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Genetics

D-Index
66
Citations
18724
World Ranking
2596
National Ranking
1151

Overview

Bernice E. Morrow is affiliated with Albert Einstein College of Medicine in the United States. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, as well as Medicine. Within these broad fields, their work focuses on subfields such as Molecular Biology, Epidemiology, Pulmonary and Respiratory Medicine, Genetics, and Electrical and Electronic Engineering.

The research topics that define their scientific contributions include congenital heart defects research, congenital heart disease studies, coronary artery anomalies, genomic variations and chromosomal abnormalities, genetic associations and epidemiology, tracheal and airway disorders, and single-cell and spatial transcriptomics.

Bernice E. Morrow has authored numerous peer-reviewed papers, with several notable publications including:

  • Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome, 2020, Nature Medicine
  • Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion, 2020, Molecular Psychiatry
  • Single cell multi-omic analysis identifies a Tbx1-dependent multilineage primed population in murine cardiopharyngeal mesoderm, 2021, Nature Communications
  • Single-cell transcriptomics uncovers a non-autonomous Tbx1-dependent genetic program controlling cardiac neural crest cell development, 2023, Nature Communications
  • Optical mapping of the 22q11.2DS region reveals complex repeat structures and preferred locations for non-allelic homologous recombination (NAHR), 2020, Scientific Reports

The frequent co-authors that have collaborated with Bernice E. Morrow include:

  • Donna M. McDonald-McGinn
  • Beverly S. Emanuel
  • Elaine H. Zackai
  • Deyou Zheng
  • Anne S. Bassett

Their research has appeared in several publication venues, with frequent publications in:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Genes
  • Molecular Psychiatry
  • Nature Communications
  • Developmental Biology

Best Publications

  • 22q11.2 deletion syndrome

    Donna M. McDonald-McGinn;Kathleen E. Sullivan;Bruno Marino;Nicole Philip

  • The DNA sequence of human chromosome 22

    I. Dunham;N. Shimizu;B. A. Roe;S. Chissoe

  • TBX1 Is Responsible for Cardiovascular Defects in Velo-Cardio-Facial/DiGeorge Syndrome

    Sandra Merscher;Birgit Funke;Jonathan A. Epstein;Joerg Heyer

  • Schizophrenia susceptibility associated with interstitial deletions of chromosome 22q11

    M Karayiorgou;M A Morris;B Morrow;R J Shprintzen

  • Meiotic Pachytene Arrest in MLH1-Deficient Mice

    Winfried Edelmann;Paula E Cohen;Michael Kane;Kirkland Lau

  • A Common Molecular Basis for Rearrangement Disorders on Chromosome 22q11

    Lisa Edelmann;Raj K. Pandita;Elizabeth Spiteri;Birgit Funke

  • Psychotic illness in patients diagnosed with velo-cardio-facial syndrome and their relatives

    Ann E. Pulver;Gerald Nestadt;Rosalie Goldberg;Robert J. Shprintzen

  • Bipolar spectrum disorders in patients diagnosed with velo-cardio-facial syndrome: does a hemizygous deletion of chromosome 22q11 result in bipolar affective disorder?

    Demitri F. Papolos;Gianni L. Faedda;Sabine Veit;Rosalie Goldberg

  • Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndrome.

    Lisa Edelmann;Raj K. Pandita;Bernice E. Morrow

  • Molecular Definition of 22q11 Deletions in 151 Velo-Cardio-Facial Syndrome Patients

    C. Carlson;H. Sirotkin;R. Pandita;R. Goldberg;R. Goldberg

  • Association of codon 108/158 catechol-O-methyltransferase gene polymorphism with the psychiatric manifestations of velo-cardio-facial syndrome

    Herbert M. Lachman;Bernice Morrow;Robert Shprintzen;Sabine Veit

  • VEGF: a modifier of the del22q11 (DiGeorge) syndrome?

    Ingeborg Stalmans;Diether Lambrechts;Frederik De Smet;Sandra Jansen

  • Abraham's Children in the Genome Era: Major Jewish Diaspora Populations Comprise Distinct Genetic Clusters with Shared Middle Eastern Ancestry

    Gil Atzmon;Li Hao;Itsik Pe'er;Christopher Velez

  • Molecular definition of the 22q11 deletions in velo-cardio-facial syndrome.

    Bernice Morrow;Rosalie Goldberg;Christine Carlson;Ruchira Das Gupta

  • Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome

    Twila M. Yobb;Martin J. Somerville;Lionel Willatt;Helen V. Firth

  • Genomic disorders on 22q11.

    Heather E. McDermid;Bernice E. Morrow

  • Full spectrum of malformations in velo-cardio-facial syndrome/DiGeorge syndrome mouse models by altering Tbx1 dosage

    Jun Liao;Lazaros Kochilas;Sonja Nowotschin;Jelena S. Arnold

  • AT-Rich Palindromes Mediate the Constitutional t(11;22) Translocation

    L. Edelmann;L. Edelmann;E. Spiteri;K. Koren;V. Pulijaal

  • Tbx1 affects asymmetric cardiac morphogenesis by regulating Pitx2 in the secondary heart field.

    Sonja Nowotschin;Jun Liao;Philip J. Gage;Jonathan A. Epstein

  • Suppression of neural fate and control of inner ear morphogenesis by Tbx1.

    Steven Raft;Sonja Nowotschin;Jun Liao;Bernice E. Morrow

Frequent Co-Authors

Donna M. McDonald-McGinn
Donna M. McDonald-McGinn Children's Hospital of Philadelphia
Beverly S. Emanuel
Beverly S. Emanuel Children's Hospital of Philadelphia
Raju Kucherlapati
Raju Kucherlapati Harvard University
Elaine H. Zackai
Elaine H. Zackai Children's Hospital of Philadelphia
Anne S. Bassett
Anne S. Bassett University of Toronto
Wendy R. Kates
Wendy R. Kates SUNY Upstate Medical University
Birgit Funke
Birgit Funke Harvard University
Doron Gothelf
Doron Gothelf Tel Aviv University
Raj K. Pandita
Raj K. Pandita Houston Methodist
Peter J. Scambler
Peter J. Scambler University College London

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