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Trials|January 20, 2018
The Apathy in Dementia Methylphenidate Trial 2 (ADMET 2): study protocol for a randomized controlled trialRoberta W Scherer, Lea Drye, Jacobo Mintzer, et al.BMC Ophthalmology|November 23, 2006
Development and validation of a computerized expert system for evaluation of automated visual fields from the Ischemic Optic Neuropathy Decompression TrialSteven E Feldon, Lori Levin, Roberta W Scherer, et al.BMC Medical Genomics|February 19, 2022
GeneTerpret: a customizable multilayer approach to genomic variant prioritization and interpretationRoozbeh Manshaei, Sean DeLong, Veronica Andric, et al.Proceedings of the National Academy of Sciences of the United States of America|May 17, 2006
Hotspots for copy number variation in chimpanzees and humansGeorge H Perry, Joelle Tchinda, Sean D McGrath, et al.Psychiatric Genetics|May 23, 2008
A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpointsJohn B Vincent, Sanaa Choufani, Shin-ichi Horike, et al.Scientific Reports|September 16, 2017
Oxytocin Receptor Polymorphisms are Differentially Associated with Social Abilities across Neurodevelopmental DisordersDanielle A Baribeau, Annie Dupuis, Tara A Paton, et al.Nature Genetics|September 6, 2000
Mutations in ATP6N1B, encoding a new kidney vacuolar proton pump 116-kD subunit, cause recessive distal renal tubular acidosis with preserved hearingA N Smith, J Skaug, K A Choate, et al.Clinical Genetics|November 23, 2016
Compound heterozygous mutations in the IFT140 gene cause Opitz trigonocephaly C syndrome in a patient with typical features of a ciliopathyC Peña-Padilla, C R Marshall, S Walker, et al.The Journal of Biological Chemistry|September 13, 1996
Cloning and characterization of PDK4 on 7q21.3 encoding a fourth pyruvate dehydrogenase kinase isoenzyme in humanJ Rowles, S W Scherer, T Xi, et al.Genomics|February 12, 1998
Characterization of the gene encoding human sarcolipin (SLN), a proteolipid associated with SERCA1: absence of structural mutations in five patients with Brody diseaseA Odermatt, P E Taschner, S W Scherer, et al.Pageof 88