Pope, Frances Bu’Lock, Christopher Thornborough, Jacqueline Eason, Kerry Setchfield, Ami Ketley, Edwin P. Kirk, Diane Fatkin, Michael P. Feneley, Richard P. Harvey, J. David Brook	2011	71
14	Targeted Next-Generation Sequencing Identifies Pathogenic Variants in Familial Congenital Heart Disease Journal of the American College of Cardiology ·Gillian M. Blue, Edwin P. Kirk, Eleni Giannoulatou, Sally L. Dunwoodie, Joshua W. K. Ho, Desiree Hilton, Susan M. White, Gary F. Sholler, Richard P. Harvey, David S. Winlaw	2014	63
15	International perspectives on the implementation of reproductive carrier screening Prenatal Diagnosis ·Martin B. Delatycki, Fowzan S. Alkuraya, Alison D. Archibald, Carlo Castellani, Martina C. Cornel, Wayne W. Grody, Lidewij Henneman, Adonis S. Ioannides, Edwin P. Kirk, Nigel G. Laing, Anneke Lucassen, John Massie, Juliëtte Schuurmans, Meow‐Keong Thong, Irene M. van Langen, Joël Zlotogora	2019	61
16	Mutations in the gene encoding the PML nuclear body protein Sp110 are associated with immunodeficiency and hepatic veno-occlusive disease Nature Genetics ·Tony Roscioli, Simon T. Cliffe, Donald B. Bloch, Christopher G. Bell, Glenda Mullan, Peter J. Taylor, Maria Sarris, Joanne Wang, Jennifer A. Donald, Edwin P. Kirk, John B. Ziegler, Ulrich Salzer, George B. McDonald, Melanie Wong, Robert W. Lindeman, Michael F. Buckley	2006	60
17	Homeodomain Factor Nkx2-5 in Heart Development and Disease Cold Spring Harbor Symposia on Quantitative Biology ·Richard P. Harvey, D. Lai, David A. Elliott, Christine Biben, Mark J. Solloway, Owen W.J. Prall, Fiona A. Stennard, Aaron Schindeler, Nicola Groves, Lopeti T. Lavulo, Changbaig Hyun, Thomas Yeoh, Mauro W. Costa, Milena B. Furtado, Edwin P. Kirk	2002	55
18	Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype American Journal of Medical Genetics Part A ·Ingrid Scurr, Louise C. Wilson, Melissa Lees, Stephen P. Robertson, Edwin P. Kirk, Anne Turner, John Morton, Alexa Kidd, Vandana Shashi, Christy Stanley, Margaret N. Berry, Alan D. Irvine, David Goudie, Claire Turner, Carole Brewer, Sarah Smithson	2011	54
19	GATA4 Mutations in 357 Unrelated Patients with Congenital Heart Malformation Genetic Testing and Molecular Biomarkers ·Tanya L. Butler, Giorgia Esposito, Gillian M. Blue, Andrew D. Cole, Mauro W. Costa, Leigh B. Waddell, Gina Walizada, Gary F. Sholler, Edwin P. Kirk, Michael P. Feneley, Richard P. Harvey, David S. Winlaw	2010	48
20	Cantú syndrome: Findings from 74 patients in the International Cantú Syndrome Registry American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Dorothy K. Grange, Helen I. Roessler, Conor McClenaghan, Karen Duran, Kathleen S. Shields, Marı́a S. Remedi, Nine Knoers, Jin‐Moo Lee, Edwin P. Kirk, Ingrid Scurr, Sarah Smithson, Gautam K. Singh, Mieke M. van Haelst, Colin G. Nichols, Gijs van Haaften	2019	44

About Edwin P. Kirk

Edwin P. Kirk is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Pulmonary and Respiratory Medicine and Epidemiology, having authored 104 papers that have together received 3.2k indexed citations. Recurring topics across this work include Congenital heart defects research (23 papers), Congenital Heart Disease Studies (17 papers), Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (14 papers), Metabolism and Genetic Disorders (14 papers), Genomics and Rare Diseases (10 papers), Mitochondrial Function and Pathology (9 papers) and Cystic Fibrosis Research Advances (9 papers). The work is most often cited by research in Clinical Biochemistry (386 citations), Statistics and Probability (216 citations), Molecular Biology (1.5k citations), Epidemiology (765 citations) and Genetics (516 citations). Edwin P. Kirk has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Mark H. Ashcraft, Richard P. Harvey, David S. Winlaw, Gary F. Sholler, Gillian M. Blue, Michael P. Feneley, Diane Fatkin, Michael Venning, M. Buddles and Sally L. Dunwoodie. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis, Genetics in Medicine, Journal of Medical Genetics and European Journal of Medical 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.

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