Regina Regan

11.3k citations

27 papers · 2.5k indexed · h-index 18

Genetics top 0.5%
Molecular Biology top 10%
Plant Science top 5%
Pediatrics, Perinatology and Child Health top 2%
Physiology

Co-authors: Samantha J.L. Knight Jonathan Flint Robert E. Kearney Sharon W. Horsley A Nicod D. L. N. Cardy N. M. Lawrie Raoul C. M. Hennekam
Topics: Genomic variations and chromosomal abnormalities (17 papers)Genetics and Neurodevelopmental Disorders (9 papers)Chromosomal and Genetic Variations (8 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Plant Science
Journals: The Lancet Nature Genetics PLoS ONE
Partner nations: United Kingdom United States Netherlands

In The Last Decade

Regina Regan

27 papers receiving 2.5k citations

Peers

Countries citing papers authored by Regina Regan

Since Specialization

Citations

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

Fields of papers citing papers by Regina Regan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Regina Regan

This figure shows the co-authorship network connecting the top 25 collaborators of Regina Regan. A scholar is included among the top collaborators of Regina Regan based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Regina Regan. Regina Regan is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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

20 of 20 papers shown

#	Work	Indexed citations
1	Identification of a mutation in LARS as a novel cause of infantile hepatopathy 2012 ·Molecular Genetics and Metabolism ·Jillian P. Casey,Paul McGettigan,Niamh Lynam‐Lennon,Michael McDermott,Regina Regan,Judith Conroy,Billy Bourke,(unknown),Ellen Crushell,Sally Ann Lynch,Sean Ennis	68
2	First implication ofSTRA6mutations in isolated anophthalmia, microphthalmia, and coloboma: A new dimension to theSTRA6phenotype 2011 ·Human Mutation ·Jillian P. Casey,Riki Kawaguchi,(unknown),Hui Sun,Paul McGettigan,Jens Erik Nielsen,Judith Conroy,Regina Regan,Elaine Kenny,Paul Cormican,Derek W. Morris,(unknown),Muireann Ní Chróinín,Breandán N. Kennedy,Sally Ann Lynch,Andrew Green,Sean Ennis	64
3	Genomic Imbalances Are Confined to Non-Proliferating Cells in Paediatric Patients with Acute Myeloid Leukaemia and a Normal or Incomplete Karyotype 2011 ·PLoS ONE ·Erica Ballabio,Regina Regan,(unknown),Jochen Harbott,Jutta Bradtke,Andrea Teigler‐Schlegel,Andrea Biondi,Giovanni Cazzaniga,Giovanni De Giudici,James S. Wainscoat,Jacqueline Boultwood,Joanna M. Bridger,Samantha J.L. Knight,Sabrina Tosi	3
4	The 12q14 microdeletion syndrome: six new cases confirming the role of HMGA2 in growth 2011 ·European Journal of Human Genetics ·Sally Ann Lynch,Nicola Foulds,Ann‐Charlotte Thuresson,Amanda Collins,Göran Annerén,(unknown),Carol A. Delaney,James Iremonger,(unknown),John A. Crolla,Colm Costigan,Wayne Lam,David Fitzpatrick,Regina Regan,Sean Ennis,Freddie H. Sharkey	33
5	Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant 2008 ·Journal of Medical Genetics ·Femke Hannes,Andrew J. Sharp,Heather C. Mefford,Thomy de Ravel,Claudia Ruivenkamp,M.H. Breuning,JP Fryns,Koenraad Devriendt,Griet Van Buggenhout,Annick Vogels,Helen Stewart,Raoul C. M. Hennekam,Gregory M. Cooper,Regina Regan,Samantha J.L. Knight,Evan E. Eichler,Joris Vermeesch	207
6	Diagnosing idiopathic learning disability: a cost-effectiveness analysis of microarray technology in the National Health Service of the United Kingdom 2007 ·PubMed ·Sarah Wordsworth,James Buchanan,Regina Regan,Val Davison,(unknown),Sara Dyer,Carolyn Campbell,Edward Blair,(unknown),Jenny C. Taylor,Samantha J.L. Knight	27
7	Characterization of a recurrent 15q24 microdeletion syndrome 2007 ·Human Molecular Genetics ·Andrew J. Sharp,Rebecca R. Selzer,Joris A. Veltman,Stefania Gimelli,Giorgio Gimelli,Pasquale Striano,Antonietta Coppola,Regina Regan,Sue Price,Nine V.A.M. Knoers,Peggy S. Eis,Han G. Brunner,Raoul C. M. Hennekam,Samantha J.L. Knight,Bert B.A. de Vries,Orsetta Zuffardi,(unknown)	129
8	Identification of non-recurrent submicroscopic genome imbalances: the advantage of genome-wide microarrays over targeted approaches 2007 ·European Journal of Human Genetics ·David A. Koolen,Erik A. Sistermans,(unknown),Samantha J.L. Knight,Regina Regan,(unknown),R. Frank Kooy,Liesbeth Rooms,Corrado Romano,Marco Fichera,Albert Schinzel,Alessandra Baumer,Britt-Marie Anderlid,Jacqueline Schoumans,Ad Geurts van Kessel,Magnus Nordenskjöld,Bert B.A. de Vries	12
9	A new chromosome 17q21.31 microdeletion syndrome associated with a common inversion polymorphism 2006 ·Nature Genetics ·David A. Koolen,Lisenka E.L.M. Vissers,Rolph Pfundt,Nicole de Leeuw,Samantha J.L. Knight,Regina Regan,R. Frank Kooy,Edwin Reyniers,Corrado Romano,Marco Fichera,Albert Schinzel,Alessandra Baumer,Britt-Marie Anderlid,Jacqueline Schoumans,Nine V.A.M. Knoers,Ad Geurts van Kessel,Erik A. Sistermans,Joris A. Veltman,Han G. Brunner,Bert B.A. de Vries	305
10	Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome 2006 ·Nature Genetics ·Andrew J. Sharp,(unknown),Rebecca R. Selzer,Ze Cheng,Regina Regan,Jane A. Hurst,Helen Stewart,Sue Price,Edward Blair,Raoul C. M. Hennekam,Carrie Fitzpatrick,(unknown),Todd Richmond,(unknown),Donna G. Albertson,Daniel Pinkel,Peggy S. Eis,Stuart Schwartz,Samantha J.L. Knight,Evan E. Eichler	429
11	Screening of subtelomeric rearrangements in autistic disorder: Identification of a partial trisomy of 13q34 in a patient bearing a 13q;21p translocation 2006 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Maria Antonietta Di Bella,Francesco Calı̀,Gregorio Seidita,Mario G. Mirisola,Angela Ragusa,(unknown),Ornella Galesi,Maurizio Elia,Donatella Greco,Marinella Zingale,(unknown),(unknown),Regina Regan,(unknown),Alessia Gallo,Valentino Romano	11
12	Submicroscopic 8pter deletion, mild mental retardation, and behavioral problems caused by a familial t(8;20)(p23;p13) 2001 ·American Journal of Medical Genetics ·Bert B.A. de Vries,Melissa Lees,Samantha J.L. Knight,Regina Regan,(unknown),Jonathan Flint,Angela Barnicoat,Robin M. Winter	18
13	Screening for subtelomeric chromosome abnormalities in children with idiopathic mental retardation using multiprobe telomeric FISH and the new MAPH telomeric assay 2001 ·European Journal of Human Genetics ·Carolina Sismani,John A.L. Armour,Jonathan Flint,(unknown),Regina Regan,Philippos C. Patsalis	53
14	Navajo poikiloderma with cyclic neutropenia in Turkish children, clinical description and exclusion of linkage to the Rothmund Thomson RECQL4 gene 2000 ·The American Journal of Human Genetics ·Nora Shannon,Regina Regan,Edna L. Maltby,Jonathan Flint,Alan S. Rigby,(unknown),(unknown)	1
15	An Optimized Set of Human Telomere Clones for Studying Telomere Integrity and Architecture 2000 ·The American Journal of Human Genetics ·Samantha J.L. Knight,Christa M. Lese,Kathrin S. Precht,(unknown),(unknown),Sarah Lucas,Regina Regan,Mary Brenan,A Nicod,N. M. Lawrie,D. L. N. Cardy,Huy Nguyen,Thomas J. Hudson,Harold Riethman,David H. Ledbetter,Jonathan Flint	237
16	Neurodevelopmental profile of a new dysmorphic syndrome associated with submicroscopic partial deletion of 1p36.3 2000 ·Developmental Medicine & Child Neurology ·(unknown),Samantha J.L. Knight,Helen Heussler,Regina Regan,Jonathan Flint,Katherine Martin	29
17	Subtle chromosomal rearrangements in children with unexplained mental retardation 1999 ·The Lancet ·Samantha J.L. Knight,Regina Regan,A Nicod,Sharon W. Horsley,Robert E. Kearney,Tessa Homfray,Robin M. Winter,Patrick Bolton,Jonathan Flint	325
18	cDNA Cloning of a Humandishevelled DVL-3Gene, Mapping to 3q27, and Expression in Human Breast and Colon Carcinomas 1997 ·Biochemical and Biophysical Research Communications ·(unknown),David R. Beier,(unknown),Kenneth Smith,(unknown),(unknown),Robert E. Kearney,Regina Regan,Daniel J. Sussman,Adrian L. Harris	18
19	Mallory bodies: isolation of hepatocellular hyalin and electrophoretic resolution of polypeptide components. 1978 ·PubMed ·Harold M. Tinberg,Regina Regan,(unknown),(unknown),Samuel W. French	33
20	The influence of surface rugosity on haemolysis occurring in tubing. 1976 ·PubMed ·(unknown),(unknown),Regina Regan	4

About Regina Regan

Regina Regan is a scholar working on Genetics, Plant Science and Critical Care and Intensive Care Medicine, having authored 27 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Chromosomal and Genetic Variations (8 papers). The work is most often cited by research in Genetics (2.1k citations), Pediatrics, Perinatology and Child Health (472 citations) and Plant Science (778 citations). Regina Regan has collaborated with scholars based in United Kingdom, United States and Netherlands. Frequent co-authors include Samantha J.L. Knight, Jonathan Flint, Robert E. Kearney, Sharon W. Horsley, A Nicod, D. L. N. Cardy, N. M. Lawrie, Raoul C. M. Hennekam, Andrew J. Sharp and Robin M. Winter. Their work appears in journals such as The Lancet, Nature Genetics and PLoS ONE.

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