Morag N. Collinson

2.2k citations

21 papers · 473 indexed · h-index 14

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

Co-authors: John Barber John A. Crolla Shuwen Huang Patricia A. Jacobs N R Dennis Katherine Lachlan Viv Maloney N. Simon Thomas
Topics: Genomic variations and chromosomal abnormalities (16 papers)Prenatal Screening and Diagnostics (7 papers)Genetics and Neurodevelopmental Disorders (5 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: Journal of Medical Genetics Human Genetics Genetics in Medicine
Partner nations: United Kingdom United States Norway

In The Last Decade

Morag N. Collinson

21 papers receiving 412 citations

Peers

Countries citing papers authored by Morag N. Collinson

Since Specialization

Citations

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

Fields of papers citing papers by Morag N. Collinson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Morag N. Collinson. 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 Morag N. Collinson. The network helps show where Morag N. Collinson may publish in the future.

Co-authorship network of co-authors of Morag N. Collinson

This figure shows the co-authorship network connecting the top 25 collaborators of Morag N. Collinson. A scholar is included among the top collaborators of Morag N. Collinson 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 Morag N. Collinson. Morag N. Collinson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Directly Transmitted 12.3-Mb Deletion with a Consistent Phenotype in the Variable 11q21q22.3 Region 2020 ·Cytogenetic and Genome Research ·(unknown),Mira Kharbanda,Mark S. Bateman,David Hunt,(unknown),Amanda Collins,David J. Bunyan,Morag N. Collinson,(unknown),(unknown),John Barber	1
2	Exon-focused targeted oligonucleotide microarray design increases detection of clinically relevant variants across multiple NHS genomic centres 2020 ·npj Genomic Medicine ·(unknown),(unknown),Angharad Williams,(unknown),(unknown),Morag N. Collinson,Sarah J. Beal,Sian Corrin,Siân Morgan	2
3	Mosaic Turner syndrome shows reduced penetrance in an adult population study 2018 ·Genetics in Medicine ·Marcus A. Tuke,Katherine S. Ruth,Andrew R. Wood,Robin N. Beaumont,Jessica Tyrrell,Samuel E. Jones,Hanieh Yaghootkar,Claire Turner,(unknown),Antonia Brooke,Morag N. Collinson,Rachel M. Freathy,Michael N. Weedon,Timothy M. Frayling,Anna Murray	86
4	Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities 2017 ·American Journal of Medical Genetics Part A ·Mark S. Bateman,Morag N. Collinson,David J. Bunyan,Amanda Collins,(unknown),(unknown),Victoria Harrison,Tessa Homfray,Shuwen Huang,(unknown),Katherine Lachlan,Viv Maloney,John Barber	5
5	Inherited 2q23.1 microdeletions involving the MBD5 locus 2017 ·Molecular Genetics & Genomic Medicine ·(unknown),Rubin Wang,Jonathan J. Waters,Christine Waterman,Amanda Collins,Morag N. Collinson,Joo Wook Ahn,Dragana Josifova,(unknown),Ajith Kumar	6
6	Expanding the ocular phenotype of 14q terminal deletions: A novel presentation of microphthalmia and coloboma in ring 14 syndrome with associated 14q32.31 deletion and review of the literature 2016 ·American Journal of Medical Genetics Part A ·Claire Salter,Diana Baralle,Morag N. Collinson,Jay Self	5
7	Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance 2015 ·American Journal of Medical Genetics Part A ·John Barber,Jill A. Rosenfeld,John M. Graham,Nancy Kramer,Katherine Lachlan,Mark S. Bateman,Morag N. Collinson,(unknown),Claire Turner,(unknown),Tyler Reimschisel,Athar M. Qureshi,(unknown),Mervyn Humphreys,Michael Marble,Taosheng Huang,Sarah J. Beal,(unknown),(unknown),Sarah Wynn	28
8	Pallister-Killian syndrome: a study of 22 British patients 2015 ·Journal of Medical Genetics ·Moira Blyth,Viv Maloney,Sarah J. Beal,Morag N. Collinson,Shuwen Huang,John A. Crolla,I. Karen Temple,Diana Baralle	33
9	Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletions 2010 ·American Journal of Medical Genetics Part A ·Marjolein H. Willemsen,Nicole de Leeuw,Catherine Mercer,(unknown),J. Glenn Morris,Morag N. Collinson,John Barber,Stephen T.S. Lam,Ivan F. M. Lo,(unknown),(unknown),Ben C.J. Hamel,Tjitske Kleefstra	6
10	Symmetrical enchondromatosis is associated with duplication of 12p11.23 to 12p11.22 including PTHLH 2010 ·American Journal of Medical Genetics Part A ·Morag N. Collinson,(unknown),Jocelyn Charlton,John A. Crolla,Caroline Silve,Christine M Hall,(unknown),(unknown),Sarah Smithson	17
11	Inverted duplication of 1q32.1 to 1q44 characterized by array CGH and review of distal 1q partial trisomy 2009 ·American Journal of Medical Genetics Part A ·Meena Balasubramanian,John Barber,Morag N. Collinson,Shuwen Huang,Viv Maloney,(unknown),(unknown)	24
12	15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q 2009 ·American Journal of Medical Genetics Part A ·Katrina Tatton‐Brown,Daniela T. Pilz,Karen Helene Ørstavik,Michael A. Patton,John Barber,Morag N. Collinson,V.K. Maloney,Shuwen Huang,John A. Crolla,Karen Marks,(unknown),Peter Thompson,Zafar Nawaz,(unknown),Susan Tomkins,(unknown),Nazneen Rahman,Meriel McEntagart	55
13	Functional disomy resulting from duplications of distal Xq in four unrelated patients 2004 ·Human Genetics ·Katherine Lachlan,Morag N. Collinson,Richard Sandford,(unknown),Patricia A. Jacobs,N. Simon Thomas	39
14	Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences 2004 ·European Journal of Human Genetics ·John Barber,N. Simon Thomas,Morag N. Collinson,N R Dennis,Thomas Liehr,Anja Weise,Britta Belitz,Lutz Pfeiffer,Maria Kirchhoff,B Krag-Olsen,Claes Lundsteen	21
15	A familial balanced inverted insertion ins(15)(q15q13q11.2) producing Prader–Willi syndrome, Angelman syndrome and duplication of 15q11.2‐q13 in a single family: Importance of differentiation from a paracentric inversion 2004 ·American Journal of Medical Genetics Part A ·Morag N. Collinson,Siân E. Roberts,John A. Crolla,Nicholas R. Dennis	20
16	Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance. 1998 ·Journal of Medical Genetics ·John Barber,Christine A Joyce,Morag N. Collinson,James C. Nicholson,Lionel Willatt,(unknown),Mark S. Bateman,Andrew Green,John R.W. Yates,N R Dennis	53
17	Inv(10)(p11.2q21.2), a variant chromosome 1997 ·Human Genetics ·Morag N. Collinson,Andrew Fisher,(unknown),Jane Currie,Lisa M. Williams,Paul Roberts	23
18	Unbalanced translocation in a mother and her son in one of two 5;10 translocation families 1996 ·American Journal of Medical Genetics ·John Barber,I. Karen Temple,Paul L. Campbell,Morag N. Collinson,(unknown),(unknown),N R Dennis	15
19	Unbalanced translocation in a mother and her son in one of two 5;10 translocation families 1996 ·American Journal of Medical Genetics ·John Barber,I. Karen Temple,Paul L. Campbell,Morag N. Collinson,(unknown),(unknown),N R Dennis	1
20	The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27ß methylation analysis 1990 ·Genetics Research ·David Robinson,Yvonne Boyd,D.J. Cockburn,Morag N. Collinson,Ian Craig,Patricia A. Jacobs	20

About Morag N. Collinson

Morag N. Collinson is a scholar working on Genetics, Genetics and Pediatrics, Perinatology and Child Health, having authored 21 papers that have together received 473 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Genetics (381 citations), Pediatrics, Perinatology and Child Health (123 citations) and Molecular Biology (210 citations). Morag N. Collinson has collaborated with scholars based in United Kingdom, United States and Norway. Frequent co-authors include John Barber, John A. Crolla, Shuwen Huang, Patricia A. Jacobs, N R Dennis, Katherine Lachlan, Viv Maloney, N. Simon Thomas, Claire Turner and Mark S. Bateman. Their work appears in journals such as Journal of Medical Genetics, Human Genetics and Genetics in Medicine.

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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