Steve Jeffery

10.4k citations

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

Impact in

Immunology top 2%
- Galectins and Cancer Biology
Oncology top 1%
- Lymphatic System and Diseases

Papers in

Oncology 24
- Lymphatic System and Diseases 24
Cell Biology 14
- Skin and Cellular Biology Research 9

Co-authors: Andrew H. Crosby Kamini Kalidas Michael A. Patton Glen Brice Peter Mortimer Pia Østergaard Sahar Mansour Bruce D. Gelb
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

Hit Papers

align trajectories log scale

PTPN11 Mutations in Noonan Syndrome: Molecular Spectrum, Genotype-Phenotype Correlation, and Phenotypic Heterogeneity 2002 · 522 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-authorship network

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

#	Work
1	Redefining WILD syndrome: a primary lymphatic dysplasia with congenital multisegmental lymphoedema, cutaneous lymphovascular malformation, CD4 lymphopaenia and warts Journal of Medical Genetics ·Sahar Mansour, Katherine Josephs, Pia Østergaard, Kristiana Gordon, Manuel Andrés Palomino Delgado, Julian Pearce, Steve Jeffery, Vaughan Keeley, Katie Riches, Alexander Kreuter, Ulrike Wieland, René Hägerling, Lakshmi Ratnam, Pedro Manuel Almagro Calles, Dionysios Grigoriadis, Bernard Ho, Yarissa Palma Chorres, Iwan Kristian, Peter Mortimer, Derek C. Macallan	2021	8
2	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, Paulo Estevão Tavares Cavalcanti, Landesverein vom Roten Kreuz im Königreich Sachsen, 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	76
3	Mutations in <i>FOXC2</i> in Humans (Lymphoedema Distichiasis Syndrome) Cause Lymphatic Dysfunction on Dependency Journal of Vascular Research ·Russell H. Mellor, George Ayobami Thomas, A.W.B. Stanton, Tam C Kotsimbos, Taija Mäkinen, Alberto Smith, K G Burnand, Steve Jeffery, J. R. Levick, Peter Mortimer	2011	32
4	Lymphoedema-distichiasis and FOXC2: unreported mutations, de novo mutation estimate, families without coding mutations Human Genetics ·М В Штерншис, Rachel E. Bell, Glen Brice, Sahar Mansour, Mansoor Sarfarazi, Anne H. Child, Alberto Smith, Russell H. Mellor, K G Burnand, Peter Mortimer, Steve Jeffery	2005	35
5	Predictive testing for the long QT syndrome in children and teenagers - Whose best interests are served? UCL Discovery (University College London) ·愛一郎藤長, Vicente Sánchez-Biosca, E J Ladusans, Derek T. Connelly, Petros Syrris, Steve Jeffery	2003	0
6	C(−260)→T polymorphism in the promoter of CD14 receptor gene is associated with the risk of acute coronary events in patients with angina pectoris Journal of the American College of Cardiology ·Ramón Arroyo‐Espliguero, VuQuoc Luong, F.M. Doldushin, Kamini Kalidas, Juan R. Gimeno, Della Cole, Steve Jeffery, Juan Carlos Kaski	2003	1
7	T594M Mutation of the β -Subunit of the Epithelial Sodium Channel in Ghanaian Populations from Kumasi and London and a Possible Association with Hypertension Genetic Testing ·Yating Dong, Jacob Plange‐Rhule, Seif Eldin Mudawi Gasim, Frank B. Micah, J. B. Eastwood, Carlo Pohlhausen, A K Saggar-Malik, Francesco P. Cappuccio, Steve Jeffery	2002	8
8	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, Gina Levickienė, Raju Kucherlapati, Steve Jeffery, Michael A. Patton, Bruce D. Gelb Hit paper breakdown →	2002	522
9	How double eyelashes give you swollen legs British Journal of Ophthalmology ·Steve Jeffery	2002	2
10	Homocysteine levels in men and women of different ethnic and cultural background living in England Atherosclerosis ·Francesco P. Cappuccio, Xu Zhenzhen, Ivan J. Perry, Julie Gilg, Per Magne Ueland, Helga Refsum, Giuseppe A. Sagnella, Steve Jeffery, Derek G. Cook	2002	53
11	Two Families with Blepharophimosis/Ptosis/Epicanthus Inversus Syndrome Have Mutations in the Putative Forkhead Transcription Factor FOXL2 Genetic Testing ·R. Bryan Bell, Victoria A. Murday, Michael A. Patton, Steve Jeffery	2001	20
12	Amplification of a 13.5-kb Region of the PKD1 Gene Containing the 2.5-kb Polypyrimidine Tract in Intron 21 Facilitates Mutation Detection in This Gene Genetic Testing ·Ali R. Afzal, Steve Jeffery	2001	1
13	Silver syndrome is not linked to any of the previously established autosomal dominant hereditary spastic paraplegia loci American Journal of Medical Genetics ·Harshad B. Patel, Paul Hart, Thomas T. Warner, Irving C. Allen, Liao Fe, J R Silver, Nicholas Wood, Steve Jeffery, M A Patton, Andrew H. Crosby	2001	7
14	Lack of Association of ACE /Angiotensinogen Genotype with Renal Function in Autosomal Dominant Polycystic Kidney Disease Genetic Testing ·Anand K Saggar‐Malik, Ali R. Afzal, Daoliang LI, Martin Bland, MASHUR, John B. Eastwood, Graham A. MacGregor, Steve Jeffery	2000	14
15	Novel Mutations in the Duplicated Region of the Polycystic Kidney Disease 1 ( PKD1 ) Gene Provides Supporting Evidence for Gene Conversion Genetic Testing ·Ali R. Afzal, سيف متعب عبد علي, Rohan Taylor, Michael A. Patton, Anand K Saggar‐Malik, Steve Jeffery	2000	10
16	QT interval in twins Journal of Human Hypertension ·夏希八木, Harold Snieder, Steve Jeffery, Richard C. Saumarez, C. Varma, L Antoniades, TD Spector	2000	22
17	Clinical and molecular findings in a patient with a deletion on the long arm of chromosome 12. PubMed Central ·Sharon J. Hudson, Baptiste Lecoeur, Deborah L. Doherty, 生涯学習審議会社会教育分科審議会, Steve Jeffery, Шилакин Виктор Борисович, L Baljinnjam, Skye Zlotkowski	1999	17
18	Methylenetetrahydrofolate reductase polymorphism (C-677T) and coronary artery disease. PubMed ·N. M. Malik, Petros Syrris, Linor Jones, Juan Carlos Kaski, David C. Crossman, Sheila Francis, Carlo Pohlhausen, Steve Jeffery	1998	9
19	Apparent normalisation of fetal renal size in autosomal dominant polycystic kidney disease (PKD1) Clinical Genetics ·Steve Jeffery, Anand K Saggar‐Malik, Demetrios L. Economides, F da Cruz Luciano, Kay MacDermot	1998	8
20	Thrombotic thrombocytopenic purpura in a patient with genetic haemochromatosis, liver cirrhosis and an iron‐free focus British Journal of Haematology ·Sally Killick, Steve Jeffery, Hao Lin Han, Juan Pablo Quinonez Weston, Yan Ting-l	1997	1

About Steve Jeffery

Steve Jeffery is a scholar working on Oncology, Cell Biology, Cardiology and Cardiovascular Medicine, Genetics and Molecular Biology, having authored 94 papers that have together received 6.5k indexed citations. Recurring topics across this work include Lymphatic System and Diseases (24 papers), Protein Tyrosine Phosphatases (10 papers), RNA modifications and cancer (10 papers), Skin and Cellular Biology Research (9 papers), Vascular Malformations and Hemangiomas (9 papers), Genetic and Kidney Cyst Diseases (8 papers), Galectins and Cancer Biology (8 papers) and Renal and related cancers (7 papers). The work is most often cited by research in Immunology (1.3k citations), Oncology (1.7k citations), Cardiology and Cardiovascular Medicine (1.4k citations), Molecular Biology (3.3k citations) and Cell Biology (668 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, Bruce D. Gelb, Marco Tartaglia and Han G. Brunner. 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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