Rebecca C. Tyler - Concepedia

Author

Rebecca C. Tyler

Medical College of Wisconsin

Also Known As

R Tyler, R. C. Tyler, R.C. Tyler, Rebecca C Tyler, Rebecca C. Tyler, Rebecca Tyler

Publications

827

Citations

H-Index

Concepts

All Affiliations

Medical College of Wisconsin Children's Hospital of Wisconsin University of Mississippi Medical Center Einstein Medical Center Philadelphia University of Calgary

About

Rebecca C. Tyler is an author at Medical College of Wisconsin specializing in genetics, medicine, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	336
2	Molecular Genetics	3	3	190
3	Public Health	1	1	48
4	Biology	1	1	84
5	Molecular Medicine	1	1	58

Rebecca C. Tyler

Publications

781

Citations

H-Index

Page 1

	Year	Citations
PITX2 and FOXC1 spectrum of mutations in ocular syndromes Linda M. Reis, Rebecca C. Tyler, Bethany A. Kloss, European Journal of Human Genetics Ocular DiseaseOphthalmologyGenetic DisorderGeneticsOcular Pathology	2012	146
BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome Linda M. Reis, Rebecca C. Tyler, Kala F. Schilter, Human Genetics	2011	118
Novel <i>SOX2</i> mutations and genotype–phenotype correlation in anophthalmia and microphthalmia Adele Schneider, Tanya Bardakjian, Linda M. Reis, American Journal of Medical Genetics Part A	2009	112
Whole exome sequencing in dominant cataract identifies a new causative factor, CRYBA2, and a variety of novel alleles in known genes Linda M. Reis, Rebecca C. Tyler, Sanaa Muheisen, Human Genetics BiologyDominant CataractAllelic VariantNew Causative FactorGenetics	2013	84
Mutation analysis of <i>B3GALTL</i> in Peters Plus syndrome Linda M. Reis, Rebecca C. Tyler, Omar Abdul‐Rahman, American Journal of Medical Genetics Part A	2008	60
PITX2 deficiency and associated human disease: insights from the zebrafish model Kathryn Hendee, Sanaa Muheisen, Linda M. Reis, Human Molecular Genetics GeneticsExperimental PathologyPathologyMolecular GeneticsDisease Gene Identification	2018	58
<i>FOXE3</i> plays a significant role in autosomal recessive microphthalmia Linda M. Reis, Rebecca C. Tyler, Adele Schneider, American Journal of Medical Genetics Part A	2010	54
Novel <i><scp>B3GALTL</scp></i> mutations in classic Peters plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes Eric Weh, Linda M. Reis, Rebecca C. Tyler, Clinical Genetics GeneticsGenetic EpidemiologyPathologyMolecular GeneticsDisease Gene Identification	2013	48
VSX2 mutations in autosomal recessive microphthalmia. Linda M. Reis, Ayesha Khan, Ariana Kariminejad, PubMed	2011	30
Examination of SOX2 in variable ocular conditions identifies a recurrent deletion in microphthalmia and lack of mutations in other phenotypes. Linda M. Reis, Rebecca C. Tyler, Adele Schneider, PubMed	2010	19

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