M. Lance Cooper

2.1k total citations
19 papers, 838 citations indexed

About

M. Lance Cooper is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, M. Lance Cooper has authored 19 papers receiving a total of 838 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 9 papers in Plant Science and 7 papers in Molecular Biology. Recurrent topics in M. Lance Cooper's work include Genomic variations and chromosomal abnormalities (14 papers), Chromosomal and Genetic Variations (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). M. Lance Cooper is often cited by papers focused on Genomic variations and chromosomal abnormalities (14 papers), Chromosomal and Genetic Variations (9 papers) and Genetics and Neurodevelopmental Disorders (7 papers). M. Lance Cooper collaborates with scholars based in United States, Canada and Taiwan. M. Lance Cooper's co-authors include Sau Wai Cheung, Ankita Patel, Paweł Stankiewicz, A. Craig Chinault, Zhishuo Ou, Chad A. Shaw, James R. Lupski, Carlos A. Bacino, Svetlana A. Yatsenko and Arthur L. Beaudet and has published in prestigious journals such as PLoS ONE, PLoS Genetics and Genetics in Medicine.

In The Last Decade

M. Lance Cooper

19 papers receiving 781 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M. Lance Cooper United States 14 681 367 229 213 59 19 838
Leslie Domenici Kulikowski Brazil 15 487 0.7× 337 0.9× 174 0.8× 188 0.9× 69 1.2× 87 799
Liesbeth Rooms Belgium 17 593 0.9× 388 1.1× 133 0.6× 99 0.5× 27 0.5× 26 749
Karen Buysse Belgium 15 633 0.9× 456 1.2× 169 0.7× 75 0.4× 45 0.8× 19 959
Vanna Pecile Italy 17 499 0.7× 443 1.2× 175 0.8× 112 0.5× 70 1.2× 54 825
Marsha Speevak Canada 17 420 0.6× 302 0.8× 141 0.6× 96 0.5× 41 0.7× 37 636
A. Moncla France 17 748 1.1× 633 1.7× 174 0.8× 70 0.3× 97 1.6× 29 1.1k
Monika Cohen Germany 11 488 0.7× 551 1.5× 98 0.4× 84 0.4× 49 0.8× 13 859
J. Edward Spence United States 15 615 0.9× 527 1.4× 361 1.6× 82 0.4× 31 0.5× 23 959
R. Curtis Rogers United States 13 674 1.0× 492 1.3× 75 0.3× 69 0.3× 98 1.7× 20 882
Cristina Cuoco Italy 15 396 0.6× 275 0.7× 214 0.9× 89 0.4× 87 1.5× 38 647

Countries citing papers authored by M. Lance Cooper

Since Specialization
Citations

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

Fields of papers citing papers by M. Lance Cooper

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M. Lance Cooper. 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 M. Lance Cooper. The network helps show where M. Lance Cooper may publish in the future.

Co-authorship network of co-authors of M. Lance Cooper

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

All Works

19 of 19 papers shown
1.
Gu, Shen, Przemysław Szafrański, Zeynep Coban‐Akdemir, et al.. (2016). Mechanisms for Complex Chromosomal Insertions. PLoS Genetics. 12(11). e1006446–e1006446. 29 indexed citations
2.
Shinawi, Marwan, Mark P. Cain, Brian A. VanderBrink, et al.. (2010). Mixed gonadal dysgenesis in a child with isodicentric y chromosome: Does the relative proportion of the 45,X line really matter?. American Journal of Medical Genetics Part A. 152A(7). 1832–1837. 16 indexed citations
3.
Kang, Sung‐Hae, Chad A. Shaw, Zhishuo Ou, et al.. (2010). Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results. American Journal of Medical Genetics Part A. 152A(5). 1111–1126. 79 indexed citations
4.
Wiśniowiecka‐Kowalnik, Barbara, Sarika U. Peters, Zhilian Xia, et al.. (2010). Intragenic rearrangements in NRXN1 in three families with autism spectrum disorder, developmental delay, and speech delay. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(5). 983–993. 57 indexed citations
5.
Erez, Ayelet, Jessica Shu Nan Li, Michael T. Geraghty, et al.. (2010). Mosaic deletion 11p13 in a child with dopamine beta‐hydroxylase deficiency—Case report and review of the literature. American Journal of Medical Genetics Part A. 152A(3). 732–736. 10 indexed citations
6.
Ou, Zhishuo, Donna M. Martin, Jirair K. Bedoyan, et al.. (2008). Branchiootorenal syndrome and oculoauriculovertebral spectrum features associated with duplication ofSIX1,SIX6, andOTX2resulting from a complex chromosomal rearrangement. American Journal of Medical Genetics Part A. 146A(19). 2480–2489. 45 indexed citations
7.
Shchelochkov, Oleg A., M. Lance Cooper, Zhishuo Ou, et al.. (2008). Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement. Molecular Cytogenetics. 1(1). 16–16. 11 indexed citations
8.
Probst, Frank J., M. Lance Cooper, Sau Wai Cheung, & Monica J. Justice. (2008). Genotype, Phenotype, and Karyotype Correlation in the XO Mouse Model of Turner Syndrome. Journal of Heredity. 99(5). 512–517. 30 indexed citations
9.
Derwińska, Katarzyna, Marta Smyk, M. Lance Cooper, et al.. (2008). PTCH1 duplication in a family with microcephaly and mild developmental delay. European Journal of Human Genetics. 17(2). 267–271. 32 indexed citations
10.
Jiang, Yong‐hui, José E. Martínez, Zhishuo Ou, et al.. (2008). De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently “balanced” paracentric inversion of 14(q21q23). American Journal of Medical Genetics Part A. 146A(15). 1986–1993. 19 indexed citations
11.
Lu, Xinyan, Chad A. Shaw, Ankita Patel, et al.. (2007). Clinical Implementation of Chromosomal Microarray Analysis: Summary of 2513 Postnatal Cases. PLoS ONE. 2(3). e327–e327. 147 indexed citations
12.
Lennon, Patrick A., M. Lance Cooper, Daniel A. Peiffer, et al.. (2007). Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review. American Journal of Medical Genetics Part A. 143A(8). 791–798. 62 indexed citations
13.
Probst, Frank J., Elizabeth Roeder, Zhishuo Ou, et al.. (2007). Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation. American Journal of Medical Genetics Part A. 143A(12). 1358–1365. 44 indexed citations
14.
Powis, Zöe, Sung‐Hae Kang, M. Lance Cooper, et al.. (2007). Mosaic tetrasomy 12p with triplication of 12p detected by array‐based comparative genomic hybridization of peripheral blood DNA. American Journal of Medical Genetics Part A. 143A(24). 2910–2915. 15 indexed citations
15.
Cooper, M. Lance, et al.. (2006). A retrospective study of preimplantation embryos diagnosed with monosomy by fluorescence in situ hybridization (FISH). Cytogenetic and Genome Research. 114(3-4). 359–366. 9 indexed citations
16.
Lennon, Patrick A., M. Lance Cooper, Cynthia Lim, et al.. (2006). Array‐based comparative genomic hybridization facilitates identification of breakpoints of a novel der(1)t(1;18)(p36.3;q23)dn in a child presenting with mental retardation. American Journal of Medical Genetics Part A. 140A(11). 1156–1163. 3 indexed citations
17.
Cheung, Sau Wai, Chad A. Shaw, Wei Yu, et al.. (2005). Development and validation of a CGH microarray for clinical cytogenetic diagnosis. Genetics in Medicine. 7(6). 422–432. 185 indexed citations
18.
Scott, Daryl A., M. Lance Cooper, Paweł Stankiewicz, et al.. (2005). Congenital diaphragmatic hernia in WAGR syndrome. American Journal of Medical Genetics Part A. 134A(4). 430–433. 38 indexed citations
19.
Pearson, Margaret A., Paweł Stankiewicz, Patrick A. Lennon, et al.. (2005). Cryptic unbalanced translocation t(17;18)(p13.2;q22.3) identified by subtelomeric FISH and defined by array‐based comparative genomic hybridization in a patient with mental retardation and dysmorphic features. American Journal of Medical Genetics Part A. 137A(1). 88–93. 7 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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