Andrew Norman

2.8k total citations
30 papers, 825 citations indexed

About

Andrew Norman is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Andrew Norman has authored 30 papers receiving a total of 825 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 11 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Andrew Norman's work include Muscle Physiology and Disorders (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Prenatal Screening and Diagnostics (7 papers). Andrew Norman is often cited by papers focused on Muscle Physiology and Disorders (8 papers), Genomic variations and chromosomal abnormalities (8 papers) and Prenatal Screening and Diagnostics (7 papers). Andrew Norman collaborates with scholars based in United Kingdom, South Africa and United States. Andrew Norman's co-authors include Peter S. Harper, Dian Donnai, Andrew Read, D. Gareth Evans, Richard W. Whitehousé, Eamonn R. Maher, Susan Huson, David Thrush, Anthony Moran and M Super and has published in prestigious journals such as The Lancet, Human Molecular Genetics and BMC Genomics.

In The Last Decade

Andrew Norman

29 papers receiving 787 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew Norman United Kingdom 17 444 211 160 122 110 30 825
Yvonne J. Vos Netherlands 19 520 1.2× 240 1.1× 80 0.5× 103 0.8× 111 1.0× 42 1.0k
Cecilia Bondjers Sweden 11 838 1.9× 181 0.9× 171 1.1× 111 0.9× 124 1.1× 11 1.3k
A.M.W. van den Ouweland Netherlands 17 327 0.7× 422 2.0× 201 1.3× 58 0.5× 41 0.4× 27 1.0k
Fuzi Jin United States 11 756 1.7× 199 0.9× 63 0.4× 134 1.1× 76 0.7× 19 1.0k
Zunyi Zhang China 22 847 1.9× 217 1.0× 260 1.6× 116 1.0× 67 0.6× 58 1.3k
Lauren Massingham United States 8 365 0.8× 295 1.4× 90 0.6× 57 0.5× 50 0.5× 19 845
Jasmin Jacob–Hirsch Israel 13 570 1.3× 79 0.4× 114 0.7× 114 0.9× 137 1.2× 15 1.1k
Annick Francis Belgium 11 496 1.1× 125 0.6× 78 0.5× 153 1.3× 106 1.0× 16 800
Anju Shukla India 18 610 1.4× 496 2.4× 78 0.5× 89 0.7× 106 1.0× 112 1.2k
M. Marin-Padilla United States 15 930 2.1× 261 1.2× 107 0.7× 105 0.9× 320 2.9× 24 1.6k

Countries citing papers authored by Andrew Norman

Since Specialization
Citations

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

Fields of papers citing papers by Andrew Norman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Andrew Norman

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

All Works

20 of 20 papers shown
1.
Low, Karen, Karen Stals, Richard Caswell, et al.. (2018). Phenotype of CNTNAP1: a study of patients demonstrating a specific severe congenital hypomyelinating neuropathy with survival beyond infancy. European Journal of Human Genetics. 26(6). 796–807. 18 indexed citations
2.
Meyer, Esther, Manju A. Kurian, Neil V. Morgan, et al.. (2011). Promoter mutation is a common variant in GJC2-associated Pelizaeus–Merzbacher-like disease. Molecular Genetics and Metabolism. 104(4). 637–643. 18 indexed citations
3.
Fullston, Tod, Merran Finnis, Anna Hackett, et al.. (2011). Screening and cell-based assessment of mutations in the Aristaless-related homeobox (ARX) gene. Clinical Genetics. 80(6). 510–522. 16 indexed citations
4.
Hearle, Nicholas, Ian Tomlinson, Wendy Lim, et al.. (2005). Sequence changes in predicted promoter elements of STK11/LKB1 are unlikely to contribute to Peutz-Jeghers syndrome. BMC Genomics. 6(1). 38–38. 11 indexed citations
5.
Hérasse, Muriel, Zuzana Dobbie, Dieter Gläser, et al.. (2003). Severe hypophosphatasia: Characterization of fifteen novel mutations in the ALPL gene. Human Mutation. 22(1). 105–106. 26 indexed citations
6.
Thrush, David, et al.. (2002). Radiation-induced brachial plexopathy in women treated for carcinoma of the breast. Clinical Rehabilitation. 16(2). 160–165. 62 indexed citations
7.
Tassabehji, Mayada, Valerie Newton, Angela F. Brady, et al.. (1995). The mutational spectrum in Waardenburg syndrome. Human Molecular Genetics. 4(11). 2131–2137. 172 indexed citations
8.
Prasher, V. P., et al.. (1995). Partial trisomy 22 (q11.2-q13.1) as a result of duplication and pericentric inversion.. Journal of Medical Genetics. 32(4). 306–308. 16 indexed citations
9.
Norman, Andrew, et al.. (1994). Examination of fetuses after induced abortion for fetal abnormality—a follow‐up study. Prenatal Diagnosis. 14(5). 381–385. 16 indexed citations
10.
Davies, D. Rhodri, Andrew Norman, Richard W. Whitehousé, & D. Gareth Evans. (1994). Non‐expression of von Hippel‐Lindau phenotype in an obligate gene carrier. Clinical Genetics. 45(2). 104–106. 6 indexed citations
11.
Norman, Andrew, et al.. (1993). True telomeric translocation in a baby with the Prader‐Willi phenotype. American Journal of Medical Genetics. 47(1). 1–6. 19 indexed citations
12.
Norman, Andrew & Dian Donnai. (1992). Hypoplastic thumbs and hydranencephaly. Clinical Dysmorphology. 1(2). 121–121. 3 indexed citations
13.
Norman, Andrew, et al.. (1992). De novo inverted duplication of chromosome 7q. Journal of Medical Genetics. 29(11). 837–838. 8 indexed citations
14.
Norman, Andrew, Andrew Read, Jill Clayton‐Smith, Tony Andrews, & Dian Donnai. (1992). Recurrent Wiedemann‐Beckwith syndrome with inversion of chromosome (11)(p11.2p15.5). American Journal of Medical Genetics. 42(4). 638–641. 46 indexed citations
15.
Norman, Andrew, S. Rimmer, Sara Landy, & D Donnai. (1992). Thanatophoric dysplasia of the straight-bone type (type 2). Clinical Dysmorphology. 1(2). 115???120–115???120. 17 indexed citations
16.
Upadhyaya, Meena, Robert A. Smith, N S Thomas, Andrew Norman, & P.S. Harper. (1990). Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA. Clinical Genetics. 37(6). 456–462. 15 indexed citations
17.
Norman, Andrew, J. H. Coakley, Nick Thomas, & Peter S. Harper. (1989). DISTINCTION OF BECKER FROM LIMB-GIRDLE MUSCULAR DYSTROPHY BY MEANS OF DYSTROPHIN cDNA PROBES. The Lancet. 333(8636). 466–468. 46 indexed citations
18.
Norman, Andrew, Christopher Rogers, J R Sibert, & P.S. Harper. (1989). Duchenne muscular dystrophy in Wales: a 15 year study, 1971 to 1986.. Journal of Medical Genetics. 26(9). 560–564. 7 indexed citations
19.
Norman, Andrew, et al.. (1989). Dystrophin analysis in the diagnosis of muscular dystrophy.. Archives of Disease in Childhood. 64(10). 1501–1503. 7 indexed citations
20.
Norman, Andrew & Peter S. Harper. (1989). A survey of manifesting carriers of Duchenne and Becker muscular dystrophy in Wales. Clinical Genetics. 36(1). 31–37. 45 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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