Christopher McCaskill

1.7k total citations
22 papers, 825 citations indexed

About

Christopher McCaskill is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Christopher McCaskill has authored 22 papers receiving a total of 825 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Genetics, 15 papers in Pediatrics, Perinatology and Child Health and 5 papers in Molecular Biology. Recurrent topics in Christopher McCaskill's work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (14 papers) and Genetic Syndromes and Imprinting (11 papers). Christopher McCaskill is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (14 papers) and Genetic Syndromes and Imprinting (11 papers). Christopher McCaskill collaborates with scholars based in United States, Netherlands and Mexico. Christopher McCaskill's co-authors include Lisa G. Shaffer, Sue Ann Berend, Frank Greenberg, V. Reid Sutton, Aimee S. Spikes, F.F.B. Elder, Stuart K. Shapira, Hope Northrup, Julie R. Korenberg and Lorraine Potocki and has published in prestigious journals such as The American Journal of Human Genetics, Human Genetics and American Journal of Medical Genetics.

In The Last Decade

Christopher McCaskill

21 papers receiving 720 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christopher McCaskill United States 16 672 397 296 127 42 22 825
C Baccichetti Italy 14 539 0.8× 204 0.5× 287 1.0× 207 1.6× 54 1.3× 32 686
Azzedine Aboura France 17 525 0.8× 258 0.6× 311 1.1× 110 0.9× 41 1.0× 40 767
Amber N. Pursley United States 20 1.1k 1.6× 690 1.7× 498 1.7× 250 2.0× 61 1.5× 28 1.4k
Carolina Sismani Cyprus 19 735 1.1× 266 0.7× 515 1.7× 184 1.4× 38 0.9× 75 984
Courtney Sebold United States 16 437 0.7× 141 0.4× 216 0.7× 97 0.8× 52 1.2× 27 616
Elke Back Germany 15 576 0.9× 138 0.3× 456 1.5× 247 1.9× 41 1.0× 36 829
Cristina Cuoco Italy 15 396 0.6× 214 0.5× 275 0.9× 89 0.7× 87 2.1× 38 647
Alicia Delicado Spain 16 459 0.7× 201 0.5× 340 1.1× 102 0.8× 129 3.1× 47 706
J Lejeune France 14 328 0.5× 163 0.4× 202 0.7× 99 0.8× 35 0.8× 50 576
J. O. Van Hemel Netherlands 21 809 1.2× 356 0.9× 457 1.5× 193 1.5× 109 2.6× 38 1.1k

Countries citing papers authored by Christopher McCaskill

Since Specialization
Citations

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

Fields of papers citing papers by Christopher McCaskill

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christopher McCaskill

This figure shows the co-authorship network connecting the top 25 collaborators of Christopher McCaskill. A scholar is included among the top collaborators of Christopher McCaskill 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 Christopher McCaskill. Christopher McCaskill 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.
Berend, Sue Ann, Scott L. Page, William Walker Atkinson, et al.. (2003). Obligate Short-Arm Exchange in De Novo Robertsonian Translocation Formation Influences Placement of Crossovers in Chromosome 21 Nondisjunction. The American Journal of Human Genetics. 72(2). 488–495. 7 indexed citations
2.
Heller, Anita, et al.. (2002). Parental Origin and Timing of De Novo Robertsonian Translocation Formation. The American Journal of Human Genetics. 71(6). 1456–1462. 67 indexed citations
3.
McCaskill, Christopher, et al.. (2002). Mosaicism in a patient with Down syndrome reveals post‐fertilization formation of a robertsonian translocation and isochromosome. American Journal of Medical Genetics Part A. 116A(2). 159–163. 31 indexed citations
4.
Berend, Sue Ann, Bassem A. Bejjani, Christopher McCaskill, & Lisa G. Shaffer. (2002). Identification of uniparental disomy in phenotypically abnormal carriers of isochromosomes or Robertsonian translocations. American Journal of Medical Genetics. 111(4). 362–365. 28 indexed citations
5.
Berend, Sue Ann, et al.. (2002). The importance of investigating for uniparental disomy in prenatally identified balanced acrocentric rearrangements. Prenatal Diagnosis. 22(2). 141–143. 2 indexed citations
6.
Wu, Yuanqing, José L. Badano, Christopher McCaskill, et al.. (2000). Haploinsufficiency of ALX4 as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene–Deletion Syndrome. The American Journal of Human Genetics. 67(5). 1327–1332. 65 indexed citations
7.
Berend, Sue Ann, et al.. (2000). Identification of Uniparental Disomy Following Prenatal Detection of Robertsonian Translocations and Isochromosomes. The American Journal of Human Genetics. 66(6). 1787–1793. 73 indexed citations
8.
Wu, Yuanqing, José L. Badano, Christopher McCaskill, et al.. (2000). Haploinsufficiency ofALX4as a Potential Cause of Parietal Foramina in the 11p11.2 Contiguous Gene–Deletion Syndrome. The American Journal of Human Genetics. 67(5). 1327–1332. 22 indexed citations
9.
Berend, Sue Ann, et al.. (1999). Investigation of two cases of paternal disomy 13 suggests timing of isochromosome formation and mechanisms leading to uniparental disomy. American Journal of Medical Genetics. 82(3). 275–281. 40 indexed citations
10.
Berend, Sue Ann, et al.. (1998). Molecular analysis of mosaicism for two different de novo acrocentric rearrangements demonstrates diversity in Robertsonian translocation formation. American Journal of Medical Genetics. 80(3). 252–259. 17 indexed citations
11.
Shaffer, Lisa G., et al.. (1998). Systematic search for uniparental disomy in early fetal losses: The results and a review of the literature. American Journal of Medical Genetics. 79(5). 366–372. 43 indexed citations
12.
Shaffer, Lisa G., et al.. (1998). Systematic search for uniparental disomy in early fetal losses: The results and a review of the literature. American Journal of Medical Genetics. 79(5). 366–372. 4 indexed citations
13.
Shaffer, Lisa G., Christopher McCaskill, CATHERINE A. EGLI, John C. Baker, & Kathreen Johnston. (1997). Is There an Abnormal Phenotype Associated with Maternal Isodisomy for Chromosome 2 in the Presence of Two Isochromosomes?. The American Journal of Human Genetics. 61(2). 461–462. 2 indexed citations
14.
Shapira, Stuart K., Christopher McCaskill, Hope Northrup, et al.. (1997). Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome. The American Journal of Human Genetics. 61(3). 642–650. 201 indexed citations
15.
McCaskill, Christopher, et al.. (1996). A clinical and molecular study of mosaicism for trisomy 17. Human Genetics. 97(1). 69–72. 33 indexed citations
16.
Walter, Christi A., Lisa G. Shaffer, Celia I. Kaye, et al.. (1996). Short-limb dwarfism and hypertrophic cardiomyopathy in a patient with paternal isodisomy 14: 45,XY,idic(14)(p11). American Journal of Medical Genetics. 65(4). 259–265. 50 indexed citations
17.
Schneider, Adele, et al.. (1996). Comprehensive 4-year follow-up on a case of maternal heterodisomy for chromosome 16. American Journal of Medical Genetics. 66(2). 204–208. 22 indexed citations
18.
Booth, Carol, et al.. (1995). Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism. Prenatal Diagnosis. 15(9). 843–848. 36 indexed citations
19.
Veyver, Ignatia B. Van den, Michelle Macha, Christopher McCaskill, Robert J. Carpenter, & Lisa G. Shaffer. (1993). Prenatal diagnosis and clinical findings in a case of hexasomy 12p. American Journal of Medical Genetics. 47(8). 1171–1174. 9 indexed citations
20.
Shaffer, Lisa G., et al.. (1993). Further characterization of 19 cases of rea(21q21q) and delineation as isochromosomes or robertsonian translocations in down syndrome. American Journal of Medical Genetics. 47(8). 1218–1222. 42 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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