Laura Davis Keppen

1.3k total citations
23 papers, 887 citations indexed

About

Laura Davis Keppen is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Laura Davis Keppen has authored 23 papers receiving a total of 887 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Molecular Biology and 5 papers in Genetics. Recurrent topics in Laura Davis Keppen's work include Metabolism and Genetic Disorders (4 papers), Hereditary Neurological Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Laura Davis Keppen is often cited by papers focused on Metabolism and Genetic Disorders (4 papers), Hereditary Neurological Disorders (4 papers) and Neurogenetic and Muscular Disorders Research (4 papers). Laura Davis Keppen collaborates with scholars based in United States, Netherlands and Belgium. Laura Davis Keppen's co-authors include Pedro Mancías, James R. Lupski, Ian J. Butler, Craig M. McDonald, Laura E. Warner, Virginia P. Johnson, Owen M. Rennert, Marilyn J. Bull, Theodore J. Pysher and Gerald Salen and has published in prestigious journals such as Nature Genetics, Neurology and The Journal of Pediatrics.

In The Last Decade

Laura Davis Keppen

23 papers receiving 863 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laura Davis Keppen United States 14 419 400 182 157 125 23 887
Sonia Ciarmatori Germany 11 312 0.7× 629 1.6× 190 1.0× 88 0.6× 31 0.2× 11 1.0k
Chikahiko Numakura Japan 22 435 1.0× 688 1.7× 184 1.0× 338 2.2× 144 1.2× 60 1.4k
Christine Verellen Belgium 11 650 1.6× 570 1.4× 271 1.5× 87 0.6× 35 0.3× 14 1.2k
J. Colomer Spain 17 214 0.5× 479 1.2× 86 0.5× 84 0.5× 137 1.1× 42 934
Kenji Nanao Japan 10 235 0.6× 220 0.6× 97 0.5× 80 0.5× 78 0.6× 17 561
Yorck Hellenbroich Germany 17 527 1.3× 661 1.7× 85 0.5× 277 1.8× 24 0.2× 44 952
Shen-Xing Murong China 13 170 0.4× 348 0.9× 38 0.2× 218 1.4× 90 0.7× 30 774
Stephan Niemann Germany 18 232 0.6× 668 1.7× 75 0.4× 184 1.2× 565 4.5× 26 1.6k
Ginat Narkis Israel 14 95 0.2× 528 1.3× 132 0.7× 127 0.8× 38 0.3× 23 836
Masao Mato Japan 16 147 0.4× 293 0.7× 360 2.0× 103 0.7× 87 0.7× 66 883

Countries citing papers authored by Laura Davis Keppen

Since Specialization
Citations

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

Fields of papers citing papers by Laura Davis Keppen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laura Davis Keppen. 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 Laura Davis Keppen. The network helps show where Laura Davis Keppen may publish in the future.

Co-authorship network of co-authors of Laura Davis Keppen

This figure shows the co-authorship network connecting the top 25 collaborators of Laura Davis Keppen. A scholar is included among the top collaborators of Laura Davis Keppen 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 Laura Davis Keppen. Laura Davis Keppen 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.
Flanagan, Jason, et al.. (2012). Bowen-Conradi: a common Hutterite condition that mimics trisomy 18.. PubMed. 65(6). 221–3, 225. 1 indexed citations
2.
Szigeti, Kinga, Wojciech Wiszniewski, Gulam Mustafa Saifi, et al.. (2007). Functional, histopathologic and natural history study of neuropathy associated with EGR2 mutations. Neurogenetics. 8(4). 257–262. 32 indexed citations
3.
Oglesbee, Devin, Miao He, Jerry Vockley, et al.. (2007). Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiency. Genetics in Medicine. 9(2). 108–116. 33 indexed citations
4.
Pedersen, Christina B., Claus Bischoff, Ernst Christensen, et al.. (2006). Variations in IBD (ACAD8) in Children with Elevated C4-Carnitine Detected by Tandem Mass Spectrometry Newborn Screening. Pediatric Research. 60(3). 315–320. 26 indexed citations
5.
Adam, Margaret P, Raoul C. M. Hennekam, Laura Davis Keppen, et al.. (2005). Marshall–Smith syndrome: Natural history and evidence of an osteochondrodysplasia with connective tissue abnormalities. American Journal of Medical Genetics Part A. 137A(2). 117–124. 29 indexed citations
6.
Warner, Laura E., Pedro Mancías, Ian J. Butler, et al.. (1998). Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies. Nature Genetics. 18(4). 382–384. 373 indexed citations
7.
Kulharya, Anita S., Jaime Garcia‐Heras, Heather B. Radtke, et al.. (1998). Prenatal diagnosis of a trisomy 17p derived from a de novo non‐mosaic satellited marker. Clinical Genetics. 54(5). 421–425. 14 indexed citations
8.
Irons, Mira, Ellen Roy Elias, Marilyn J. Bull, et al.. (1997). Treatment of Smith‐Lemli‐Opitz syndrome: Results of a multicenter trial. American Journal of Medical Genetics. 68(3). 311–314. 13 indexed citations
9.
Johnson, Virginia P., et al.. (1997). New syndrome of spondylospinal thoracic dysostosis with multiple pterygia and arthrogryposis. American Journal of Medical Genetics. 69(1). 73–78. 6 indexed citations
10.
Cambi, Franca, et al.. (1996). Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia. Neurology. 46(4). 1112–1117. 43 indexed citations
11.
Johnson, Virginia P., et al.. (1994). FISH detection of Wolf‐Hirschhorn syndorem: Exclusion of D4F26 as critical site. American Journal of Medical Genetics. 52(1). 70–74. 19 indexed citations
12.
Keppen, Laura Davis, et al.. (1992). Clinical phenotype and molecular analysis of a three‐generation family with an interstitial deletion of the short arm of chromosome 5. American Journal of Medical Genetics. 44(3). 356–360. 15 indexed citations
13.
Keppen, Laura Davis, Susanne M. Gollin, Joanna J. Seibert, & Jesse E. Sisken. (1991). Roberts syndrome with normal cell division. American Journal of Medical Genetics. 38(1). 21–24. 6 indexed citations
14.
Brodsky, Michael C., Laura Davis Keppen, Charles D. Rice, & Judith D. Ranells. (1990). Ocular and Systemic Findings in the Aarskog (Facial-digital-genital) Syndrome. American Journal of Ophthalmology. 109(4). 450–456. 7 indexed citations
15.
Keppen, Laura Davis, et al.. (1990). Hypogonadotropic hypogonadism in mentally retarded adults with microphthalmia and clinical anophthalmia. American Journal of Medical Genetics. 36(3). 285–287. 8 indexed citations
16.
Keppen, Laura Davis, Daniel J. Moore, & Donald J. Cannon. (1990). Zinc nutrition in fetal alcohol syndrome.. PubMed. 11(2). 375–80. 7 indexed citations
17.
Keppen, Laura Davis, James W. Fasules, A. Wesley Burks, et al.. (1988). Confirmation of autosomal dominant transmission of the DiGeorge malformation complex. The Journal of Pediatrics. 113(3). 506–508. 22 indexed citations
18.
Keppen, Laura Davis, Muhammad M. Husain, & Robert C. Woody. (1987). X‐linked myotubular myopathy: intrafamilial variability and normal muscle biopsy in a heterozygous female. Clinical Genetics. 32(2). 95–99. 15 indexed citations
19.
Keppen, Laura Davis, Mark Leppert, Peter O'Connell, et al.. (1987). Etiological heterogeneity in X-linked spastic paraplegia.. PubMed. 41(5). 933–43. 62 indexed citations
20.
Keppen, Laura Davis & Owen M. Rennert. (1983). Silver‐Russell syndrome with absence of digits and syndactylism of the fingers. Clinical Genetics. 24(6). 453–455. 4 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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