Katherine Neiswanger

Author

University of Pittsburgh ORCID

Also Known As

K Neiswanger, K. Neiswanger, K., Neiswanger, Katherine Neiswanger, Neiswanger, K

Publications

3.6K

Citations

H-Index

Concepts

All Affiliations

University of Pittsburgh West Virginia University University of Iowa University of Michigan The University of Texas Health Science Center at Houston

About

Katherine Neiswanger is an author at University of Pittsburgh specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	15	1K
2	Natural Sciences	4	4	397
3	Public Health	4	4	72
4	Engineering	1	1	265
5	Allergy	1	1	38

Katherine Neiswanger

Publications

Citations

H-Index

Page 1

	Year	Citations
Digital Three-Dimensional Photogrammetry: Evaluation of Anthropometric Precision and Accuracy Using a Genex 3D Camera System Seth M. Weinberg, Nicole Scott, Katherine Neiswanger, The Cleft Palate-Craniofacial Journal Engineering3D Pose EstimationAnatomy3D Body ScanningKinesiology	2004	265
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 Elizabeth J. Leslie, Jenna C. Carlson, John R. Shaffer, Human Molecular Genetics	2016	224
Mutations in BMP4 Are Associated with Subepithelial, Microform, and Overt Cleft Lip Satoshi Suzuki, Mary L. Marazita, Margaret E. Cooper, The American Journal of Human Genetics Overt Cleft LipDevelopmental BiologyGenetic DisorderGeneticsCraniofacial Development	2009	212
The human X-linked steroid sulfatase gene and a Y-encoded pseudogene: Evidence for an inversion of the Y chromosome during primate evolution Pauline H. Yen, Birgit Marsh, Elizabeth Allen, Cell Developmental BiologyGenetic DisorderGeneticsGenetic MechanismChromosome Biology	1988	178
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 Elizabeth J. Leslie, Huan Liu, Jenna C. Carlson, The American Journal of Human Genetics Genome-wide Association StudyDevelopmental BiologyEtiologic Missense VariantGenetic DisorderMedicine	2016	174
Intraobserver error associated with measurements of the hand Seth M. Weinberg, Nicole Scott, Katherine Neiswanger, American Journal of Human Biology	2005	136
The search for heterogeneity in insulin-dependent diabetes mellitus (IDDM): linkage studies, two-locus models, and genetic heterogeneity. Susan E. Hodge, Carol E. Anderson, Katherine Neiswanger, PubMed	1983	123
Association and linkage studies of the TAQI A1 allele at the dopamine D<sub>2</sub> receptor gene in samples of female and male alcoholics Katherine Neiswanger, Shirley Y. Hill, Barry B. Kaplan American Journal of Medical Genetics	1995	108
Face shape of unaffected parents with cleft affected offspring: combining three‐dimensional surface imaging and geometric morphometrics SD Naidoo, KM Bardi, CA Brandon, Orthodontics and Craniofacial Research	2009	102
Origins and antiquity of X-linked triallelic color vision systems in New World monkeys Stéphane Boissinot, Ying Tan, Song‐Kun Shyue, Proceedings of the National Academy of Sciences	1998	98

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