Eric A. Wulfsberg

1.7k total citations
47 papers, 1.2k citations indexed

About

Eric A. Wulfsberg is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Eric A. Wulfsberg has authored 47 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 19 papers in Molecular Biology and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Eric A. Wulfsberg's work include Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (9 papers) and Cleft Lip and Palate Research (8 papers). Eric A. Wulfsberg is often cited by papers focused on Genomic variations and chromosomal abnormalities (13 papers), Prenatal Screening and Diagnostics (9 papers) and Cleft Lip and Palate Research (8 papers). Eric A. Wulfsberg collaborates with scholars based in United States, Mexico and Italy. Eric A. Wulfsberg's co-authors include Julie Leana‐Cox, Iosif W. Lurie, Iain McIntosh, Diane E. Hoffmann, Chen Sun, Ivana Klisak, Andrew B. Campbell, Terri H. Beaty, Amy Feldman Lewanda and Joseph Lopreiato and has published in prestigious journals such as JAMA, Genomics and Journal of Medical Genetics.

In The Last Decade

Eric A. Wulfsberg

45 papers receiving 1.1k citations

Peers

Countries citing papers authored by Eric A. Wulfsberg

Since Specialization

Citations

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

Fields of papers citing papers by Eric A. Wulfsberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric A. Wulfsberg. 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 Eric A. Wulfsberg. The network helps show where Eric A. Wulfsberg may publish in the future.

Co-authorship network of co-authors of Eric A. Wulfsberg

This figure shows the co-authorship network connecting the top 25 collaborators of Eric A. Wulfsberg. A scholar is included among the top collaborators of Eric A. Wulfsberg 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 Eric A. Wulfsberg. Eric A. Wulfsberg 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

#	Work	Indexed citations
1	Familial testicular germ cell tumor: no associated syndromic pattern identified 2014 ·Hereditary Cancer in Clinical Practice ·Christine M. Mueller, Larissa A. Korde, Mary L. McMaster, June A. Peters, Gennady Bratslavsky, (unknown), Alexander Ling, Christian P. Kratz, Eric A. Wulfsberg, Philip S. Rosenberg, Mark H. Greene	2
2	A Case-Control Study of Nonsyndromic Oral Clefts in Maryland 2001 ·Annals of Epidemiology ·Terri H. Beaty, (unknown), Jacqueline B. Hetmanski, Yu Fan, Joanna S. Zeiger, K.-Y. Liang, (unknown), Craig A. VanderKolk, (unknown), Eric A. Wulfsberg, Gerald V. Raymond, Susan R. Panny, Iain McIntosh	97
3	Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome 2000 ·Mammalian Genome ·Russell A. Norris, (unknown), Clara S. Moore, Gail Stetten, (unknown), Ethylin Wang Jabs, Eric A. Wulfsberg, Jack C. Yu, Michael J. Kern	40
4	Third Prader-Willi syndrome phenotype due to maternal uniparental disomy 15 with mosaic trisomy 15 2000 ·American Journal of Medical Genetics ·(unknown), Judith Stamberg, (unknown), Eric A. Wulfsberg	22
5	No Evidence of Linkage for Cleft Lip with or without Cleft Palate to a Marker Near the Transforming Growth Factor Alpha Locus in Two Populations 1997 ·Human Heredity ·Diego F. Wyszynski, Nancy E. Maestri, Amy Feldman Lewanda, Iain McIntosh, Anne Smith, (unknown), (unknown), Eric A. Wulfsberg, Terri H. Beaty	23
6	Familial DiGeorge/velocardiofacial syndrome with deletions of chromosome area22q11.2: Report of five families with a review of the literature 1996 ·American Journal of Medical Genetics ·Julie Leana‐Cox, (unknown), (unknown), (unknown), Eric A. Wulfsberg	62
7	Confirmation of the catania brachydactylous type of acrofacial dysostosis: Report of a second family 1996 ·American Journal of Medical Genetics ·Eric A. Wulfsberg, Andrew B. Campbell, Iosif W. Lurie, (unknown)	5
8	What's in a name? chromosome 22q abnormalities and the DiGeorge, velocardiofacial, and conotruncal anomalies face syndromes 1996 ·American Journal of Medical Genetics ·Eric A. Wulfsberg, Julie Leana‐Cox, Giovanni Neri	38
9	Evidence for an association between markers on chromosome 19q and non-syndromic cleft lip with or without cleft palate in two groups of multiplex families 1996 ·Human Genetics ·Diego F. Wyszynski, Nancy E. Maestri, Iain McIntosh, Elizabeth A. Smith, Amy Feldman Lewanda, (unknown), (unknown), Eric A. Wulfsberg, Terri H. Beaty	49
10	Alpha 1-antitrypsin deficiency. Impact of genetic discovery on medicine and society 1994 ·JAMA ·Eric A. Wulfsberg	16
11	Phenotypic variability of del(2) (q22-q23): report of a case with a review of the literature. 1994 ·PubMed ·Iosif W. Lurie, (unknown), Lynne S. Rosenblum‐Vos, Eric A. Wulfsberg	34
12	Gorlin syndrome (naevoid basal cell carcinoma syndrome): Prenatal detection in a fetus with macrocephaly and ventriculomegaly 1994 ·Prenatal Diagnosis ·W. Allen Hogge, (unknown), (unknown), (unknown), Eric A. Wulfsberg, Leslie J. Raffel	9
13	“Holoprosencephaly‐polydactyly” (pseudotrisomy 13) syndrome: Expansion of the phenotypic spectrum 1993 ·American Journal of Medical Genetics ·Iosif W. Lurie, Eric A. Wulfsberg	18
14	Characterization of de novo duplications in eight patients by using fluorescence in situ hybridization with chromosome-specific DNA libraries. 1993 ·Europe PMC (PubMed Central) ·Julie Leana‐Cox, Sondra W. Levin, (unknown), Eric A. Wulfsberg, (unknown), Leslie J. Raffel, Beth A. Sullivan, Stuart Schwartz	25
15	Autosomal dominant tetramelic postaxial oligodactyly 1993 ·American Journal of Medical Genetics ·Eric A. Wulfsberg, (unknown), (unknown)	7
16	Vertebral hypersegmentation in a case of the VATER association 1992 ·American Journal of Medical Genetics ·Eric A. Wulfsberg, (unknown), Ronald Thomas	5
17	Chondrodysplasia punctata: A boy with X‐linked recessive chondrodysplasia punctata due to an inherited X‐Y translocation with a current classification of these disorders 1992 ·American Journal of Medical Genetics ·Eric A. Wulfsberg, Jerri Curtis, (unknown)	33
18	The inheritance of conotruncal malformations: a review and report of two siblings with tetralogy of Fallot with pulmonary atresia 1991 ·Clinical Genetics ·Eric A. Wulfsberg, (unknown), John W. Moore	12
19	Monozygotic twin girls with diploid/triploid chromosome mosaicism and cutaneous pigmentary dysplasia 1991 ·Clinical Genetics ·Eric A. Wulfsberg, (unknown), (unknown)	25
20	Chromosome 10qter deletion syndrome: A review and report of three new cases 1989 ·American Journal of Medical Genetics ·Eric A. Wulfsberg, (unknown), Christopher Cunniff, Marilyn C. Jones, (unknown)	56

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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