Steve Jeffery

10.4k citations

94 papers · 6.5k · 3 hit papers · h-index 37

Impact in

Oncology top 1%
- Lymphatic System and Diseases
Cardiology and Cardiovascular Medicine top 1%
- Cardiovascular Effects of Exercise
- Cardiac electrophysiology and arrhythmias
- Cardiomyopathy and Myosin Studies

Papers in

Molecular Biology 33
- Protein Tyrosine Phosphatases 10
- RNA modifications and cancer 10
Oncology 25
- Lymphatic System and Diseases 25

Co-authors: Andrew H. Crosby (10 shared papers)Kamini Kalidas (13 shared papers)Michael A. Patton (12 shared papers)Glen Brice (20 shared papers)Peter Mortimer (23 shared papers)Pia Østergaard (20 shared papers)Sahar Mansour (23 shared papers)Marco Tartaglia (5 shared papers)
Journals: Human Genetics (8 papers)Journal of Medical Genetics (7 papers)Clinical Genetics (6 papers)The American Journal of Human Genetics (4 papers)Nature Genetics (4 papers)
Partner nations: United Kingdom United States Netherlands

In The Last Decade

Steve Jeffery

93 papers receiving 6.3k citations

Steve Jeffery's Hit Papers

align trajectories log scale

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity 2002 · 528 citations

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if any of the following hold:

it has ≥500 total citations;
it reaches ≥1.5× the top-1% citation threshold for papers in the same subfield and year (the threshold is the minimum needed to enter the top 1%, not the average within it);
it reaches the top citation threshold in at least one of its specific research topics.

2002 The American Journal of Human Genetics
2001 Nature Genetics
2000 The Lancet

Peers

Countries citing papers authored by Steve Jeffery

Since Specialization

Citations

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

Fields of papers citing papers by Steve Jeffery

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Steve Jeffery, 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 Steve Jeffery Line = papers co-authored together Steve Jeffery 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 94 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome Nature Genetics ·Marco Tartaglia, Ernest L. Mehler, Rosalie Goldberg, Giuseppe Zampino, Han G. Brunner, Hannie Kremer, Ineke van der Burgt, Andrew H. Crosby, Andra Ion, Steve Jeffery, Kamini Kalidas, Michael A. Patton, Raju Kucherlapati, Bruce D. Gelb Hit paper breakdown →	2001	1198
2	Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease) The Lancet ·Godfrina McKoy, Nikos Protonotarios, Andrew H. Crosby, Adalena Tsatsopoulou, Aris Anastasakis, Aman S. Coonar, Mark Norman, C. Baboonian, Steve Jeffery, William J. McKenna Hit paper breakdown →	2000	752
3	PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity The American Journal of Human Genetics ·Marco Tartaglia, Kamini Kalidas, Adam Shaw, Xiaoling Song, Dan L. Musat, Ineke van der Burgt, Han G. Brunner, Débora Romeo Bertola, Andrew H. Crosby, Andra Ion, Raju Kucherlapati, Steve Jeffery, Michael A. Patton, Bruce D. Gelb Hit paper breakdown →	2002	528
4	Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome) Nature Genetics ·Pia Østergaard, Michael A. Simpson, Fiona Connell, Colin G. Steward, Glen Brice, Wesley J. Woollard, Dimitra Dafou, Tatjana Kilo, Sarah Smithson, Peter Lunt, Victoria A. Murday, Shirley Hodgson, Russell Keenan, Daniela T. Pilz, Inés Martínez‐Corral, Taija Mäkinen, Peter Mortimer, Steve Jeffery, Richard C. Trembath, Sahar Mansour	2011	350
5	Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families European Heart Journal ·Elijah R. Behr, Chrysoula Dalageorgou, Michael Christiansen, Petros Syrris, Siân Hughes, Maite Tome, Edward Rowland, Steve Jeffery, William J. McKenna	2008	294
6	Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalis Nature Communications ·Elisavet Fotiou, Silvia Martin‐Almedina, Michael A. Simpson, Shin Lin, Kristiana Gordon, Glen Brice, Giles Atton, Iona Jeffery, David C. Rees, Cyril Mignot, Julie Vogt, Tessa Homfray, M Snyder, Stanley G. Rockson, Steve Jeffery, Peter Mortimer, Sahar Mansour, Pia Østergaard	2015	226
7	Lipedema: An inherited condition American Journal of Medical Genetics Part A ·Anne H. Child, Kristiana Gordon, Pip Sharpe, Glen Brice, Pia Østergaard, Steve Jeffery, Peter Mortimer	2010	194
8	Mapping a gene for Noonan syndrome to the long arm of chromosome 12 Nature Genetics ·C. Ruth Jamieson, Ineke van der Burgt, Angela F. Brady, Margo van Reen, Madiha M. Elsawi, Frans A. Hol, Steve Jeffery, Michael A. Patton, Edwin C.M. Mariman	1994	188
9	Mutations in FOXC2 Are Strongly Associated With Primary Valve Failure in Veins of the Lower Limb Circulation ·Russell H. Mellor, Glen Brice, A.W.B. Stanton, Jane O. French, Alberto Smith, Steve Jeffery, J. R. Levick, K G Burnand, Peter Mortimer	2007	141
10	Mutation in Vascular Endothelial Growth Factor-C, a Ligand for Vascular Endothelial Growth Factor Receptor-3, Is Associated With Autosomal Dominant Milroy-Like Primary Lymphedema Circulation Research ·Kristiana Gordon, Dörte Schulte, Glen Brice, Michael A. Simpson, M. Guy Roukens, Andreas van Impel, Fiona Connell, Kamini Kalidas, Steve Jeffery, Peter Mortimer, Sahar Mansour, Stefan Schulte‐Merker, Pia Østergaard	2013	126
11	Transforming growth factor-β1 gene polymorphisms and coronary artery disease Clinical Science ·Petros Syrris, Nicholas D. Carter, James C. Metcalfe, Paul R. Kemp, David J. Grainger, Juan Carlos Kaski, David C. Crossman, Sheila Francis, Julian Gunn, Steve Jeffery, Kirsten Heathcote	1998	125
12	The classification and diagnostic algorithm for primary lymphatic dysplasia: an update from 2010 to include molecular findings Clinical Genetics ·FC Connell, Kristiana Gordon, Glen Brice, Vaughan Keeley, Steve Jeffery, P.S. Mortimer, Sahar Mansour, Pia Østergaard	2013	105
13	Analysis of lymphoedema-distichiasis families forFOXC2 mutations reveals small insertions and deletions throughout the gene Human Genetics ·Rachel E. Bell, Glen Brice, Anne H. Child, V Murday, Sahar Mansour, C. Sandy, J R O Collin, Angela F. Brady, David F. Callen, K G Burnand, Peter Mortimer, Steve Jeffery	2001	96
14	Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype Journal of Medical Genetics ·Pia Østergaard, Michael A. Simpson, Glen Brice, Sahar Mansour, Fiona Connell, Alexandros Onoufriadis, A. H. Child, (unknown), Kamini Kalidas, Peter Mortimer, Richard C. Trembath, Steve Jeffery	2011	86
15	Angiotensin converting enzyme gene I/D polymorphism, blood pressure and the renin-angiotensin system in Caucasian and Afro-Caribbean peoples. PubMed ·Jacqueline Barley, A Blackwood, Michelle A. Miller, Nirmala D. Markandu, Nicholas D. Carter, Steve Jeffery, Francesco P. Cappuccio, Graham A. MacGregor, Giuseppe A. Sagnella	1996	80
16	Common Variation in the NOS1AP Gene Is Associated With Drug-Induced QT Prolongation and Ventricular Arrhythmia Journal of the American College of Cardiology ·Yalda Jamshidi, Ilja M. Nolte, Chrysoula Dalageorgou, Dongling Zheng, Toby Johnson, Rachel Bastiaenen, Suzanne Ruddy, Daniel Talbott, Kris Norris, Harold Snieder, Alfred L. George, Vanessa Marshall, Saad Shakir, Prince J. Kannankeril, Patricia B. Munroe, A. John Camm, Steve Jeffery, Dan M. Roden, Elijah R. Behr	2012	77
17	Angiotensin-Converting Enzyme Gene Polymorphism Circulation ·Donald R.J. Singer, Constantinos G. Missouris, Steve Jeffery	1996	73
18	One gene, two phenotypes:ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B Human Mutation ·Ali R. Afzal, Steve Jeffery	2003	72
19	Evolution of Protein Molecules Biochemical Society Transactions ·Steve Jeffery	1979	72
20	Association of interleukin-6 -174G/C promoter polymorphism with hypertension and left ventricular hypertrophy in dialysis patients Kidney International ·Attilio Losito, Kamini Kalidas, Stefania Santoni, Steve Jeffery	2003	70

About Steve Jeffery

Steve Jeffery is a scholar working on Molecular Biology, Oncology, Surgery, Genetics and Cardiology and Cardiovascular Medicine, having authored 94 papers that have together received 6.5k indexed citations. Recurring topics across this work include Lymphatic System and Diseases (25 papers), Protein Tyrosine Phosphatases (10 papers), RNA modifications and cancer (10 papers), Galectins and Cancer Biology (8 papers), Genetic and Kidney Cyst Diseases (8 papers), Vascular Malformations and Hemangiomas (8 papers), Skin and Cellular Biology Research (7 papers) and Cardiac electrophysiology and arrhythmias (6 papers). The work is most often cited by research in Oncology (1.6k citations), Cardiology and Cardiovascular Medicine (1.2k citations), Immunology (1.1k citations), Molecular Biology (3.1k citations) and Cell Biology (587 citations). Steve Jeffery has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Andrew H. Crosby, Kamini Kalidas, Michael A. Patton, Glen Brice, Peter Mortimer, Pia Østergaard, Sahar Mansour, Marco Tartaglia, Bruce D. Gelb and Raju Kucherlapati. Their work appears in journals such as Human Genetics, Journal of Medical Genetics, Clinical Genetics, The American Journal of Human Genetics and Nature 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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Steve Jeffery

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In The Last Decade

Steve Jeffery

Steve Jeffery's Hit Papers

Peers

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Fields of papers citing papers by Steve Jeffery

All Works

About Steve Jeffery

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