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Items: 4

1.
Unraveling the functional role of the orphan solute carrier, SLC22A24 in the transport of steroid conjugates through metabolomic and genome-wide association studies
Sook Wah Yee, Adrian Stecula, Huan-Chieh Chien, Ling Zou, Elena V. Feofanova, Marjolein van Borselen, Kit Wun Kathy Cheung, Noha A. Yousri, Karsten Suhre, Jason M. Kinchen, Eric Boerwinkle, Roshanak Irannejad, Bing Yu, Kathleen M. Giacomini
PLoS Genet. 2019 Sep; 15(9): e1008208. Published online 2019 Sep 25. doi: 10.1371/journal.pgen.1008208
PMCID:
PMC6760779
AbstractArticlePDF–4.1M
2.
Genome-Wide Association Study of Maternal and Inherited Loci for Conotruncal Heart Defects
A. J. Agopian, Laura E. Mitchell, Joseph Glessner, Angela D. Bhalla, Anshuman Sewda, Hakon Hakonarson, Elizabeth Goldmuntz
PLoS One. 2014; 9(5): e96057. Published online 2014 May 6. doi: 10.1371/journal.pone.0096057
PMCID:
PMC4011736
AbstractArticlePDF–1.2M
3.
Identification of a novel MYOC variant in a Hispanic family with early-onset primary open-angle glaucoma with elevated intraocular pressure
June Criscione, Weizhen Ji, Lauren Jeffries, James M. McGrath, Scott Soloway, Lajos Pusztai, Saquib Lakhani
Cold Spring Harb Mol Case Stud. 2019 Dec; 5(6): a004374. doi: 10.1101/mcs.a004374
PMCID:
PMC6913140
AbstractArticlePDF–1.6M
4.
Discovery of rare ancestry-specific variants in the fetal genome that confer risk of preterm premature rupture of membranes (PPROM) and preterm birth
Bhavi P. Modi, Hardik I. Parikh, Maria E. Teves, Rewa Kulkarni, Jiang Liyu, Roberto Romero, Timothy P. York, Jerome F. Strauss, III
BMC Med Genet. 2018; 19: 181. Published online 2018 Oct 5. doi: 10.1186/s12881-018-0696-4
PMCID:
PMC6173941
AbstractArticlePDF–383K

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