James R. Seip

428 total citations
12 papers, 274 citations indexed

About

James R. Seip is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, James R. Seip has authored 12 papers receiving a total of 274 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 6 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in James R. Seip's work include Genetic Syndromes and Imprinting (11 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). James R. Seip is often cited by papers focused on Genetic Syndromes and Imprinting (11 papers), Prenatal Screening and Diagnostics (6 papers) and Genomic variations and chromosomal abnormalities (5 papers). James R. Seip collaborates with scholars based in United States, Germany and Japan. James R. Seip's co-authors include Peter K. Rogan, Daniel J. Driscoll, Merlin G. Butler, Suzanne B. Cassidy, Barry G. Baylen, Deborah Belchis, Edward O. Bixler, Virginia P. Johnson, Shinji Saitoh and Robert D. Nicholls and has published in prestigious journals such as The American Journal of Human Genetics, The American Journal of Cardiology and Human Genetics.

In The Last Decade

James R. Seip

12 papers receiving 268 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
James R. Seip United States	7	225	171	111	29	24	12	274
A. Kleczkowska Belgium	11	282 1.3×	114 0.7×	109 1.0×	9 0.3×	23 1.0×	33	329
Carol English United Kingdom	9	139 0.6×	115 0.7×	64 0.6×	29 1.0×	42 1.8×	12	263
June-Anne Gold United States	7	268 1.2×	155 0.9×	68 0.6×	5 0.2×	36 1.5×	7	309
Natalie Blagowidow United States	6	157 0.7×	190 1.1×	22 0.2×	15 0.5×	19 0.8×	10	253
Xiaoyuan Zhong United States	4	139 0.6×	67 0.4×	15 0.1×	20 0.7×	9 0.4×	5	219
Erika Carter United States	10	268 1.2×	118 0.7×	82 0.7×	6 0.2×	26 1.1×	15	338
Sheona Watson-Scales United Kingdom	9	121 0.5×	101 0.6×	36 0.3×	14 0.5×	13 0.5×	10	305
Nicolás W. Martín Australia	7	77 0.3×	74 0.4×	15 0.1×	13 0.4×	23 1.0×	10	210
Hannaleena Kokkonen Finland	8	173 0.8×	152 0.9×	83 0.7×	4 0.1×	12 0.5×	20	238
Sohan Punia United States	7	135 0.6×	113 0.7×	9 0.1×	15 0.5×	34 1.4×	12	274

Countries citing papers authored by James R. Seip

Since Specialization

Citations

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

Fields of papers citing papers by James R. Seip

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James R. Seip. 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 James R. Seip. The network helps show where James R. Seip may publish in the future.

Co-authorship network of co-authors of James R. Seip

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

All Works

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12 of 12 papers shown

1.

Rogan, Peter K., James R. Seip, Lisa White, et al.. (1998). Relaxation of imprinting in Prader-Willi syndrome. Human Genetics. 103(6). 694–694. 13 indexed citations

2.

Butler, Merlin G., Lora K. Hedges, Peter K. Rogan, et al.. (1997). Klinefelter and trisomy X syndromes in patients with Prader-Willi syndrome and uniparental maternal disomy of chromosome 15—A coincidence?. American Journal of Medical Genetics. 72(1). 111–114. 17 indexed citations

3.

Butler, Merlin G., Lora K. Hedges, Peter K. Rogan, et al.. (1997). Klinefelter and trisomy X syndromes in patients with Prader‐Willi syndrome and uniparental maternal disomy of chromosome 15—A coincidence?. American Journal of Medical Genetics. 72(1). 111–114. 1 indexed citations

4.

Saitoh, Shinji, Karin Buiting, Suzanne B. Cassidy, et al.. (1997). Clinical spectrum and molecular diagnosis of Angelman and Prader‐Willi syndrome patients with an imprinting mutation. American Journal of Medical Genetics. 68(2). 195–206. 3 indexed citations

5.

Saitoh, Shinji, Karin Buiting, Suzanne B. Cassidy, et al.. (1997). Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation. American Journal of Medical Genetics. 68(2). 195–206. 76 indexed citations

6.

Vgontzas, Alexandros N., Anthony Kales, James R. Seip, et al.. (1996). Relationship of sleep abnormalities to patient genotypes in Prader-Willi syndrome. American Journal of Medical Genetics. 67(5). 478–482. 42 indexed citations

7.

Seip, James R., et al.. (1996). Association of a mosaic chromosomal 22q 11 deletion with hypoplastic left heart syndrome. The American Journal of Cardiology. 77(11). 1023–1025. 34 indexed citations

8.

Vgontzas, Alexandros N., Anthony Kales, James R. Seip, et al.. (1996). Relationship of sleep abnormalities to patient genotypes in Prader‐Willi syndrome. American Journal of Medical Genetics. 67(5). 478–482. 1 indexed citations

9.

Rogan, Peter K., James R. Seip, Daniel J. Driscoll, et al.. (1996). Distinct 15q genotypes in Russell‐Silver and ring 15 syndromes. American Journal of Medical Genetics. 62(1). 10–15. 3 indexed citations

10.

Rogan, Peter K., James R. Seip, Daniel J. Driscoll, et al.. (1996). Distinct 15q genotypes in Russell‐Silver and ring 15 syndromes. American Journal of Medical Genetics. 62(1). 10–15. 36 indexed citations

11.

Saitoh, Shinji, Robert D. Nicholls, & James R. Seip. (1994). The imprinted SNRPN gene is associated with a polycistronic mRNA and an imprinting control element. The American Journal of Human Genetics. 55. 29. 1 indexed citations

12.

Woodage, Trevor, Madhuri Prasad, Joanne Dixon, et al.. (1994). Bloom syndrome and maternal uniparental disomy for chromosome 15.. PubMed. 55(1). 74–80. 47 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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