Coriell Institute For Medical Research company information, Employees & Contact Information

Human iPSC Reprogramming Success: The Impact of Approaches and Source Materials Wiley Online Library

Elevated propionate and its association with neurological dysfunctions in propionic acidemia Frontiers

An updated protocol for the cost-effective and weekend-free culture of human induced pluripotent stem cells ScienceDirect.com

Star allele search: a pharmacogenetic annotation database and user-friendly search tool of publicly available 1000 Genomes Project biospecimens BMC Genomics

Development of genomic reference materials for Huntington disease genetic testing | Genetics in Medicine Nature

Jean-Pierre Issa, MD, Expert in Cancer Epigenetics, to Lead Coriell Institute for Medical Research as President and CEO | Newswise Newswise

NMDA receptors promote survival in somatosensory relay nuclei by inhibiting Bax-dependent developmental cell death PNAS

African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1 medRxiv

ursaPGx: a new R package to annotate pharmacogenetic star alleles using phased whole-genome sequencing data Frontiers

An African perspective on genetically diverse human induced pluripotent stem cell lines Nature

Allele-specific RNAi therapy corrects an extracellular matrix defect in Schuurs-Hoeijmakers syndrome ScienceDirect.com

Individuals with Slower Ibuprofen Metabolism Can Self-adjust Dosage | Newswise Newswise

MicroRNA-455-3p as a Potential Biomarker for Alzheimer's Disease: An Update Frontiers

African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in GBA1 Nature

A Novel Humanized Anti-Interleukin-6 Antibody HZ0408b With Anti-Rheumatoid Arthritis Therapeutic Potential Frontiers

A cryptic microdeletion del(12)(p11.21p11.23) within an unbalanced translocation t(7;12)(q21.13;q23.1) implicates new candidate loci for intellectual disability and Kallmann syndrome Nature

Validation and Utilization of a Clinical Next-Generation Sequencing Panel for Selected Cardiovascular Disorders Frontiers

Generation and expansion of highly pure motor neuron progenitors from human pluripotent stem cells Nature

ONT long-read WGS for variant discovery and orthogonal confirmation of short read WGS derived genetic variants in clinical genetic testing Frontiers

Long-Distance Phasing of a Tentative “Enhancer” Single-Nucleotide Polymorphism With CYP2D6 Star Allele Definitions Frontiers

Development and validation of a pharmacogenomics reporting workflow based on the illumina global screening array chip Frontiers

Validated WGS and WES protocols proved saliva-derived gDNA as an equivalent to blood-derived gDNA for clinical and population genomic analyses BMC Genomics

Extensive and deep sequencing of the Venter/HuRef genome for developing and benchmarking genome analysis tools Nature

Targeted nanopore sequencing using the Flongle device to identify mitochondrial DNA variants Nature

Human iPSC Reprogramming Success: The Impact of Approaches and Source Materials Wiley Online Library

Epigenetic DNA Methylation Profiling with MSRE: A Quantitative NGS Approach Using a Parkinson's Disease Test Case Frontiers

Comparison of three variant callers for human whole genome sequencing Nature

Tandem-genotypes : robust detection of tandem repeat expansions from long DNA reads Genome Biology

Role of ACE2 genetic polymorphisms in susceptibility to SARS-CoV-2 among highly exposed but non infected healthcare workers Taylor & Francis Online

Single-cell transcriptomics of human iPSC differentiation dynamics reveal a core molecular network of Parkinson’s disease Nature

Summer Research Programs For Driven High School Students Forbes

Joyce Coriell Obituary - Columbus, OH Dignity Memorial

Epigenetics and Genome Studies with the Coriell Institute's Dr. Jean-Pierre Issa | Teen Scientist WDIY

CD39 deletion exacerbates experimental murine colitis and human polymorphisms increase susceptibility to inflammatory bowel disease PNAS

Comparison of single cell sequencing data between two whole genome amplification methods on two sequencing platforms Nature

Modeling ALS with iPSCs Reveals that Mutant SOD1 Misregulates Neurofilament Balance in Motor Neurons ScienceDirect.com

Consequences of CYP2D6 Copy-Number Variation for Pharmacogenomics in Psychiatry Frontiers

High-throughput screen detects calcium signaling dysfunction in typical sporadic autism spectrum disorder Nature

MARILYN McGEORGE Obituary (2018) - Haddonfield, PA - The Philadelphia Inquirer Legacy obituary

Long-read sequencing reveals novel isoform-specific eQTLs and regulatory mechanisms of isoform expression medRxiv

Identification of hepta-histidine as a candidate drug for Huntington’s disease by in silico-in vitro- in vivo -integrated screens of chemical libraries Nature

Intragenic CFTR Duplication and 5T/12TG Variant in a Patient with Non-Classic Cystic Fibrosis Nature

Consanguinity in Centre d’Étude du Polymorphisme Humain (CEPH) pedigrees Nature

Developing a Sustainable Process to Provide Quality Control Materials for Genetic Testing Nature

Cannabis Genotyping – MCS Laboratories Modern Canna

A multiplex SNP assay for the dissection of human Y-chromosome haplogroup O representing the major paternal lineage in East and Southeast Asia Nature

Anthony D'Auria Obituary (2012) - 83, Brant Beach, NJ - Asbury Park Press Legacy obituary

Edmond Preston Obituary (2008) - Philadelphia, PA - The Philadelphia Inquirer Legacy obituary