Mark S. Bateman

1.1k total citations
12 papers, 193 citations indexed

About

Mark S. Bateman is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Mark S. Bateman has authored 12 papers receiving a total of 193 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 9 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Mark S. Bateman's work include Genomic variations and chromosomal abnormalities (10 papers), Congenital Ear and Nasal Anomalies (5 papers) and Congenital heart defects research (5 papers). Mark S. Bateman is often cited by papers focused on Genomic variations and chromosomal abnormalities (10 papers), Congenital Ear and Nasal Anomalies (5 papers) and Congenital heart defects research (5 papers). Mark S. Bateman collaborates with scholars based in United Kingdom, United States and Norway. Mark S. Bateman's co-authors include John Barber, Lionel Willatt, Morag N. Collinson, Shuwen Huang, James C. Nicholson, Christine A Joyce, N R Dennis, Viv Maloney, Andrew Green and John R.W. Yates and has published in prestigious journals such as Atherosclerosis, Journal of Medical Genetics and Clinical Endocrinology.

In The Last Decade

Mark S. Bateman

12 papers receiving 160 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mark S. Bateman United Kingdom	6	156	86	60	49	20	12	193
M.L. Martínez‐Fernández Spain	9	154 1.0×	78 0.9×	58 1.0×	48 1.0×	14 0.7×	20	196
V.K. Maloney United Kingdom	9	263 1.7×	174 2.0×	54 0.9×	46 0.9×	8 0.4×	12	304
Carla S. D’Angelo Brazil	10	229 1.5×	156 1.8×	27 0.5×	42 0.9×	14 0.7×	15	302
Olga Žilina Estonia	12	242 1.6×	132 1.5×	54 0.9×	92 1.9×	8 0.4×	23	314
Amelia Villa Spain	9	176 1.1×	83 1.0×	50 0.8×	75 1.5×	21 1.1×	12	241
Christine A Joyce United Kingdom	8	195 1.3×	145 1.7×	68 1.1×	98 2.0×	12 0.6×	10	255
Gordon S. Stephen United Kingdom	8	171 1.1×	100 1.2×	62 1.0×	66 1.3×	13 0.7×	15	239
N. P. Carter United Kingdom	5	180 1.2×	128 1.5×	76 1.3×	25 0.5×	8 0.4×	5	242
Annice Hill United States	7	212 1.4×	108 1.3×	49 0.8×	69 1.4×	16 0.8×	10	253

Countries citing papers authored by Mark S. Bateman

Since Specialization

Citations

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

Fields of papers citing papers by Mark S. Bateman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mark S. Bateman. 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 Mark S. Bateman. The network helps show where Mark S. Bateman may publish in the future.

Co-authorship network of co-authors of Mark S. Bateman

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

All Works

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12 of 12 papers shown

Sakka, Sophia, Kathy Mann, Katherine Lachlan, et al.. (2020). Haematological chimerism masquerading as disorder of sex development. Clinical Endocrinology. 92(5). 487–489. 1 indexed citations

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

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

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

Barber, John, Jill A. Rosenfeld, Nicola Foulds, et al.. (2013). 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients. American Journal of Medical Genetics Part A. 161(3). 487–500. 33 indexed citations

Barber, John, et al.. (2013). Another Family with a Euchromatic Duplication Variant of 9q13-q21.1 Derived from Segmentally Duplicated Pericentromeric Euchromatin. Cytogenetic and Genome Research. 141(1). 64–69. 3 indexed citations

Barber, John, Charlotte Brasch‐Andersen, V.K. Maloney, et al.. (2012). A Novel Pseudo-Dicentric Variant of 16p11.2–q11.2 Contains Euchromatin from 16p11.2–p11.1 and Resembles Pathogenic Duplications of Proximal 16q. Cytogenetic and Genome Research. 139(1). 59–64. 3 indexed citations

Barber, John, Victoria L. Hall, Viv Maloney, et al.. (2012). 16p11.2–p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2. European Journal of Human Genetics. 21(2). 182–189. 34 indexed citations

Barber, John, Shuwen Huang, Mark S. Bateman, & Amanda Collins. (2011). Transmitted deletions of medial 5p and learning difficulties; Does the cadherin cluster only become penetrant when flanking genes are deleted?. American Journal of Medical Genetics Part A. 155(11). 2807–2815. 6 indexed citations

10.

Bateman, Mark S., Sarju Mehta, Lionel Willatt, et al.. (2010). A de novo 4q34 interstitial deletion of at least 9.3 Mb with no discernible phenotypic effect. American Journal of Medical Genetics Part A. 152A(7). 1764–1769. 25 indexed citations

11.

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

12.

Marais, A. David, et al.. (1994). Atorvastatin is a powerful and safe agent for lowering plasma cholesterol concentration in heterozygous familial hypercholesterolemia. Atherosclerosis. 109(1-2). 316–316. 1 indexed citations

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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