William Reardon

20.0k citations

196 papers · 12.4k · 4 hit papers · h-index 54

Impact in

Sensory Systems top 0.1%
- Hearing, Cochlea, Tinnitus, Genetics
Genetics top 0.1%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Connective tissue disorders research
- Genetics and Neurodevelopmental Disorders

Papers in

Genetics 96
- Craniofacial Disorders and Treatments 28
- Cleft Lip and Palate Research 21
- Genomic variations and chromosomal abnormalities 21
- Genetics and Neurodevelopmental Disorders 18
- Connective tissue disorders research 15
Molecular Biology 92
- Congenital heart defects research 17

Co-authors: Robin M. Winter (8 shared papers)Paul Rutland (8 shared papers)Louise J. Pulleyn (8 shared papers)Sue Malcolm (5 shared papers)Richard C. Trembath (14 shared papers)Barry M. Jones (5 shared papers)R M Winter (18 shared papers)Marcus Pembrey (12 shared papers)
Journals: Journal of Medical Genetics (29 papers)The American Journal of Human Genetics (9 papers)European Journal of Human Genetics (8 papers)Nature Genetics (8 papers)Clinical Genetics (7 papers)
Partner nations: United Kingdom Ireland United States

In The Last Decade

William Reardon

194 papers receiving 11.6k citations

William Reardon's Hit Papers

align trajectories log scale

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome 1995 · 739 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.

1995 Nature Genetics
1994 Nature Genetics
1994 Nature Genetics
1992 Nature

Peers

Countries citing papers authored by William Reardon

Since Specialization

Citations

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

Fields of papers citing papers by William Reardon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside William Reardon, 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 William Reardon Line = papers co-authored together William Reardon 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 196 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome Nature Genetics ·Andrew O.M. Wilkie, Sarah F. Slaney, Michael Oldridge, Michael D. Poole, Geraldine J. Ashworth, Anthony D. Hockley, Richard Hayward, David J. David, Louise J. Pulleyn, Paul Rutland, S Malcolm, Robin M. Winter, William Reardon Hit paper breakdown →	1995	739
2	Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome Nature Genetics ·William Reardon, Robin M. Winter, Paul Rutland, Louise J. Pulleyn, Barry M. Jones, Sue Malcolm Hit paper breakdown →	1994	623
3	Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy Nature ·Helen G. Harley, J. David Brook, S.A. Rundle, Stephen Crow, William Reardon, Alan Buckler, Peter S. Harper, David E. Housman, D J Shaw Hit paper breakdown →	1992	612
4	A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome Nature Genetics ·Maximilian Muenke, Ute Schell, Andreas Hehr, Nathaniel H. Robin, H. Wolfgang Losken, Albert Schinzel, Louise J. Pulleyn, Paul Rutland, William Reardon, Sue Malcolm, Robin M. Winter Hit paper breakdown →	1994	517
5	Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes Nature Genetics ·Paul Rutland, Louise J. Pulleyn, William Reardon, M Baraitser, Richard Hayward, Barry M. Jones, Sue Malcolm, Robin M. Winter, Michael Oldridge, Sarah F. Slaney, Michael D. Poole, Andrew O.M. Wilkie	1995	375
6	Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1 Human Mutation ·Frederick S. Kaplan, Meiqi Xu, Petra Seemann, J. M. Connor, David L. Glaser, Liam Carroll, Patricia Delai, Elisabeth Fastnacht-Urban, Stephen J. Forman, Gabriele Gillessen‐Kaesbach, Julie Hoover‐Fong, Bernhard Köster, Richard M. Pauli, William Reardon, Syed-Adeel Zaidi, Michael Zasloff, Rolf Morhart, Stefan Mundlos, Jay C. Groppe, Eileen M. Shore	2008	337
7	Size of the unstable CTG repeat sequence in relation to phenotype and parental transmission in myotonic dystrophy. PubMed ·Helen G. Harley, S A Rundle, J. MacMillan, J Myring, J. David Brook, Steve Crow, William Reardon, Iain Fenton, Duncan J. Shaw, P S Harper	1993	318
8	Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA The Lancet ·William Reardon, Marcus Pembrey, Richard C. Trembath, Richard Ross, Mary G. Sweeney, A. E. Harding, Linda Luxon	1992	309
9	Human Ehlers-Danlos Syndrome Type VII C and Bovine Dermatosparaxis Are Caused by Mutations in the Procollagen I N-Proteinase Gene The American Journal of Human Genetics ·Alain Colige, Aleksander L. Sieroń, Shi-Wu Li, Ulrike Schwarze, Elizabeth M. Petty, Wladimir Wertelecki, William R. Wilcox, Deborah Krakow, Daniel H. Cohn, William Reardon, Peter H. Byers, Charles M. Lapière, Darwin J. Prockop, Betty Nusgens	1999	297
10	Diversity and Function of Mutations in P450 Oxidoreductase in Patients with Antley-Bixler Syndrome and Disordered Steroidogenesis The American Journal of Human Genetics ·Ningwu Huang, Amit V. Pandey, Vishal Agrawal, William Reardon, Pablo Lapunzina, David Mowat, Ethylin Wang Jabs, Guy Van Vliet, Joseph Sack, Christa E. Flück, Walter L. Miller	2005	285
11	Heterozygous mutations in the gene encoding noggin affect human joint morphogenesis Nature Genetics ·Yaoqin Gong, Deborah Krakow, José Roberto Marcelino, Douglas J. Wilkin, David Chitayat, Riyana Babul‐Hirji, Louanne Hudgins, Cor W. R. J. Cremers, Frans P.M. Cremers, Han G. Brunner, Kent A. Reinker, David L. Rimoin, Daniel H. Cohn, Frances R. Goodman, William Reardon, Michael A. Patton, Clair A. Francomano, Matthew L. Warman	1999	273
12	Mutation and deletion of the pseudoautosomal gene SHOX cause Leri-Weill dyschondrosteosis Nature Genetics ·Deborah Shears, Humberto Vassal, Frances R. Goodman, Rodger W. Palmer, William Reardon, Andrea Superti‐Furga, Peter Scambler, Robin M. Winter	1998	259
13	A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis Nature Genetics ·Alison Ross, Víctor L. Ruiz‐Pérez, Yiming Wang, Donna-Marie Hagan, (unknown), Sally Ann Lynch, Susan Lindsay, Emily Jane Custard, Elena Belloni, David I. Wilson, Roy Wadey, Frances R. Goodman, Karen Helene Ørstavik, Tom Monclair, Steve Robson, William Reardon, John Burn, Peter Scambler, Tom Strachan	1998	229
14	Haploinsufficiency of TCF4 Causes Syndromal Mental Retardation with Intermittent Hyperventilation (Pitt-Hopkins Syndrome) The American Journal of Human Genetics ·Christiane Zweier, Maarit Peippo, Juliane Hoyer, Sérgio B. Sousa, Armand Bottani, Jill Clayton‐Smith, William Reardon, Jorge Saraiva, Alexandra Cabral, Ina Göhring, Koenraad Devriendt, Thomy de Ravel, Emilia K. Bijlsma, Raoul C. M. Hennekam, Alfredo Orrico, Monika Cohen, Alexander Dreweke, André Reis, Peter Nürnberg, Anita Rauch	2007	222
15	Anticipation in myotonic dystrophy: new light on an old problem. PubMed ·Peter S. Harper, H G Harley, William Reardon, Duncan J. Shaw	1992	215
16	Assisted reproductive therapies and imprinting disorders—a preliminary British survey Human Reproduction ·Alastair Sutcliffe, Catherine Peters, Sarah Bowdin, I. Karen Temple, William Reardon, Lisa M Wilson, Jill Clayton‐Smith, L A Brueton, Wendy Bannister, Eamonn R. Maher	2005	208
17	Radiological malformations of the ear in pendred syndrome Clinical Radiology ·Peter Phelps, Rebecca A. Coffey, Richard C. Trembath, Linda Luxon, Ashley Grossman, K. E. Britton, P. Kendall‐Taylor, John M. Graham, B.C. Cadge, S.G.D. Stephens, Marcus Pembrey, William Reardon	1998	199
18	Deletions at the SOX10 Gene Locus Cause Waardenburg Syndrome Types 2 and 4 The American Journal of Human Genetics ·Nadège Bondurand, Florence Dastot‐Le Moal, Laure Stanchina, Nathalie Collot, Viviane Baral, Sandrine Marlin, Tania Attié‐Bitach, Irina Giurgea, Laurent Skopinski, William Reardon, Annick Toutain, Pierre Sarda, Echaieb Anis, Marilyn Lackmy-Port-Lis, Renaud Touraine, Jeanne Amiel, Michel Goossens, Véronique Pingault	2007	198
19	Molecular Analysis of the Pds Gene in Pendred Syndrome (Sensorineural Hearing Loss and Goitre) Human Molecular Genetics ·Beth Coyle, William Reardon, Jo-Anne Herbrick, L.‐C. Tsui, Eleanor Gausden, Ju Hee Lee, Rebecca Coffey, Annette Grueters, Ashley Grossman, Peter Phelps, Linda Luxon, P. Kendall‐Taylor, Stephen W. Scherer, Richard C. Trembath	1998	191
20	Williams Syndrome: Use of Chromosomal Microdeletions as a Tool to Dissect Cognitive and Physical Phenotypes The American Journal of Human Genetics ·Mayada Tassabehji, Kay Metcalfe, Annette Karmiloff‐Smith, Martin J. Carette, Julia D. Grant, N R Dennis, William Reardon, Miranda Splitt, Andrew Read, D Donnai	1999	180

About William Reardon

William Reardon is a scholar working on Genetics, Molecular Biology, Surgery, Pediatrics, Perinatology and Child Health and Sensory Systems, having authored 196 papers that have together received 12.4k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (28 papers), Hearing, Cochlea, Tinnitus, Genetics (23 papers), Cleft Lip and Palate Research (21 papers), Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (18 papers), Genetics and Neurodevelopmental Disorders (18 papers), Congenital heart defects research (17 papers) and Connective tissue disorders research (15 papers). The work is most often cited by research in Sensory Systems (1.5k citations), Genetics (5.2k citations), Developmental Biology (324 citations), Otorhinolaryngology (456 citations) and Molecular Biology (6.1k citations). William Reardon has collaborated with scholars based in United Kingdom, Ireland and United States. Frequent co-authors include Robin M. Winter, Paul Rutland, Louise J. Pulleyn, Sue Malcolm, Richard C. Trembath, Barry M. Jones, R M Winter, Marcus Pembrey, J. David Brook and Richard Hayward. Their work appears in journals such as Journal of Medical Genetics, The American Journal of Human Genetics, European Journal of Human Genetics, Nature Genetics and Clinical 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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William Reardon

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William Reardon

William Reardon's Hit Papers

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About William Reardon

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