Erin Loring
Yale University(US)
Publications by Year
Research Areas
Craniofacial Disorders and Treatments, Hormonal Regulation and Hypertension, Ion Transport and Channel Regulation, Cleft Lip and Palate Research, Skin and Cellular Biology Research
Most-Cited Works
- → Somatic and germline CACNA1D calcium channel mutations in aldosterone-producing adenomas and primary aldosteronism(2013)607 cited
- → Mutation of NLRC4 causes a syndrome of enterocolitis and autoinflammation(2014)505 cited
- → L-Histidine Decarboxylase and Tourette's Syndrome(2010)363 cited
- → Recurrent gain of function mutation in calcium channel CACNA1H causes early-onset hypertension with primary aldosteronism(2015)347 cited
- → CLCN2 chloride channel mutations in familial hyperaldosteronism type II(2018)258 cited
- → Histidine Decarboxylase Deficiency Causes Tourette Syndrome: Parallel Findings in Humans and Mice(2014)252 cited
- → Two locus inheritance of non-syndromic midline craniosynostosis via rare SMAD6 and common BMP2 alleles(2016)195 cited
- → De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus(2018)157 cited
- → Multilineage somatic activating mutations in HRAS and NRAS cause mosaic cutaneous and skeletal lesions, elevated FGF23 and hypophosphatemia(2013)135 cited
- → De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis(2017)100 cited