Alan Shanske

3.2k citations

84 papers · 1.9k indexed · h-index 26

Impact in

Genetics top 2%
- Genomic variations and chromosomal abnormalities
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Connective tissue disorders research
Sensory Systems top 5%
- Hearing, Cochlea, Tinnitus, Genetics

Papers in

Developmental Biology 4
Genetics 50
- Genomic variations and chromosomal abnormalities 17
- Connective tissue disorders research 11
- Cleft Lip and Palate Research 11
- Craniofacial Disorders and Treatments 10
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8

Co-authors: Bernice E. Morrow Robert W. Marion Sara Shanske Lisa Edelmann Venkat Pulijaal Elizabeth Spiteri Irwin M. Arias Michael Mosher
Journals: The American Journal of Human Genetics (7 papers)International Journal of Pediatric Otorhinolaryngology (4 papers)Pediatric Research (4 papers)Human Molecular Genetics (2 papers)Prenatal Diagnosis (2 papers)
Partner nations: United States United Kingdom Canada

In The Last Decade

Alan Shanske

80 papers receiving 1.8k citations

Peers

Countries citing papers authored by Alan Shanske

Since Specialization

Citations

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

Fields of papers citing papers by Alan Shanske

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alan Shanske. 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 Alan Shanske. The network helps show where Alan Shanske may publish in the future.

Co-authors

The 25 scholars most cited alongside Alan Shanske, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Alan Shanske Line = papers co-authored together Alan Shanske links everyone, so they are left out of the graph.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Germline mosacism in Shprintzen–Goldberg syndrome American Journal of Medical Genetics Part A ·Alan Shanske, James T. Goodrich, Leena Ala‐Kokko, Stuart G. Baker, Barbara Frederick, Brynn Levy	2012	5
2	Bilateral oblique facial clefts and extremity anomaly in an infant after intrauterine efavirenz exposure and review of its teratogenic risk AIDS ·Alan Shanske	2012	9
3	Genomic strategy identifies a missense mutation in WD‐repeat domain 65 (WDR65) in an individual with Van der Woude syndrome American Journal of Medical Genetics Part A ·Jelka Kernev-Štrajn, Akira Kinoshita, Jason L. Weirather, Myriam Peyrard‐Janvid, Renata Lúcia Leite Ferreira de Lima, Martine Dunnwald, Alan Shanske, Danilo Moretti‐Ferreira, Hannele Koillinen, Juha Kere, M. Adela Mansilla, Jeffrey C. Murray, Nishitani Sachiko, Brian C. Schutte	2011	10
4	Exome Sequence Identifies RIPK4 as the Bartsocas- Papas Syndrome Locus The American Journal of Human Genetics ·Karen S. Mitchell, James O’Sullivan, Caterina Missero, Ed Blair, Rose Richardson, Beverley Anderson, Dario Antonini, Jeffrey C. Murray, Alan Shanske, Brian C. Schutte, Rose-Anne Romano, Satrajit Sinha, Sanjeev S. Bhaskar, Graeme C. Black, Jill Dixon, Michael J. Dixon	2011	73
5	Buschke-Ollendorff Syndrome Archives of Dermatology ·Marta Widuch, Michael P. Whyte, Steven Mumm, Robert Phelps, Alan Shanske, William G. Totty, Steven R. Cohen	2010	17
6	Cervical vascular and upper airway asymmetry in velo-cardio-facial syndrome: Correlation of nasopharyngoscopy with MRA International Journal of Pediatric Otorhinolaryngology ·Indah Riski, Aneta Šedivková, Keivan Shifteh, Th. Lund, Allan Brook, Alan Shanske, Robert J. Shprintzen	2010	26
7	Interparietal bone (Os Incae) in craniosynostosis American Journal of Medical Genetics Part A ·June K. Wu, James T. Goodrich, Leslie A. Wells, Todd A. Miller, John B. Mulliken, Alan Shanske	2010	13
8	Retinoid signaling in inner ear development: A “Goldilocks” phenomenon American Journal of Medical Genetics Part A ·Dorothy A. Frenz, Wei Liu, Aleš Cvekl, Qing Xie, Lesley Wassef, Loredana Quadro, Karen Niederreither, Mark Maconochie, Alan Shanske	2010	46
9	Accelerated Spirometric Decline in New York City Firefighters With α;1-Antitrypsin Deficiency CHEST Journal ·Gisela I. Banauch, Mark Brantly, Gabriel Izbicki, Charles B. Hall, Alan Shanske, Eunice Achieng Anyona, Clayziane Lino Araújo Arêa Leão, Vasilios Christodoulou, Michael D. Weiden, David J. Prezant	2010	35
10	Clinical and molecular characterization of a patient with Langer–Giedion syndrome and mosaic del(8)(q22.3q24.13) American Journal of Medical Genetics Part A ·Alan Shanske, Ankita Patel, Christopher N. Bond, Brynn Levy, Hermann‐Josef Lüdecke	2008	15
11	Chorea associated with antiphospholipid antibodies in a patient with Kabuki syndrome American Journal of Medical Genetics Part A ·陳堉薇, Eric Segal, Alan Shanske, Catherine Driscoll	2007	9
12	Detection of an interstitial deletion of 2q21‐22 by high resolution comparative genomic hybridization in a child with multiple congenital anomalies and an apparent balanced translocation American Journal of Medical Genetics Part A ·Alan Shanske, Lisa Edelmann, 马广生, Philippe Gosset, Brynn Levy	2004	21
13	A Recurring FBN1 Gene Mutation in Neonatal Marfan Syndrome Archives of Pediatrics and Adolescent Medicine ·V. K. Obukhov, Ivanka Toudjarska, Andrew D. Racine, Petros Tsipouras, Michael W. Kilpatrick, Alan Shanske	2002	34
14	Diprosopus: A unique case and review of the literature Teratology ·June K. Wu, David A. Staffenberg, John B. Mulliken, Alan Shanske	2002	33
15	The Other Human Genome Archives of Pediatrics and Adolescent Medicine ·Alan Shanske, Sara Shanske, S. DiMauro	2001	18
16	Subtle radiographic findings of achondroplasia in patients with Crouzon syndrome with acanthosis nigricans due to an Ala391Glu substitution in FGFR3 American Journal of Medical Genetics ·كریم محمد ابراهیم محمد عطیة عطیة, John M. Graham, Ralph S. Lachman, Ethylin Wang Jabs, Kazuki Okajima, Kelly A. Przylepa, Alan Shanske, Kelly Chen, Julie Neidich, William R. Wilcox	2000	35
17	Philadelphia-negative chronic myelogenous leukemia in a patient with a unique complex translocation: 46,XY,t(9;12;15)(q34;q12;q21) Leukemia Research ·Alan Shanske, Hans Grünwald, Perry Cook, Nora Heisterkamp, John Groffen	1998	1
18	The Marshall syndrome: Report of a new family and review of the literature American Journal of Medical Genetics ·Alan Shanske, Timothy Charles Marshall, Robert J. Shprintzen, Robert W. Marion	1997	21
19	Craniofacial, limb, and abdominal anomalies in a distinct syndrome: Relation to the spectrum of Pfeiffer syndrome type 3 American Journal of Medical Genetics ·Constance M. Barone, Robert Marion, Alan Shanske, Ravelo V. Argamaso, 徐谦	1993	13
20	Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies Prenatal Diagnosis ·Lillian Y. F. Hsu, Sara Kaffe, Edmund C. Jenkins, Jascha Marnette, Peter Benn, Karen David, Kurt Hirschhorn, Ernest Lieber, Alan Shanske, Lawrence R. Shapiro, P.J.W. Rowell, Dorothy Warburton	1992	105

About Alan Shanske

Alan Shanske is a scholar working on Developmental Biology, Genetics, Sensory Systems, Genetics and Pediatrics, Perinatology and Child Health, having authored 84 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (17 papers), Connective tissue disorders research (11 papers), Cleft Lip and Palate Research (11 papers), Prenatal Screening and Diagnostics (10 papers), Craniofacial Disorders and Treatments (10 papers), Congenital heart defects research (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers) and Hedgehog Signaling Pathway Studies (8 papers). The work is most often cited by research in Genetics (931 citations), Sensory Systems (133 citations), Developmental Biology (41 citations), Pediatrics, Perinatology and Child Health (310 citations) and Molecular Biology (976 citations). Alan Shanske has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Bernice E. Morrow, Robert W. Marion, Sara Shanske, Lisa Edelmann, Venkat Pulijaal, Elizabeth Spiteri, Irwin M. Arias, Michael Mosher, Seymour Alpert and Rosalie Goldberg. Their work appears in journals such as The American Journal of Human Genetics, International Journal of Pediatric Otorhinolaryngology, Pediatric Research, Human Molecular Genetics and Prenatal Diagnosis.

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.

Explore authors with similar magnitude of impact