Morag N. Collinson

2.2k total citations
21 papers, 473 citations indexed

About

Morag N. Collinson is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Morag N. Collinson has authored 21 papers receiving a total of 473 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 9 papers in Molecular Biology and 7 papers in Genetics. Recurrent topics in Morag N. Collinson's work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Morag N. Collinson is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). Morag N. Collinson collaborates with scholars based in United Kingdom, United States and Norway. Morag N. Collinson's co-authors include John Barber, John A. Crolla, Shuwen Huang, Patricia A. Jacobs, Katherine Lachlan, Viv Maloney, N. Simon Thomas, N R Dennis, Richard Sandford and Mark S. Bateman and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and Genetics in Medicine.

In The Last Decade

Morag N. Collinson

21 papers receiving 412 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Morag N. Collinson United Kingdom	14	381	210	123	97	32	21	473
Viv Maloney United Kingdom	14	453 1.2×	256 1.2×	119 1.0×	135 1.4×	57 1.8×	18	587
María Palomares‐Bralo Spain	13	364 1.0×	339 1.6×	105 0.9×	55 0.6×	28 0.9×	38	540
Joo Wook Ahn United Kingdom	13	424 1.1×	232 1.1×	159 1.3×	72 0.7×	34 1.1×	29	605
Paolo Guanciali Franchi Italy	14	298 0.8×	220 1.0×	80 0.7×	71 0.7×	54 1.7×	31	484
Sandra Peacock United States	9	308 0.8×	183 0.9×	207 1.7×	71 0.7×	15 0.5×	11	489
Rachel D. Burnside United States	11	460 1.2×	229 1.1×	173 1.4×	79 0.8×	29 0.9×	26	576
Roberto Coco Argentina	12	401 1.1×	213 1.0×	156 1.3×	143 1.5×	16 0.5×	45	531
Ko–ichiro Yoshiura Japan	12	251 0.7×	304 1.4×	107 0.9×	69 0.7×	31 1.0×	22	505
Sigrid Sahlén Sweden	11	327 0.9×	243 1.2×	115 0.9×	148 1.5×	26 0.8×	21	466
Eduardo S. Cantú United States	10	304 0.8×	288 1.4×	133 1.1×	39 0.4×	25 0.8×	18	499

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

Kharbanda, Mira, Mark S. Bateman, David Hunt, et al.. (2020). Directly Transmitted 12.3-Mb Deletion with a Consistent Phenotype in the Variable 11q21q22.3 Region. Cytogenetic and Genome Research. 160(4). 185–192. 1 indexed citations

Williams, Angharad, et al.. (2020). Exon-focused targeted oligonucleotide microarray design increases detection of clinically relevant variants across multiple NHS genomic centres. npj Genomic Medicine. 5(1). 28–28. 2 indexed citations

Tuke, Marcus A., Katherine S. Ruth, Andrew R. Wood, et al.. (2018). Mosaic Turner syndrome shows reduced penetrance in an adult population study. Genetics in Medicine. 21(4). 877–886. 86 indexed citations

Bateman, Mark S., Morag N. Collinson, David J. Bunyan, et al.. (2017). Incomplete penetrance, variable expressivity, or dosage insensitivity in four families with directly transmitted unbalanced chromosome abnormalities. American Journal of Medical Genetics Part A. 176(2). 319–329. 5 indexed citations

Wang, Rubin, Jonathan J. Waters, Christine Waterman, et al.. (2017). Inherited 2q23.1 microdeletions involving the MBD5 locus. Molecular Genetics & Genomic Medicine. 5(5). 608–613. 6 indexed citations

Salter, Claire, Diana Baralle, Morag N. Collinson, & Jay Self. (2016). 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. American Journal of Medical Genetics Part A. 170(4). 1017–1022. 5 indexed citations

Barber, John, Jill A. Rosenfeld, John M. Graham, et al.. (2015). Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significance. American Journal of Medical Genetics Part A. 167(9). 2052–2064. 28 indexed citations

Blyth, Moira, Viv Maloney, Sarah J. Beal, et al.. (2015). Pallister-Killian syndrome: a study of 22 British patients. Journal of Medical Genetics. 52(7). 454–464. 33 indexed citations

Willemsen, Marjolein H., Nicole de Leeuw, Catherine Mercer, et al.. (2010). Further molecular and clinical delineation of the Wisconsin syndrome phenotype associated with interstitial 3q24q25 deletions. American Journal of Medical Genetics Part A. 155(1). 106–112. 6 indexed citations

10.

Collinson, Morag N., Jocelyn Charlton, John A. Crolla, et al.. (2010). Symmetrical enchondromatosis is associated with duplication of 12p11.23 to 12p11.22 including PTHLH. American Journal of Medical Genetics Part A. 152A(12). 3124–3128. 17 indexed citations

11.

Tatton‐Brown, Katrina, Daniela T. Pilz, Karen Helene Ørstavik, et al.. (2009). 15q overgrowth syndrome: A newly recognized phenotype associated with overgrowth, learning difficulties, characteristic facial appearance, renal anomalies and increased dosage of distal chromosome 15q. American Journal of Medical Genetics Part A. 149A(2). 147–154. 55 indexed citations

12.

Balasubramanian, Meena, et al.. (2009). Inverted duplication of 1q32.1 to 1q44 characterized by array CGH and review of distal 1q partial trisomy. American Journal of Medical Genetics Part A. 149A(4). 793–797. 24 indexed citations

13.

Barber, John, N. Simon Thomas, Morag N. Collinson, et al.. (2004). Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences. European Journal of Human Genetics. 13(3). 283–291. 21 indexed citations

14.

Lachlan, Katherine, et al.. (2004). Functional disomy resulting from duplications of distal Xq in four unrelated patients. Human Genetics. 115(5). 399–408. 39 indexed citations

15.

Collinson, Morag N., Siân E. Roberts, John A. Crolla, & Nicholas R. Dennis. (2004). 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. American Journal of Medical Genetics Part A. 126A(1). 27–32. 20 indexed citations

16.

Barber, John, Christine A Joyce, Morag N. Collinson, et al.. (1998). Duplication of 8p23.1: a cytogenetic anomaly with no established clinical significance.. Journal of Medical Genetics. 35(6). 491–496. 53 indexed citations

17.

Collinson, Morag N., et al.. (1997). Inv(10)(p11.2q21.2), a variant chromosome. Human Genetics. 101(2). 175–180. 23 indexed citations

18.

Barber, John, et al.. (1996). Unbalanced translocation in a mother and her son in one of two 5;10 translocation families. American Journal of Medical Genetics. 62(1). 84–90. 15 indexed citations

19.

Barber, John, et al.. (1996). Unbalanced translocation in a mother and her son in one of two 5;10 translocation families. American Journal of Medical Genetics. 62(1). 84–90. 1 indexed citations

20.

Robinson, David, Yvonne Boyd, D.J. Cockburn, et al.. (1990). The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27ß methylation analysis. Genetics Research. 56(2-3). 135–140. 20 indexed citations

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