Author details

Full Name

Brynn Levy

Affiliation

ORCID

Career Start Year

1997

Papers

127

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37301971	Implementation of Nanopore sequencing as a pragmatic workflow for copy number variant confirmation in the clinic.		2023
36302597	Genomic Disorders in CKD across the Lifespan.	J Am Soc Nephrol	2023
36417763	Optical genome mapping in acute myeloid leukemia: a multicenter evaluation.	Blood Adv	2023
37761828	3' UTR Deletion of <i>FBXO28</i> in a Patient with Brain Abnormalities and Developmental Delay.	Genes (Basel)	2023
37595579	Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies.	Am J Hum Genet	2023
36828597	Multisite Assessment of Optical Genome Mapping for Analysis of Structural Variants in Constitutional Postnatal Cases.	J Mol Diagn	2023
36809055	Integration of a Cross-Ancestry Polygenic Model With Clinical Risk Factors Improves Breast Cancer Risk Stratification.		2023
35241116	3q27.1 microdeletion causes prenatal and postnatal growth restriction and neurodevelopmental abnormalities.	Molecular Cytogenetics	2022
36070716	Rapid Nanopore Sequencing-Based Screen for Aneuploidy in Reproductive Care.	N Engl J Med	2022
35928455	Case Report: Prenatal Identification of a <i>De Novo</i> Mosaic Neocentric Marker Resulting in 13q31.1â¿¿qter Tetrasomy in a Mildly Affected Girl.	Front Genet	2022
35314819	Whole-genome risk prediction of common diseases in human preimplantation embryos.	Nat Med	2022
35036860	Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19.	iScience	2022
35167654	Guiding the global evolution of cytogenetic testing for hematologic malignancies.	Blood	2022
33597122	Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.	J Am Soc Nephrol	2021
34282301	Clinical and genomic characterization of 8p cytogenomic disorders.	Genet Med	2021
33720449	Chromosomal mosaicism: Origins and clinical implications in preimplantation and prenatal diagnosis.	Prenatal Diagnosis	2021
32597540	The 2019 Malcolm Ferguson-Smith Young Investigator Award.	Prenat Diagn	2020
32054310	A rapid and simple bead-bashing-based method for genomic DNA extraction from mammalian tissue.	Biotechniques	2020
30712878	Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study.	Lancet	2019
31785788	Validation Studies for Single Circulating Trophoblast Genetic Testing as a Form of Noninvasive Prenatal Diagnosis.	Am J Hum Genet	2019
30506199	Prenatal Diagnosis Using Chromosomal SNP Microarrays.	Methods in Molecular Biology	2019
30506194	Assessment of Maternal Cell Contamination in Prenatal Samples by Quantitative Fluorescent PCR (QF-PCR).	Methods in Molecular Biology	2019
30506193	DNA Extraction from Various Types of Prenatal Specimens.	Methods in Molecular Biology	2019
30506187	Traditional Prenatal Diagnosis: Past to Present.	Methods in Molecular Biology	2019
30593668	In case you missed it: The prenatal diagnosis editors bring you the most significant advances of 2018.	Prenat Diagn	2019
30578417	The copy number variation landscape of congenital anomalies of the kidney and urinary tract.	Nat Genet	2019
30816350	Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.	Nat Genet	2019
31414475	The 2018 Malcolm Ferguson-Smith Young Investigator Award.	Prenat Diagn	2019
30673135	Are all chromosome microarrays the same? What clinicians need to know.	Prenatal Diagnosis	2019
31001805	High-resolution genomic alterations in Barrett's metaplasia of patients who progress to esophageal dysplasia and adenocarcinoma.	Int J Cancer	2019
29322541	In case you missed it: The Prenatal Diagnosis editors bring you the most significant advances of 2017.	Prenat Diagn	2018
30357877	Reliable detection of subchromosomal deletions and duplications using cell-based noninvasive prenatal testing.	Prenat Diagn	2018
29952009	The 2017 Malcolm Ferguson-Smith Young Investigator Award.	Prenat Diagn	2018
29447663	Prenatal diagnosis by chromosomal microarray analysis.	Fertil Steril	2018
29474437	Validation of a SNP-based non-invasive prenatal test to detect the fetal 22q11.2 deletion in maternal plasma samples.	PLoS ONE	2018
29428286	The Use of Chromosomal Microarray Analysis in Prenatal Diagnosis.	Obstet Gynecol Clin North Am	2018
29416564	Identification of novel genomic imbalances in Saudi patients with congenital heart disease.	Molecular Cytogenetics	2018
28260531	Defining the diverse spectrum of inversions, complex structural variation, and chromothripsis in the morbid humanÂ genome.	Genome Biol	2017
28618411	Prevalence and Physical Distribution of SRY in the Gonads of a Woman with Turner Syndrome: Phenotypic Presentation, Tubal Formation, and Malignancy Risk.	Horm Res Paediatr	2017
28357155	Analytical and Clinical Validity Study of FirstStepDx PLUS: A Chromosomal Microarray Optimized for Patients with Neurodevelopmental Conditions.	PLoS Curr	2017
29053959	Restoration of Replication Fork Stability in BRCA1- and BRCA2-Deficient Cells by Inactivation of SNF2-Family Fork Remodelers.	Mol Cell	2017
29063499	At the dawn of personalized reproductive medicine: opportunities and challenges with incorporating multigene panel testing into fertility care.		2017
27941249	Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndrome.	Journal of Clinical Investigation	2017
28205301	In case you missed it: the Prenatal Diagnosis editors bring you the most significant advances of 2016.	Prenat Diagn	2017
27841880	The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.	Nat Genet	2017
27789403	Induced pluripotent stem cells (iPSC) created from skin fibroblasts of patients with Prader-Willi syndrome (PWS) retain the molecular signature of PWS.	Stem Cell Research	2016
27248180	The genetic landscape of dural marginal zone lymphomas.	Oncotarget	2016
27381265	The 2015 Malcolm Ferguson-Smith Young Investigator Award.	Prenat Diagn	2016
27235911	Chromosomal Microarrays for the Prenatal Detection of Microdeletions and Microduplications.	Clin Lab Med	2016
26853494	Genome-wide analysis of abdominal and pleural malignant mesothelioma with DNA arrays reveals both common and distinct regions of copy number alteration.	Cancer Biology and Therapy	2016