P626: ImputePGTA: Accurate embryo genotyping and polygenic scoring from ultra-low-pass sequencing
Jeremy Li, Tobias Wolfram, Ivan Davidson, Justin Schleede et autres
0 citationsGenetics in Medicine Open
Justin Schleede
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20Publications signalées
277Citations signalées
1Affiliations récentes
Institutions déclarées
Domaines associés
Prenatal Screening and DiagnosticsGenomic variations and chromosomal abnormalitiesGenomics and Rare DiseasesDevelopmental Biology and Gene RegulationCancer Genomics and Diagnostics
Publications récentes
P737: HLA-ARC: An HLA-augmented Bayesian polygenic framework for type 1 diabetes risk prediction and embryo-level risk reduction modeling
Spencer Moore, Ivan Davidson, Jonathan Anomaly, Майер et autres
0 citationsGenetics in Medicine Open
ImputePGTA: accurate embryo genotyping and polygenic scoring from ultra-low-pass sequencing
Jeremiah H. Li, Tobias Wolfram, Justin Schleede, Jennifer A. Swift et autres
0 citationsmedRxiv
The first clinical validation of whole-genome screening on standard trophectoderm biopsies of preimplantation embryos
Yuntao Xia, M. Katz, Dhruva Chandramohan, Elan Bechor et autres
12 citationsF&S Reports
Genome-Wide Disease Screening of Early Human Embryos at Base-Pair Resolution
Yuntao Xia, Veronica Gonzalez-Pena, David Klein, Dhruva Chandramohan et autres
0 citationsResearch Square
First clinical validation of whole genome screening on standard trophectoderm biopsies of preimplantation embryos
Yuntao Xia, Willy Chertman, Dhruva Chandramohan, M. Katz et autres
3 citationsbioRxiv (Cold Spring Harbor Laboratory)
Eye, Ocular Adnexa, and Facial Manifestations of Tetrasomy 18p
Stephanie Saadeh‐Jackson, Kayla King, Hind Al Saif, Colleen Jackson‐Cook et autres
3 citationsJournal of Pediatric Ophthalmology & Strabismus
Standardizing the classification of recurrent copy number variants–incorporation of sub-clinical phenotype data for CNVs with reduced penetrance
John Herriges, Erica Andersen, Bradley P. Coe, Laura K. Conlin et autres
0 citationsMolecular Genetics and Metabolism
3. Standardizing recurrent copy number variant classification – From benign to reduced and high penetrance regions
Erica Andersen, John Herriges, Bradley P. Coe, Laura K. Conlin et autres
0 citationsCancer Genetics
Monosomy X rescue explains discordant NIPT results and leads to uniparental isodisomy
M. Katharine Rudd, Justin Schleede, Sabrina Williams, Kristy Lee et autres
9 citationsPrenatal Diagnosis
80: Chromosomal microarray analysis of over 45,000 prenatal patients: Significance and efficacy as a first tier diagnostic test
Stuart Schwartz, Romela Pasion, Huong Cabral, Rachel D. Burnside et autres
1 citationAmerican Journal of Obstetrics and Gynecology
Selective Advantage of the Recurrent Isodicentric Chromosome 20 in Myeloid Disease
Justin Schleede, Peter Papenhausen, Stuart Schwartz, Inder Gadi
0 citationsBlood
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