Allen N. Lamb

5.4k total citations
50 papers, 2.2k citations indexed

About

Allen N. Lamb is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Allen N. Lamb has authored 50 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 22 papers in Molecular Biology and 15 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Allen N. Lamb's work include Genomic variations and chromosomal abnormalities (35 papers), Prenatal Screening and Diagnostics (15 papers) and Chromosomal and Genetic Variations (15 papers). Allen N. Lamb is often cited by papers focused on Genomic variations and chromosomal abnormalities (35 papers), Prenatal Screening and Diagnostics (15 papers) and Chromosomal and Genetic Variations (15 papers). Allen N. Lamb collaborates with scholars based in United States, United Kingdom and Canada. Allen N. Lamb's co-authors include J. Malcolm Shick, Lisa G. Shaffer, Sarah T. South, James Bartley, Bing Huang, Yi Ning, Hutton M. Kearney, Bassem A. Bejjani, Shengbiao Wang and Charles Lee and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Genome Research and American Journal of Obstetrics and Gynecology.

In The Last Decade

Allen N. Lamb

49 papers receiving 2.0k citations

Peers

Allen N. Lamb

GENET

PPCH

Michael J. Friez United States

F.F.B. Elder United States

Indrajit Nanda Germany

Wilbur R. Harrison United States

Ozren Bogdanović Australia

Patrick Western Australia

John Longshore United States

Claudia Kappen United States

Hans Grüneberg United Kingdom

Hiroyuki Sasaki Japan

Michael J. Friez United States

Allen N. Lamb

1.6k ×1.0

GENET

1.7k ×1.8

135 ×0.2

PPCH

161 ×0.6

180 ×0.9

Citations per year, relative to Allen N. Lamb Allen N. Lamb (= 1×) peers Michael J. Friez

Countries citing papers authored by Allen N. Lamb

Since Specialization

Citations

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

Fields of papers citing papers by Allen N. Lamb

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Allen N. Lamb. 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 Allen N. Lamb. The network helps show where Allen N. Lamb may publish in the future.

Co-authorship network of co-authors of Allen N. Lamb

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

All Works

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20 of 20 papers shown

Saros, Jasmine E., Robert M. Northington, Allen N. Lamb, et al.. (2025). Abrupt transformation of West Greenland lakes following compound climate extremes associated with atmospheric rivers. Proceedings of the National Academy of Sciences. 122(4). e2413855122–e2413855122. 5 indexed citations

Wen, Ting, Janice C. Palumbos, Betsy Ostrander, et al.. (2025). Vertical inheritance and unique differential phenotypes of reciprocal recombinant chromosome 18 within a multi-generation family. European Journal of Human Genetics. 34(1). 128–133.

Gotway, Garrett, et al.. (2019). A Novel Homozygous Deletion within the <b><i>FRY</i></b> Gene Associated with Nonsyndromic Developmental Delay. Cytogenetic and Genome Research. 159(1). 19–25. 3 indexed citations

Waggoner, Darrel, Karen E. Wain, Adrian M. Dubuc, et al.. (2018). Yield of additional genetic testing after chromosomal microarray for diagnosis of neurodevelopmental disability and congenital anomalies: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 20(10). 1105–1113. 46 indexed citations

LaGrave, Danielle, et al.. (2016). Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder. European Journal of Medical Genetics. 59(9). 470–473. 19 indexed citations

South, Sarah T., Charles Lee, Allen N. Lamb, Anne W. Higgins, & Hutton M. Kearney. (2013). ACMG Standards and Guidelines for constitutional cytogenomic microarray analysis, including postnatal and prenatal applications: revision 2013. Genetics in Medicine. 15(11). 901–909. 232 indexed citations

Barber, John, Jill A. Rosenfeld, Nicola Foulds, et al.. (2013). 8p23.1 duplication syndrome; common, confirmed, and novel features in six further patients. American Journal of Medical Genetics Part A. 161(3). 487–500. 33 indexed citations

Sahoo, Trilochan, Aaron Theisen, Jill A. Rosenfeld, et al.. (2011). Copy number variants of schizophrenia susceptibility loci are associated with a spectrum of speech and developmental delays and behavior problems. Genetics in Medicine. 13(10). 868–880. 75 indexed citations

Sahoo, Trilochan, Aaron Theisen, Pedro A. Sanchez‐Lara, et al.. (2011). Microdeletion 20p12.3 involving BMP2 contributes to syndromic forms of cleft palate. American Journal of Medical Genetics Part A. 155(7). 1646–1653. 53 indexed citations

10.

Neill, Nicholas J., Blake C. Ballif, Allen N. Lamb, et al.. (2011). Recurrence, submicroscopic complexity, and potential clinical relevance of copy gains detected by array CGH that are shown to be unbalanced insertions by FISH. Genome Research. 21(4). 535–544. 41 indexed citations

11.

Kearney, Hutton M., Sarah T. South, Daynna J. Wolff, et al.. (2011). American College of Medical Genetics recommendations for the design and performance expectations for clinical genomic copy number microarrays intended for use in the postnatal setting for detection of constitutional abnormalities. Genetics in Medicine. 13(7). 676–679. 73 indexed citations

12.

Lamb, Allen N.. (2011). Laboratory Aspects of Prenatal Microarray Analysis. Clinics in Laboratory Medicine. 31(4). 615–630. 2 indexed citations

13.

Duker, Angela L., Blake C. Ballif, Erawati V. Bawle, et al.. (2010). Paternally inherited microdeletion at 15q11.2 confirms a significant role for the SNORD116 C/D box snoRNA cluster in Prader–Willi syndrome. European Journal of Human Genetics. 18(11). 1196–1201. 236 indexed citations

14.

Coppinger, Justine, Sarah Alliman, Allen N. Lamb, et al.. (2009). Whole‐genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray. Prenatal Diagnosis. 29(12). 1156–1166. 97 indexed citations

15.

Donnenfeld, Alan E. & Allen N. Lamb. (2003). Cytogenetics and molecular cytogenetics in prenatal diagnosis. Clinics in Laboratory Medicine. 23(2). 457–480. 2 indexed citations

16.

Donnenfeld, Alan E., et al.. (2002). Prenatal diagnosis from fetal urine in bladder outlet obstruction: Success rates for traditional cytogenetic evaluation and interphase fluorescence in situ hybridization. Genetics in Medicine. 4(6). 444–447. 8 indexed citations

17.

Lamb, Allen N. & Laurel L. Estabrooks. (2000). Prenatal interphase fluorescence in situ hybridization (FISH). Contemporary ob/gyn. 1 indexed citations

18.

Estop, A., et al.. (1998). Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis. Human Reproduction. 13(1). 124–127. 109 indexed citations

19.

Lanphear, Nancy, Allen N. Lamb, Sonya Oppenheimer, & Shirley Soukup. (1995). Supernumerary chromosome marker (1) in a developmentally delayed child. American Journal of Medical Genetics. 57(3). 400–402. 15 indexed citations

20.

Lloyd, Joyce A., Allen N. Lamb, & S. Steven Potter. (1987). Phylogenetic screening of the human genome: identification of differentially hybridizing repetitive sequence families.. Molecular Biology and Evolution. 4(2). 85–98. 8 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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