Philip D. Cotter

3.7k total citations
95 papers, 2.4k citations indexed

About

Philip D. Cotter is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Philip D. Cotter has authored 95 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 44 papers in Molecular Biology and 35 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Philip D. Cotter's work include Genomic variations and chromosomal abnormalities (45 papers), Prenatal Screening and Diagnostics (31 papers) and Chromosomal and Genetic Variations (23 papers). Philip D. Cotter is often cited by papers focused on Genomic variations and chromosomal abnormalities (45 papers), Prenatal Screening and Diagnostics (31 papers) and Chromosomal and Genetic Variations (23 papers). Philip D. Cotter collaborates with scholars based in United States, United Kingdom and New Zealand. Philip D. Cotter's co-authors include David F. Bishop, Katherine A. Rauen, Marc Baumann, Kurt Hirschhorn, Daniel Pinkel, William E. Tidyman, Michael A. Teitell, Anne L. Estep, Alison May and Donna G. Albertson and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Journal of Clinical Oncology.

In The Last Decade

Philip D. Cotter

91 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Philip D. Cotter United States 26 1.3k 994 538 318 298 95 2.4k
Barbara K. Goodman United States 25 811 0.6× 360 0.4× 124 0.2× 109 0.3× 146 0.5× 48 1.5k
Mirella Filocamo Italy 34 1.9k 1.4× 431 0.4× 153 0.3× 45 0.1× 138 0.5× 158 4.3k
Shaun S. Abeysinghe United Kingdom 8 1.4k 1.1× 845 0.9× 57 0.1× 185 0.6× 186 0.6× 8 2.1k
Irene Newsham United States 29 1.5k 1.2× 628 0.6× 105 0.2× 49 0.2× 469 1.6× 44 2.8k
Marjolein Kriek Netherlands 19 773 0.6× 607 0.6× 131 0.2× 89 0.3× 86 0.3× 31 1.4k
Quinten Waisfisz Netherlands 36 4.4k 3.3× 1.5k 1.6× 145 0.3× 469 1.5× 1.4k 4.7× 89 5.5k
Berivan Baskin Canada 25 1.1k 0.9× 470 0.5× 107 0.2× 37 0.1× 197 0.7× 47 2.1k
Gail Chuck United States 20 1.3k 1.0× 290 0.3× 69 0.1× 705 2.2× 76 0.3× 36 3.0k
Michael Zeschnigk Germany 30 2.2k 1.6× 731 0.7× 271 0.5× 39 0.1× 294 1.0× 72 3.3k
Elke Holinski‐Feder Germany 33 1.5k 1.2× 934 0.9× 110 0.2× 57 0.2× 923 3.1× 127 3.7k

Countries citing papers authored by Philip D. Cotter

Since Specialization
Citations

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

Fields of papers citing papers by Philip D. Cotter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philip D. Cotter. 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 Philip D. Cotter. The network helps show where Philip D. Cotter may publish in the future.

Co-authorship network of co-authors of Philip D. Cotter

This figure shows the co-authorship network connecting the top 25 collaborators of Philip D. Cotter. A scholar is included among the top collaborators of Philip D. Cotter 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 Philip D. Cotter. Philip D. Cotter 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
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Kovaleva, Natalia & Philip D. Cotter. (2016). Somatic/gonadal mosaicism for structural autosomal rearrangements: female predominance among carriers of gonadal mosaicism for unbalanced rearrangements. Molecular Cytogenetics. 9(1). 8–8. 19 indexed citations
4.
Golabi, Mahin, et al.. (2009). Gardner‐Silengo‐Wachtel or genito‐palato‐cadiac syndrome with associated autosomal aneuploidy. American Journal of Medical Genetics Part A. 149A(4). 693–697. 1 indexed citations
5.
Thompson, Paul M., Philip D. Cotter, John McNaught, et al.. (2008). Building a Bio-Event Annotated Corpus for the Acquisition of Semantic Frames from Biomedical Corpora. Language Resources and Evaluation. 2159–2166. 8 indexed citations
6.
Ananiadou, Sophia, Philip D. Cotter, Chikashi Nobata, et al.. (2007). SemText: A semantically enriched information retrieval system for biology. Research Explorer (The University of Manchester). 1 indexed citations
7.
Glass, Ian A., Katherine A. Rauen, Emily Chen, et al.. (2005). Ring chromosome 15: characterization by array CGH. Human Genetics. 118(5). 611–617. 41 indexed citations
8.
Klein, Ophir D., Philip D. Cotter, Ann Marie Schmidt, et al.. (2005). Interstitial deletion of chromosome 12q: Genotype–phenotype correlation of two patients utilizing array comparative genomic hybridization. American Journal of Medical Genetics Part A. 138A(4). 349–354. 12 indexed citations
9.
Iglesias, Alejandro, Katherine A. Rauen, Donna G. Albertson, Daniel Pinkel, & Philip D. Cotter. (2005). Duplication of distal 20q: clinical, cytogenetic and array CGH Characterization of a new case. Clinical Dysmorphology. 15(1). 19–23. 6 indexed citations
10.
Rauen, Katherine A., Mahin Golabi, & Philip D. Cotter. (2003). Fertility in a female with mosaic trisomy 8. Fertility and Sterility. 79(1). 206–208. 18 indexed citations
11.
Kostiner, Dana, et al.. (2002). Stabilization of a terminal inversion duplication of 8p by telomere capture from 18q. Cytogenetic and Genome Research. 98(1). 9–12. 20 indexed citations
12.
Lammer, Edward J., et al.. (2001). Inherited duplication of Xq27.2 ??? qter: phenocopy of infantile Prader-Willi syndrome. Clinical Dysmorphology. 10(2). 141–144. 23 indexed citations
13.
Glass, Ian A., Adrian Trenholme, Lindsay Mildenhall, Richard J. Bailey, & Philip D. Cotter. (2000). Mild phenotype in two siblings with distal monosomy 12p13.31→pter. Clinical Genetics. 57(5). 401–405. 12 indexed citations
14.
McGhee, Eva, et al.. (2000). Monosomy 16 as the Sole Abnormality in Myeloid Malignancies. Cancer Genetics and Cytogenetics. 118(2). 163–166. 6 indexed citations
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Wright, Tracy J., Darrell Ricke, Philip D. Cotter, et al.. (1997). A Transcript Map of the Newly Defined 165 kb Wolf-Hirschhorn Syndrome Critical Region. Human Molecular Genetics. 6(2). 317–324. 169 indexed citations
17.
Cotter, Philip D., et al.. (1997). Paternal uniparental disomy for chromosome 14: A case report and review. American Journal of Medical Genetics. 70(1). 74–79. 83 indexed citations
18.
Cotter, Philip D., et al.. (1997). Screening for the mitochondrial DNA A3243G mutation in children with insulin-dependent diabetes mellitus. Metabolism. 46(4). 445–449. 6 indexed citations
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Cotter, Philip D., Huntington F. Willard, Jerome L. Gorski, & David F. Bishop. (1992). Assignment of human erythroid δ-aminolevulinate synthase (ALAS2) to a distal subregion of band Xp11.21 by PCR analysis of somatic cell hybrids containing X;Autosome translocations. Genomics. 13(1). 211–212. 52 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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