Andrew C. Lidral - Concepedia

Author

Andrew C. Lidral

Also Known As

A C Lidral, A. C. Lidral, A.C. Lidral, Andrew C Lidral, Andrew C. Lidral, Andrew Carl Lidral, Andrew Lidral, Andrew C. Lidral, Pober, Barbara R.

Publications

7.3K

Citations

H-Index

Concepts

All Affiliations

University of Iowa University of Pittsburgh Universidad de Antioquia University of Southern Denmark Johns Hopkins University

About

Andrew C. Lidral is an author at University of Iowa specializing in medicine, genetics, and developmental biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	19	3.4K
2	Public Health	4	4	143
3	Biostatistics	2	2	88
4	Anatomy	1	1	78
5	Biology	1	1	56

Andrew C. Lidral

Publications

6.4K

Citations

H-Index

Page 1

	Year	Citations
Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes Shinji Kondo, Brian C. Schutte, Rebecca J. Richardson, Nature Genetics Developmental AnomalyPopliteal Pterygium SyndromesMendelian DisorderGenetic DisorderGenetics	2002	891
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4 Terri H. Beaty, Jeffrey C. Murray, Mary L. Marazita, Nature Genetics Genome-wide Association StudyAllelic VariantDevelopmental BiologyGeneticsCleft Palate Identifies	2010	583
Interferon Regulatory Factor 6 ( <i>IRF6</i> ) Gene Variants and the Risk of Isolated Cleft Lip or Palate Theresa M. Zucchero, Margaret E. Cooper, Brion S. Maher, New England Journal of Medicine	2004	581
Association of MSX1 and TGFB3 with Nonsyndromic Clefting in Humans Andrew C. Lidral, Paul A. Romitti, Ann M. Basart, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyPathologyCraniofacial AnomaliesNonsyndromic Clefting	1998	302
Candidate genes for nonsyndromic cleft lip and palate and maternal cigarette smoking and alcohol consumption: Evaluation of genotype-environment interactions from a population-based case-control study of orofacial clefts Paul A. Romitti, Andrew C. Lidral, Ronald G. Munger, Teratology	1999	241
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 Role of MSX1 in Human Tooth Agenesis Andrew C. Lidral, B.C. Reising Journal of Dental Research Developmental AnomalyOdontologyDental MorphologyDevelopmental BiologyCraniofacial Disorder	2002	210
Autosomal Dominant Craniometaphyseal Dysplasia Is Caused by Mutations in the Transmembrane Protein ANK Ernst Reichenberger, Valdenize Tiziani, Shôji Watanabe, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderTransmembrane Protein AnkGenetic Disorder	2001	195
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

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