• 1606 Citations
  • 23 h-Index
19992019
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Fingerprint Dive into the research topics where Claire L. Simpson is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 7 Similar Profiles
Refractive Errors Medicine & Life Sciences
Myopia Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Genome Medicine & Life Sciences
Meta-Analysis Medicine & Life Sciences
Genes Medicine & Life Sciences
Genome-Wide Association Study Medicine & Life Sciences
Exome Medicine & Life Sciences

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Research Output 1999 2019

  • 1606 Citations
  • 23 h-Index
  • 45 Article
  • 3 Review article
  • 2 Comment/debate
  • 2 Letter

Exome genotyping and linkage analysis identifies two novel linked regions and replicates two others for myopia in Ashkenazi Jewish families

Simpson, C., Musolf, A. M., Li, Q., Portas, L., Murgia, F., Cordero, R. Y., Cordero, J. B., Moiz, B. A., Holzinger, E. R., Middlebrooks, C. D., Lewis, D. D., Bailey-Wilson, J. E. & Stambolian, D., Jan 31 2019, In : BMC Medical Genetics. 20, 1, 27.

Research output: Contribution to journalArticle

Exome
Myopia
Refractive Errors
Haplotypes
Genome

Genome-wide scans of myopia in Pennsylvania Amish families reveal significant linkage to 12q15, 8q21.3 and 5p15.33

Musolf, A. M., Simpson, C., Alexander, T. A., Portas, L., Murgia, F., Ciner, E. B., Stambolian, D. & Bailey-Wilson, J. E., Apr 1 2019, In : Human genetics. 138, 4, p. 339-354 16 p.

Research output: Contribution to journalArticle

Amish
Myopia
Genome
Color Vision Defects
Inborn Genetic Diseases

Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing

Musolf, A. M., Ho, W. S. C., Long, K. A., Zhuang, Z., Argersinger, D. P., Sun, H., Moiz, B. A., Simpson, C., Mendelevich, E. G., Bogdanov, E. I., Bailey-Wilson, J. E. & Heiss, J. D., Oct 1 2019, In : European Journal of Human Genetics. 27, 10, p. 1599-1610 12 p.

Research output: Contribution to journalArticle

Exome
Haplotypes
Cerebellum
Genes
Brain Stem
5 Citations (Scopus)

Fetal—Not Maternal—APOL1 Genotype Associated with Risk for Preeclampsia in Those with African Ancestry

Reidy, K. J., Hjorten, R. C., Simpson, C., Rosenberg, A. Z., Rosenblum, S. D., Kovesdy, C., Tylavsky, F., Myrie, J., Ruiz, B. L., Haque, S., Mozhui, K., Nelson, G. W., David, V. A., Yang, X., Suzuki, M., Jacob, J., Reznik, S. E., Kaskel, F. J., Kopp, J. B., Winkler, C. A. & 1 others, Davis, R., Sep 6 2018, In : American Journal of Human Genetics. 103, 3, p. 367-376 10 p.

Research output: Contribution to journalArticle

Apolipoproteins
Pre-Eclampsia
Genotype
Mothers
Pregnancy
30 Citations (Scopus)

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

CREAM, 23andMe Research Team & UK Biobank Eye and Vision Consortium, Jun 1 2018, In : Nature Genetics. 50, 6, p. 834-848 15 p.

Research output: Contribution to journalArticle

Refractive Errors
Genome-Wide Association Study
Meta-Analysis
Light
Retina