Chandrasekharappa, Settara C.

Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

Polymeropoulos, M. H., Lavedan, C., Leroy, E., Ide, S. E., Dehejia, A., Dutra, A., Pike, B., Root, H., Rubenstein, J., Boyer, R., et al. (1997) · Science

Parkinson's Disease Mechanisms and TreatmentsNuclear Receptors and Signaling

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A Hereditary Form of Small Intestinal Carcinoid Associated With a Germline Mutation in Inositol Polyphosphate Multikinase

Sei, Y., Zhao, X., Forbes, J., Szymczak, S., Li, Q., Trivedi, A., Voellinger, M., Joy, G., Feng, J., Whatley, M., et al. (2015) · Gastroenterology

Neuroendocrine Tumor Research AdvancesGenetic factors in colorectal cancer

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Review of disrupted sleep patterns in Smith–Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11.2 deletion

Boudreau, E. A., Johnson, K. P., Jackman, A. R., Blancato, J., Huizing, M., Bendavid, C., Jones, M., Chandrasekharappa, S. C., Lewy, A. J., Smith, A. C. M., et al. (2009) · American Journal of Medical Genetics Part A

Circadian rhythm and melatoninSleep and Wakefulness Research

Cited by 92

Pooling/bootstrap-based GWAS (pbGWAS) identifies new loci modifying the age of onset in PSEN1 p.Glu280Ala Alzheimer's disease

Vélez, J. I., Chandrasekharappa, S. C., Henao, E., Martinez, A. F., Harper, U., Jones, M., Solomon, B. D., Lopez, L., Garcia, G., Aguirre-Acevedo, D. C., et al. (2013) · Molecular Psychiatry

Alzheimer's disease research and treatmentsDementia and Cognitive Impairment Research

Cited by 44

Whole-Exome Sequencing for Diagnosis of Turner Syndrome: Toward Next-Generation Sequencing and Newborn Screening

Murdock, D. R., Donovan, F. X., Chandrasekharappa, S. C., Banks, N., Bondy, C., Muenke, M., & Kruszka, P. (2017) · The Journal of Clinical Endocrinology & Metabolism

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesGenomics and Rare Diseases

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