Mary C. Phelan

3.6k total citations
68 papers, 2.4k citations indexed

About

Mary C. Phelan is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Mary C. Phelan has authored 68 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 31 papers in Molecular Biology and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Mary C. Phelan's work include Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (13 papers) and Viral Infectious Diseases and Gene Expression in Insects (9 papers). Mary C. Phelan is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Prenatal Screening and Diagnostics (13 papers) and Viral Infectious Diseases and Gene Expression in Insects (9 papers). Mary C. Phelan collaborates with scholars based in United States, United Kingdom and Switzerland. Mary C. Phelan's co-authors include Roger E. Stevenson, Ron C. Michaelis, Richard J. Schroer, Eric Crawford, Steven A. Skinner, R. Curtis Rogers, Robert A. Saul, Cindy Skinner, Richard J. Simensen and Jack Tarleton and has published in prestigious journals such as Nature, New England Journal of Medicine and PEDIATRICS.

In The Last Decade

Mary C. Phelan

68 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
Mary C. Phelan United States 25 1.4k 1.0k 480 415 367 68 2.4k
J Boué France 22 1.5k 1.1× 1.4k 1.4× 583 1.2× 377 0.9× 175 0.5× 82 2.6k
Jürgen Horst Germany 27 1.1k 0.8× 1.7k 1.6× 205 0.4× 330 0.8× 146 0.4× 74 2.9k
Howard R. Slater Australia 32 1.8k 1.2× 1.3k 1.3× 452 0.9× 795 1.9× 390 1.1× 99 3.0k
Rolph Pfundt Netherlands 42 2.9k 2.0× 2.6k 2.5× 223 0.5× 586 1.4× 190 0.5× 136 5.2k
Amy M. Breman United States 20 713 0.5× 587 0.6× 119 0.2× 502 1.2× 139 0.4× 47 1.4k
Lucy R. Osborne Canada 32 931 0.6× 1.3k 1.2× 182 0.4× 136 0.3× 163 0.4× 69 3.1k
Heon Yung Gee South Korea 31 691 0.5× 1.5k 1.5× 366 0.8× 178 0.4× 163 0.4× 108 3.0k
Alan Packer United States 17 975 0.7× 1.4k 1.4× 592 1.2× 77 0.2× 84 0.2× 25 2.4k
Jo Peters United Kingdom 31 2.0k 1.4× 2.6k 2.5× 121 0.3× 537 1.3× 258 0.7× 66 3.8k
Barbara F. Crandall United States 25 719 0.5× 704 0.7× 48 0.1× 740 1.8× 245 0.7× 88 2.0k

Countries citing papers authored by Mary C. Phelan

Since Specialization
Citations

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

Fields of papers citing papers by Mary C. Phelan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mary C. Phelan. 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 Mary C. Phelan. The network helps show where Mary C. Phelan may publish in the future.

Co-authorship network of co-authors of Mary C. Phelan

This figure shows the co-authorship network connecting the top 25 collaborators of Mary C. Phelan. A scholar is included among the top collaborators of Mary C. Phelan 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 Mary C. Phelan. Mary C. Phelan 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.
Fuerst‐Waltl, Birgit, Hermann Schwarzenbacher, C. Egger-Danner, et al.. (2023). The Combined Use of Automated Milking System and Sensor Data to Improve Detection of Mild Lameness in Dairy Cattle. Animals. 13(7). 1180–1180. 15 indexed citations
2.
Phelan, Mary C., Judith Anzures‐Cabrera, David Carlile, et al.. (2013). Effect of Hepatic and Renal Impairment on the Pharmacokinetics of Dalcetrapib. Clinical Pharmacokinetics. 52(4). 255–265. 10 indexed citations
3.
Derks, Michael, et al.. (2011). Safety, Tolerability and Pharmacokinetics of Dalcetrapib Following Single and Multiple Ascending Doses in Healthy Subjects. Clinical Drug Investigation. 31(5). 325–335. 17 indexed citations
4.
Derks, Michael, et al.. (2010). No clinically relevant drug–drug interactions when dalcetrapib is co-administered with atorvastatin. Expert Opinion on Investigational Drugs. 19(10). 1135–1145. 18 indexed citations
5.
Derks, Michael, Markus Abt, & Mary C. Phelan. (2010). Lack of clinically relevant drug–drug interactions when dalcetrapib is co‐administered with ezetimibe. British Journal of Clinical Pharmacology. 70(6). 825–833. 12 indexed citations
6.
Derks, Michael, et al.. (2010). Coadministration of Dalcetrapib With Pravastatin, Rosuvastatin, or Simvastatin: No Clinically Relevant Drug‐Drug Interactions. The Journal of Clinical Pharmacology. 50(10). 1188–1201. 22 indexed citations
7.
Phelan, Mary C.. (2007). Techniques for Mammalian Cell Tissue Culture. Current Protocols in Toxicology. 33(1). 9 indexed citations
8.
Phelan, Mary C., et al.. (2001). Prenatal diagnosis of mosaicism for triploidy and trisomy 13. Prenatal Diagnosis. 21(6). 457–460. 5 indexed citations
9.
Michaelis, Ron C., et al.. (2001). Microsatellite analysis reveals a high incidence of maternal cell contamination in 46,XX products of conception consisting of villi or a combination of villi and membranous material. American Journal of Obstetrics and Gynecology. 185(1). 198–203. 28 indexed citations
10.
Phelan, Mary C., et al.. (1998). Vascular anastomoses leading to amelia and cutis aplasia in a dizygotic twin pregnancy. Clinical Genetics. 53(2). 126–130. 14 indexed citations
11.
Willi, Steven M., et al.. (1997). A Deletion in the Long Arm of Chromosome 18 in a Child with Serum Carnosinase Deficiency1. Pediatric Research. 41(2). 210–213. 29 indexed citations
12.
Phelan, Mary C.. (1996). Techniques for Mammalian Cell Tissue Culture. Current Protocols in Molecular Biology. 35(1). 2 indexed citations
13.
Phelan, Mary C., et al.. (1995). Prenatal diagnosis of mosaic 4p – in a fetus with trisomy 21. Prenatal Diagnosis. 15(3). 274–277. 3 indexed citations
14.
Pettenati, Mark J., P. Nagesh Rao, Mary C. Phelan, et al.. (1995). Paracentric inversions in humans: A review of 446 paracentric inversions with presentation of 120 new cases. American Journal of Medical Genetics. 55(2). 171–187. 82 indexed citations
15.
Michaelis, Ron C., Steven A. Skinner, Richard J. Simensen, et al.. (1995). Deletion involving D15S113 in a mother and son without Angelman syndrome: Refinement of the Angelman syndrome critical deletion region. American Journal of Medical Genetics. 55(1). 120–126. 9 indexed citations
16.
McConkie‐Rosell, Allyn, Ave M. Lachiewicz, Gail A. Spiridigliozzi, et al.. (1993). Evidence that methylation of the FMR-I locus is responsible for variable phenotypic expression of the fragile X syndrome.. PubMed. 53(4). 800–9. 138 indexed citations
17.
Phelan, Mary C., Gordon R. Thomas, Robert A. Saul, et al.. (1992). Cytogenetic, biochemical, and molecular analyses of a 22q13 deletion. American Journal of Medical Genetics. 43(5). 872–876. 42 indexed citations
18.
Phelan, Mary C., et al.. (1988). Fragile X syndrome and neoplasia. American Journal of Medical Genetics. 30(1-2). 77–82. 22 indexed citations
19.
Schwartz, Charles E., Mary C. Phelan, P. N. Howard‐Peebles, et al.. (1988). Fragile X syndrome: Linkage analysis in black and white populations. American Journal of Medical Genetics. 30(1-2). 531–542. 5 indexed citations
20.
Phelan, Mary C., John M. Pellock, & Walter E. Nance. (1983). Discordant Expression of Fetal Hydantoin Syndrome in Heteropaternal Dizygotic Twins. Obstetrical & Gynecological Survey. 38(5). 277–279. 2 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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