C. Gallagher

发表

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

J. Cook, A. Morris, A. Auton, 2019, Nature Communications.

Genome-wide association analysis identifies 27 novel loci associated with uterine leiomyomata revealing common genetic origins with endometriosis

J. Cook, A. Morris, R. Cantor, 2018, bioRxiv.

Clinical, pathologic, cytogenetic, and molecular profiling in self-identified black women with uterine leiomyomata.

C. Morton, B. Quade, Z. Ordulu, 2018, Cancer genetics.

Genetic Association Studies in Uterine Fibroids: Risk Alleles Presage the Path to Personalized Therapies

C. Morton, C. S. Gallagher, C. Gallagher, 2016, Seminars in Reproductive Medicine.

Investigating the shared genetic architecture of uterine leiomyoma and breast cancer: A genome-wide cross-trait analysis.

P. Kraft, C. Morton, Jiayuan Li, 2022, American journal of human genetics.

Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations

Stephane E. Castel, Anne-Katrin Emde, T. Merriman, 2021, BMC Genomics.

Specific correction of a splice defect in brain by nutritional supplementation.

M. Hims, M. Leyne, J. Mull, 2011, Human molecular genetics.

A multi-stage genome-wide association study of uterine fibroids in African Americans

Janina M. Jeff, D. Reich, D. Hinds, 2017, Human Genetics.

Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity

Jeffrey J. Beck, Zachary F. Gerring, H. Stefánsson, 2023, Human reproduction.

A comprehensive genome-wide cross-trait analysis of sexual factors and uterine leiomyoma

Xueyao Wu, Xunying Zhao, Xia Jiang, 2024, PLoS genetics.