Jane A. Hurst

18.9k citations

85 papers · 7.7k indexed · 3 hit papers · h-index 34

Impact in

Endocrine and Autonomic Systems top 0.2%
- Regulation of Appetite and Obesity
Developmental Biology top 1%

Papers in ⓘ

Developmental Biology 9
- Congenital limb and hand anomalies 9
Genetics 52
- Craniofacial Disorders and Treatments 11
- Connective tissue disorders research 10
- Genomics and Rare Diseases 10
- Genetic Syndromes and Imprinting 7
- Genomic variations and chromosomal abnormalities 7
- Cleft Lip and Palate Research 7

Co-authors: Anthony P. Monaco (2 shared papers)Faraneh Vargha‐Khadem (2 shared papers)Cecilia Lai (2 shared papers)Simon E. Fisher (2 shared papers)Elizabeth Montague (1 shared paper)Harald Rau (1 shared paper)Nicholas J. Wareham (1 shared paper)Maria A. Soos (1 shared paper)
Journals: Journal of Medical Genetics (11 papers)European Journal of Human Genetics (5 papers)Nature Genetics (4 papers)Clinical Genetics (4 papers)The American Journal of Human Genetics (3 papers)
Partner nations: United Kingdom United States Canada

In The Last Decade

Jane A. Hurst

84 papers receiving 7.4k citations

Hit Papers

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Mutations in a new member of the chromodomain gene family cause CHARGE syndrome 2004 · 876 citations

Peers

Countries citing papers authored by Jane A. Hurst

Since Specialization

Citations

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

Fields of papers citing papers by Jane A. Hurst

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jane A. Hurst. 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 Jane A. Hurst. The network helps show where Jane A. Hurst may publish in the future.

Co-authors

The 25 scholars most cited alongside Jane A. Hurst, 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 Jane A. Hurst Line = papers co-authored together Jane A. Hurst 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 85 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Congenital leptin deficiency is associated with severe early-onset obesity in humans Nature ·Elizabeth Montague, I. Sadaf Farooqi, Jonathan P. Whitehead, Maria A. Soos, Harald Rau, Nicholas J. Wareham, Ciaran Sewter, Janet E. Digby, Shehla Mohammed, Jane A. Hurst, Christopher H. Cheetham, Alison R. Earley, Anthony Barnett, Johannes B. Prins, Stephen O’Rahilly Hit paper breakdown →	1997	2182
2	A forkhead-domain gene is mutated in a severe speech and language disorder Nature ·Cecilia Lai, Simon E. Fisher, Jane A. Hurst, Faraneh Vargha‐Khadem, Anthony P. Monaco Hit paper breakdown →	2001	1282
3	Mutations in a new member of the chromodomain gene family cause CHARGE syndrome Nature Genetics ·Lisenka E.L.M. Vissers, Conny M.A. van Ravenswaaij, R.J.C. Admiraal, Jane A. Hurst, Bert B.A. de Vries, Irene M. Janssen, W A van der Vliet, Erik Huys, Pieter J. de Jong, Ben C.J. Hamel, Eric Schoenmakers, Han G. Brunner, Joris A. Veltman, Ad Geurts van Kessel Hit paper breakdown →	2004	876
4	Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome Nature Genetics ·Andrew J. Sharp, S.K. Hansen, Rebecca R. Selzer, Ze Cheng, Regina Regan, Jane A. Hurst, Helen Stewart, Sue Price, Edward Blair, Raoul C. M. Hennekam, Carrie Fitzpatrick, Rick Segraves, Todd Richmond, Cheryl Guiver, Donna G. Albertson, Daniel Pinkel, Peggy S. Eis, Stuart Schwartz, Samantha J.L. Knight, Evan E. Eichler	2006	429
5	An extended Family with a Dominantly Inherited Speech Disorder Developmental Medicine & Child Neurology ·Jane A. Hurst, M Baraitser, Eric Auger, Francisco Julio Pellicer Graham, Stefan Norell	1990	238
6	Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification Nature Genetics ·Andrew O.M. Wilkie, Zequn Tang, Navaratnam Elanko, Sinéad Walsh, Stephen R.F. Twigg, Jane A. Hurst, Steven A. Wall, Krystyńa Chrzańowska, Robert E. Maxson	2000	216
7	Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis PEDIATRICS ·Andrew O.M. Wilkie, Jo C. Byren, Jane A. Hurst, Jayaratnam Jayamohan, David Johnson, Samantha J.L. Knight, Tracy Lester, Peter G. Richards, Stephen R.F. Twigg, Steven A. Wall	2010	194
8	The SPCH1 Region on Human 7q31: Genomic Characterization of the Critical Interval and Localization of Translocations Associated with Speech and Language Disorder The American Journal of Human Genetics ·Cecilia Lai, Simon E. Fisher, Jane A. Hurst, Elaine R. Levy, Shirley Hodgson, Margaret Fox, S. JEREMIAH, S. Povey, D. Curtis Jamison, Eric D. Green, Faraneh Vargha‐Khadem, Anthony P. Monaco	2000	147
9	Improving diagnosis and broadening the phenotypes in early-onset seizure and severe developmental delay disorders through gene panel analysis Journal of Medical Genetics ·Natalie Trump, Amy McTague, Helen Brittain, Apostolos Papandreou, Esther Meyer, Adeline Ngoh, Rodger Palmer, Deborah Morrogh, C. R. Boustred, Jane A. Hurst, Lucy Jenkins, Manju A. Kurian, Richard H. Scott	2016	147
10	Simpson-Golabi-Behmel syndrome: Genotype/phenotype analysis of 18 affected males from 7 unrelated families American Journal of Medical Genetics ·R Hughes-Benzie, Giuseppe Pilia, J.Y. Xuan, Alasdair G. W. Hunter, Ellson Chen, Mahin Golabi, Jane A. Hurst, J. Kobori, Kathi Marymee, Roberta A Pagon, Hope H. Punnett, Susan Schelley, John Tolmie, Monica M. Wohlferd, Tom Grossman, David Schlessinger, Alex MacKenzie	1996	109
11	Homozygous Nonsense Mutations in KIAA1279 Are Associated with Malformations of the Central and Enteric Nervous Systems The American Journal of Human Genetics ·Alice S. Brooks, Aida M. Bertoli‐Avella, Grzegorz Burzynski, Guido J. Breedveld, Jan Osinga, Ludolf G. Boven, Jane A. Hurst, Grazia M.S. Mancini, Maarten H. Lequin, I.F.M. de Coo, Ivana Matera, Esther de Graaff, Carel Meijers, Patrick J. Willems, Dick Tibboel, Ben A. Oostra, Robert M.W. Hofstra	2005	106
12	Frontorhiny, a Distinctive Presentation of Frontonasal Dysplasia Caused by Recessive Mutations in the ALX3 Homeobox Gene The American Journal of Human Genetics ·Stephen R.F. Twigg, Sarah L. Versnel, Gudrun Nürnberg, Melissa Lees, Meenakshi Bhat, Peter Hammond, Raoul C. M. Hennekam, A. Jeannette M. Hoogeboom, Jane A. Hurst, David H. Johnson, Alexis Robinson, Peter Scambler, Dianne Gerrelli, Peter Nürnberg, Irene M.J. Mathijssen, Andrew O.M. Wilkie	2009	93
13	Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children Journal of Medical Genetics ·Lamia Mestek, Emma Clement, Wendy D. Jones, Suzanne Drury, Louise Ocaka, Andrey Gagunashvili, Polona Le Quesne Stabej, Chiara Bacchelli, Nital Jani, Shamima Rahman, Lucy Jenkins, Jane A. Hurst, Maria Bitner‐Glindzicz, Mark Peters, Philip L. Beales, Hywel Williams	2018	89
14	Mutations in FAM20C also identified in non‐lethal osteosclerotic bone dysplasia Clinical Genetics ·Michael A. Simpson, Angela E. Scheuerle, Jane A. Hurst, Patton Ma, Helen Stewart, Andrew H. Crosby	2009	88
15	Clinical dividends from the molecular genetic diagnosis of craniosynostosis American Journal of Medical Genetics Part A ·Andrew O.M. Wilkie, Elena G. Bochukova, Ruth M. S. Hansen, Indira B. Taylor, Sahan V. Rannan‐Eliya, Jo C. Byren, Steven A. Wall, Lina Ramos, Margarida Venâncio, Jane A. Hurst, A O'Rourke, Louise Williams, A Seller, Tracy Lester	2006	80
16	Clinical dividends from the molecular genetic diagnosis of craniosynostosis† American Journal of Medical Genetics Part A ·Andrew O.M. Wilkie, Elena G. Bochukova, Ruth M. S. Hansen, Indira B. Taylor, Sahan V. Rannan‐Eliya, Jo C. Byren, Steven A. Wall, Lina Ramos, Margarida Venâncio, Jane A. Hurst, A O'Rourke, Louise Williams, A Seller, Tracy Lester	2007	66
17	A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype–phenotype correlations in type XI collagenopathies American Journal of Medical Genetics Part A ·Marja Majava, Kristien Hoornaert, Deborah Bartholdi, Mieke C. Bouma, Katelijne Bouman, Marta Carrera, Koenraad Devriendt, Jane A. Hurst, George Kitsos, Dunja Niedrist, Michael B. Petersen, Debbie Shears, Irene Stolte‐Dijkstra, Johanna M. van Hagen, Leena Ala‐Kokko, Minna Männikkö, Geert Mortier	2007	61
18	Phenotypic variability in 49 cases of ESCO2 mutations, including novel missense and codon deletion in the acetyltransferase domain, correlates with ESCO2 expression and establishes the clinical criteria for Roberts syndrome Journal of Medical Genetics ·Horacio Astudillo‐de la Vega, Alison Trainer, Miriam Gordillo, Moira Crosier, Hülya Kayserili, Flemming Skovby, Maria Luisa Giovannucci Uzielli, Rhonda E. Schnur, Sylvie Manouvrier, E Blair, Jane A. Hurst, Francesca Forzano, Moritz Meins, K. O. J. Simola, Annick Raas‐Rothschild, Raoul C. M. Hennekam, Ethylin Wang Jabs	2009	61
19	Large scale deletions in the GPC3 gene may account for a minority of cases of Simpson-Golabi-Behmel syndrome. Journal of Medical Genetics ·Susan Lindsay, Mark Ireland, Ottie O’Brien, Jill Clayton‐Smith, Jane A. Hurst, Jeff Mann, Tim Cole, J Sampson, S Slaney, David Schlessinger, John Burn, Giuseppe Pilia	1997	58
20	Malan syndrome: Sotos-like overgrowth with de novo NFIX sequence variants and deletions in six new patients and a review of the literature European Journal of Human Genetics ·Merel Klaassens, Deborah Morrogh, Elisabeth Rosser, Fatima Jaffer, Maaike Vreeburg, Levinus A. Bok, Tim Segboer, Martine van Belzen, Rosaline C. M. Quinlivan, Ajith Kumar, Jane A. Hurst, Richard H. Scott	2014	48

About Jane A. Hurst

Jane A. Hurst is a scholar working on Developmental Biology, Genetics, Genetics, Molecular Biology and Clinical Biochemistry, having authored 85 papers that have together received 7.7k indexed citations. Recurring topics across this work include Craniofacial Disorders and Treatments (11 papers), Connective tissue disorders research (10 papers), Genomics and Rare Diseases (10 papers), Congenital limb and hand anomalies (9 papers), Genetic Syndromes and Imprinting (7 papers), Genomic variations and chromosomal abnormalities (7 papers), Cleft Lip and Palate Research (7 papers) and Congenital heart defects research (6 papers). The work is most often cited by research in Endocrine and Autonomic Systems (1.7k citations), Developmental Biology (286 citations), Genetics (3.1k citations), Nutrition and Dietetics (955 citations) and Genetics (595 citations). Jane A. Hurst has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Anthony P. Monaco, Faraneh Vargha‐Khadem, Cecilia Lai, Simon E. Fisher, Elizabeth Montague, Harald Rau, Nicholas J. Wareham, Maria A. Soos, Anthony Barnett and Johannes B. Prins. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, Nature Genetics, Clinical Genetics and The American Journal of Human 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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