Risa Peoples
Marquette University(US)
Publications by Year
Research Areas
Williams Syndrome Research, Genomic variations and chromosomal abnormalities, Diverse Scientific and Economic Studies, Human auditory perception and evaluation, Electrocatalysts for Energy Conversion
Most-Cited Works
- Molecular definition of the chromosome 7 deletion in Williams syndrome and parent-of-origin effects on growth.(1996)
- → A Physical Map, Including a BAC/PAC Clone Contig, of the Williams-Beuren Syndrome–Deletion Region at 7q11.23(2000)180 cited
- → A novel human homologue of the Drosophila frizzled wnt receptor gene binds wingless protein and is in the Williams syndrome deletion at 7q11.23(1997)161 cited
- The gene for replication factor C subunit 2 (RFC2) is within the 7q11.23 Williams syndrome deletion.(1996)
- → Identification of GTF2IRD1, a putative transcription factor within the Williams-Beuren syndrome deletion at 7q11.23(1999)60 cited
- → Receptor mutations and haplotypes in growth hormone receptor deficiency: a global survey and identification of the Ecuadorean E180splice mutation in an oriental Jewish patient(1994)56 cited
- → Identification of the WBSCR9 gene, encoding a novel transcriptional regulator, in the Williams-Beuren syndrome deletion at 7q11.23(1998)55 cited
- → Hemizygosity at the insulin-like growth factor I eceptor (IGF1R) locus and growth failure in the ring chromosome 15 syndrome(1995)53 cited
- → Genes for the CPE Receptor (CPETR1) and the Human Homolog of RVP1 (CPETR2) Are Localized within the Williams–Beuren Syndrome Deletion(1998)51 cited
- → Role of membrane GM1 on early neuronal membrane actions of Aβ during onset of Alzheimer's disease(2017)35 cited