G. Haskell

发表

Current concepts in breast cancer genomics: An evidence based review by the CGC breast cancer working group.

R. Emmadi, Hui Chen, Yajuan J. Liu, 2020, Cancer genetics.

Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease.

E. Cirulli, C. Rehder, D. Bali, 2017, Molecular genetics and metabolism.

Genetic Complexity of Mitral Valve Prolapse Revealed by Clinical and Genetic Evaluation of a Large Family.

Christian R. Tilley, E. Lange, J. Berg, 2017, The Journal of heart valve disease.

Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders

Christian R. Tilley, J. Berg, Michael C. Adams, 2018, Neurology: Genetics.

A comprehensive analysis of 22q11 gene expression in the developing and adult brain

J. Lieberman, A. LaMantia, T. Maynard, 2003, Proceedings of the National Academy of Sciences of the United States of America.

22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome

J. Lieberman, A. LaMantia, T. Maynard, 2002, International Journal of Developmental Neuroscience.

Combination of exome sequencing and immune testing confirms Aicardi–Goutières syndrome type 5 in a challenging pediatric neurology case

Jonathan S. Berg, James P. Evans, Karen E. Weck, 2018, Cold Spring Harbor molecular case studies.

Limited influence of olanzapine on adult forebrain neural precursors in vitro

R. Hamer, J. Lieberman, A. LaMantia, 2006, Neuroscience.

Retinoic Acid Signaling Identifies a Distinct Precursor Population in the Developing and Adult Forebrain

A. LaMantia, G. Haskell, 2005, The Journal of Neuroscience.

Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease

Christian R. Tilley, J. Berg, K. Wilhelmsen, 2017, Circulation. Cardiovascular genetics.

RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction

J. Lieberman, A. LaMantia, T. Maynard, 2002, Mechanisms of Development.

Whole Genome Sequencing in the Molecular Pathology Laboratory

J. Berg, G. Haskell, Gloria T. Haskell, 2017 .

Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features

C. Jackson-Cook, N. Couser, A. Jewell, 2023, American journal of medical genetics. Part A.

Integrated Analysis of HER2 Copy Number by Cytogenomic Microarray in Breast Cancers With Nonclassical In Situ Hybridization Results

Hui Chen, Yajuan J. Liu, Beiyun Chen, 2018, American journal of clinical pathology.