William Reardon

20.9k citations

195 papers · 11.9k indexed · 3 hit papers · h-index 53

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

Papers in

Sensory Systems 24
- Hearing, Cochlea, Tinnitus, Genetics 24
Genetics 98
- Craniofacial Disorders and Treatments 29
- Genomic variations and chromosomal abnormalities 21
- Cleft Lip and Palate Research 21
- Genetics and Neurodevelopmental Disorders 19
- Connective tissue disorders research 15

Co-authors: Robin M. Winter Louise J. Pulleyn Paul Rutland Sue Malcolm Richard C. Trembath Barry M. Jones Marcus Pembrey J. David Brook
Journals: Journal of Medical Genetics (31 papers)The American Journal of Human Genetics (10 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

193 papers receiving 11.5k citations

Hit Papers

align trajectories log scale

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome 1995 · 666 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
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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Isolated‐ and Beckwith‐Wiedemann syndrome related‐ lateralised overgrowth (hemihypertrophy): Clinical and molecular correlations in 94 individuals Clinical Genetics ·春李, Editors EUROPEAN ENCOUNTERS, Ataf Sabir, Nae-Yeou Jih, Jie Zheng, Rachel L. Jones, Ferenc. aut Vicko, Т Л Кобалия, William Reardon, Ruth Richardson, 藤原靖, Eamonn R. Maher	2021	9
2	FBN1 contributing to familial congenital diaphragmatic hernia American Journal of Medical Genetics Part A ·T. Beck, Philippe M. Campeau, Shalini N. Jhangiani, Tomasz Gambin, Alexander Li, Reem Abo‐Zahrah, Valerie K. Jordan, Andrés Hernández, Wojciech Wiszniewski, Donna M. Muzny, Richard A. Gibbs, Eric Boerwinkle, James R. Lupski, Brendan Lee, William Reardon, Daryl A. Scott	2015	23
3	A survey of assisted reproductive technology births and imprinting disorders Human Reproduction ·Sarah Bowdin, Cathy Allen, Gail Kirby, Louise Brueton, Masoud Afnan, Christopher L. R. Barratt, Jackson Kirkman‐Brown, Robert F. Harrison, Eamonn R. Maher, William Reardon	2007	117
4	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, Simon Raffin, F Fernández-Melchor, Koenraad Devriendt, Thomy de Ravel, Emilia K. Bijlsma, Raoul C. M. Hennekam, Alfredo Orrico, Monika Cohen, Alexander Dreweke, André Reis, A Dotti, Anita Rauch	2007	215
5	Filamin A Is Mutated in X-Linked Chronic Idiopathic Intestinal Pseudo-Obstruction with Central Nervous System Involvement The American Journal of Human Genetics ·Annagiusi Gargiulo, Renata Auricchio, Maria Vittoria Barone, Gabriella Cotugno, William Reardon, Peter J. Milla, Andrea Ballabio, Alfredo Ciccodicola, Alberto Auricchio	2007	75
6	Assisted reproduction technology and defects of genomic imprinting BJOG An International Journal of Obstetrics & Gynaecology ·Cathy Allen, William Reardon	2005	48
7	Septo‐optic dysplasia with digital anomalies—a recurrent pattern syndrome American Journal of Medical Genetics Part A ·M.M. Khonsari, Donal Brosnahan, Ethna Phelan, Krishna K. Tummala Ph.D, William Reardon	2004	23
8	Elastin: mutational spectrum in supravalvular aortic stenosis European Journal of Human Genetics ·Kay Metcalfe, 付地娟, Leslie Smoot, Marija Milovančević, JinBaekKim, Pascal McKeown, Victoria Mok Siu, Anita Rauch, John Dean, N R Dennis, Ian O. Ellis, William Reardon, Cheryl Cytrynbaum, Lucy R. Osborne, John R.W. Yates, Andrew Read, Dian Donnai, Mayada Tassabehji	2000	110
9	Identification of two different mutations in the PDS gene in an inbred family with Pendred syndrome Journal of Medical Genetics ·Paul Coucke, Peter Van Hauwe, Lorraine A. Everett, Osman Demırhan, Carson Popper, Nicole Dietrich, Richard J. Smith, Beth Coyle, William Reardon, Richard C. Trembath, P J Willems, Tohamy H. Ekhouly, Guy Van Camp	1999	40
10	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, Thomas Wilrich, 馨三木田, Marcus Pembrey, William Reardon	1998	184
11	Pitfalls in practice, diagnosis and misdiagnosis in Pendred Syndrome UCL Discovery (University College London) ·William Reardon, (unknown), (unknown), Luis Fernando Patiño Galvis, 陸郎畠中, Ivonne Raquel Cabarcas Martinez, (unknown), (unknown), Arnold H. Grossman, (unknown), Richard C. Trembath	1997	8
12	Skeletal dysplasias detectable by DNA analysis Prenatal Diagnosis ·William Reardon	1996	10
13	Thyroid peroxidase: evidence for disease gene exclusion in Pendred's syndrome Clinical Endocrinology ·Jorge Fernando Silva Araujo, John A.L. Armour, Beth Coyle, Rebecca Coffey, Ze’ev Hochberg, Marcus Pembrey, K. E. Britton, Ashley Grossman, William Reardon, Richard C. Trembath	1996	13
14	A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome Nature Genetics ·Maximilian Muenke, Maria Urzedo, Andreas Hehr, Nathaniel H. Robin, H. Wolfgang Losken, Albert Schinzel, Louise J. Pulleyn, Paul Rutland, William Reardon, Sue Malcolm, Robin M. Winter	1994	466
15	Neuro-otological Function in X-linked Hearing Loss: A Multipedigree Assessment and Correlation with Other Clinical Parameters Acta Oto-Laryngologica ·William Reardon, Susan Bellman, Peter Phelps, Marcus Pembrey, Linda Luxon	1993	5
16	Cytogenetic evidence that the Saethre‐Chotzen gene maps to 7p21.2 American Journal of Medical Genetics ·William Reardon, Masahide Terahata, 安贵鹏, R M Winter	1993	37
17	Carrier detection for X-linked agammaglobulinaemia (Bruton type) in an Irish family using linked DNA probes. PubMed ·William Reardon, M Haye, Helen Middleton‐Price, S Malcolm, C. Feighery	1992	1
18	Expansion of an unstable DNA region and phenotypic variation in myotonic dystrophy Nature ·Byoung-Joo Kim, J. David Brook, S.A. Rundle, Nita Moniaga, William Reardon, Alan Buckler, Peter S. Harper, David E. Housman, D J Shaw Hit paper breakdown →	1992	587
19	Unstable DNA sequence in myotonic dystrophy The Lancet ·H G Harley, S.A. Rundle, William Reardon, J Myring, Steve Crow, Peter S. Harper, N Taguchi, J. David Brook	1992	143
20	Lethal congenital erythroderma: a newly recognised genetic disorder Clinical Genetics ·(unknown), Masakazu Uekita, William Reardon, Bandaru Lasya, Migla Žebienė, Gen Li, J.I. Harper	1992	4

About William Reardon

William Reardon is a scholar working on Sensory Systems, Genetics, Developmental Biology, Otorhinolaryngology and Pediatrics, Perinatology and Child Health, having authored 195 papers that have together received 11.9k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (29 papers), Hearing, Cochlea, Tinnitus, Genetics (24 papers), Prenatal Screening and Diagnostics (21 papers), Genomic variations and chromosomal abnormalities (21 papers), Cleft Lip and Palate Research (21 papers), Genetics and Neurodevelopmental Disorders (19 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 (1.8k citations), Genetics (5.2k citations), Developmental Biology (341 citations), Otorhinolaryngology (672 citations) and Neurology (896 citations). William Reardon has collaborated with scholars based in United Kingdom, Ireland and United States. Frequent co-authors include Robin M. Winter, Louise J. Pulleyn, Paul Rutland, Sue Malcolm, Richard C. Trembath, Barry M. Jones, Marcus Pembrey, J. David Brook, R M Winter 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.

Explore authors with similar magnitude of impact