Curry, Cynthia J.
University of California, San Francisco
6 papers on CoChatORCID 0000-0001-7585-1940
Most cited papers
- Verified
Retinoic acid embryopathy
Lammer, E. J., Chen, D. T., Hoar, R. M., Agnish, N. D., Benke, P. J., Braun, J. T., Curry, C. J., Fernhoff, P. M., Grix, A. W., Lott, I. T., et al. (1985) · New England Journal of Medicine
Pregnancy and Medication ImpactPharmacological Effects and Toxicity Studies
Cited by 1,942
- Verified
Evolution of human-specific neural SRGAP2 genes by incomplete segmental duplication
Dennis, M. Y., Nuttle, X., Sudmant, P. H., Antonacci, F., Graves, T. A., Nefedov, M., Rosenfeld, J. A., Sajjadian, S., Malig, M., Kotkiewicz, H., et al. (2012) · Cell
Genomic variations and chromosomal abnormalitiesChromosomal and Genetic Variations
Cited by 407
- Verified
Tenascin-X deficiency is associated with Ehlers-Danlos syndrome
Burch, G. H., Gong, Y., Liu, W., Dettman, R. W., Curry, C. J., Smith, L., Miller, W. L., & Bristow, J. (1997) · Nature Genetics
Connective tissue disorders researchGenomics and Rare Diseases
Cited by 366
- Verified
Measurement of pesticides and other toxicants in amniotic fluid as a potential biomarker of prenatal exposure: a validation study
Bradman, A., Barr, D. B., Claus Henn, B. G., Drumheller, T., Curry, C., & Eskenazi, B. (2003) · Environmental Health Perspectives
Pesticide Exposure and ToxicityPesticide Residue Analysis and Safety
Cited by 258
- Verified
ACMG Practice Guideline: lack of evidence for MTHFR polymorphism testing
Hickey, S. E., Curry, C. J., & Toriello, H. V. (2013) · Genetics in Medicine
Folate and B Vitamins ResearchBlood Coagulation and Thrombosis Mechanisms
Cited by 175
- Verified
Deleterious, protein-altering variants in the transcriptional coregulator ZMYM3 in 27 individuals with a neurodevelopmental delay phenotype
Hiatt, S. M., Trajkova, S., Sebastiano, M. R., Partridge, E. C., Abidi, F. E., Anderson, A., Ansar, M., Antonarakis, S. E., Azadi, A., Bachmann-Gagescu, R., et al. (2023) · The American Journal of Human Genetics
Genetics and Neurodevelopmental DisordersGenomics and Rare Diseases
Cited by 21
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