Margaret J. McMillin

3.2k total citations
6 papers, 286 citations indexed

About

Margaret J. McMillin is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Margaret J. McMillin has authored 6 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Margaret J. McMillin's work include Genomics and Rare Diseases (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and RNA modifications and cancer (1 paper). Margaret J. McMillin is often cited by papers focused on Genomics and Rare Diseases (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and RNA modifications and cancer (1 paper). Margaret J. McMillin collaborates with scholars based in United States, Switzerland and Australia. Margaret J. McMillin's co-authors include Michael J. Bamshad, Kathryn M. Shively, Jay Shendure, Anita E. Beck, Heidi Gildersleeve, Karin M. Dent, Tracy Brazg, Joon‐Ho Yu, Holly K. Tabor and Michael Regnier and has published in prestigious journals such as The American Journal of Human Genetics, Mammalian Genome and American Journal of Medical Genetics Part A.

In The Last Decade

Margaret J. McMillin

6 papers receiving 281 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Margaret J. McMillin United States	6	160	130	73	49	37	6	286
Vanessa Rangel Miller United States	8	129 0.8×	113 0.9×	20 0.3×	27 0.6×	11 0.3×	10	249
Birsen Karaman Türkiye	12	157 1.0×	180 1.4×	24 0.3×	21 0.4×	24 0.6×	58	345
Amy Feldman Lewanda United States	10	271 1.7×	133 1.0×	39 0.5×	25 0.5×	10 0.3×	16	370
Stacey Hume Canada	10	68 0.4×	108 0.8×	17 0.2×	14 0.3×	15 0.4×	19	207
Anna R. Duncan United States	8	52 0.3×	182 1.4×	30 0.4×	21 0.4×	39 1.1×	9	287
Jan Maarten Cobben Netherlands	11	180 1.1×	145 1.1×	51 0.7×	32 0.7×	5 0.1×	18	331
Marta Alonso Spain	8	52 0.3×	94 0.7×	36 0.5×	108 2.2×	8 0.2×	35	335
Catherine Metaxotou Greece	12	188 1.2×	130 1.0×	36 0.5×	18 0.4×	15 0.4×	35	334
Chiara Castronovo Italy	9	183 1.1×	122 0.9×	22 0.3×	41 0.8×	5 0.1×	16	275
Joseph Cabral United States	4	67 0.4×	99 0.8×	10 0.1×	105 2.1×	9 0.2×	4	296

Countries citing papers authored by Margaret J. McMillin

Since Specialization

Citations

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

Fields of papers citing papers by Margaret J. McMillin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Margaret J. McMillin. 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 Margaret J. McMillin. The network helps show where Margaret J. McMillin may publish in the future.

Co-authorship network of co-authors of Margaret J. McMillin

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

All Works

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6 of 6 papers shown

1.

Morgan, Angela, Cristina Mei, Damien Lederer, et al.. (2015). Speech and language in a genotyped cohort of individuals with Kabuki syndrome. American Journal of Medical Genetics Part A. 167(7). 1483–1492. 27 indexed citations

2.

Beck, Anita E., et al.. (2014). Genotype‐phenotype relationships in Freeman–Sheldon syndrome. American Journal of Medical Genetics Part A. 164(11). 2808–2813. 36 indexed citations

3.

Buckingham, Kati J., Margaret J. McMillin, Margaret M. Brassil, et al.. (2013). Multiple mutant T alleles cause haploinsufficiency of Brachyury and short tails in Manx cats. Mammalian Genome. 24(9-10). 400–408. 37 indexed citations

4.

Beck, Anita E., Margaret J. McMillin, Heidi Gildersleeve, et al.. (2013). Spectrum of mutations that cause distal arthrogryposis types 1 and 2B. American Journal of Medical Genetics Part A. 161(3). 550–555. 53 indexed citations

5.

Below, Jennifer E., Dawn Earl, Kathryn M. Shively, et al.. (2012). Whole-Genome Analysis Reveals that Mutations in Inositol Polyphosphate Phosphatase-like 1 Cause Opsismodysplasia. The American Journal of Human Genetics. 92(1). 137–143. 44 indexed citations

6.

Tabor, Holly K., Tracy Brazg, Margaret J. McMillin, et al.. (2012). Informed consent for whole genome sequencing: A qualitative analysis of participant expectations and perceptions of risks, benefits, and harms. American Journal of Medical Genetics Part A. 158A(6). 1310–1319. 89 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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