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Gloria T. Haskell, Ph.D. - Publications

Affiliations: 
2004 University of North Carolina, Chapel Hill, Chapel Hill, NC 
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5/13 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2006 Councill JH, Tucker ES, Haskell GT, Maynard TM, Meechan DW, Hamer RM, Lieberman JA, LaMantia AS. Limited influence of olanzapine on adult forebrain neural precursors in vitro. Neuroscience. 140: 111-22. PMID 16564641 DOI: 10.1016/J.Neuroscience.2006.02.014  0.583
2005 Haskell GT, LaMantia AS. Retinoic acid signaling identifies a distinct precursor population in the developing and adult forebrain. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 25: 7636-47. PMID 16107650 DOI: 10.1523/Jneurosci.0485-05.2005  0.575
2003 Maynard TM, Haskell GT, Peters AZ, Sikich L, Lieberman JA, LaMantia AS. A comprehensive analysis of 22q11 gene expression in the developing and adult brain. Proceedings of the National Academy of Sciences of the United States of America. 100: 14433-8. PMID 14614146 DOI: 10.1073/Pnas.2235651100  0.68
2002 Maynard TM, Haskell GT, Lieberman JA, LaMantia AS. 22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome. International Journal of Developmental Neuroscience : the Official Journal of the International Society For Developmental Neuroscience. 20: 407-19. PMID 12175881 DOI: 10.1016/S0736-5748(02)00050-3  0.657
2002 Maynard TM, Haskell GT, Bhasin N, Lee JM, Gassman AA, Lieberman JA, LaMantia AS. RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction. Mechanisms of Development. 111: 177-80. PMID 11804793 DOI: 10.1016/S0925-4773(01)00616-5  0.673
Low-probability matches (unlikely to be authored by this person)
2023 Le H, Jin E, Jewell A, Jackson-Cook C, Haskell GT, Couser N. Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features. American Journal of Medical Genetics. Part A. PMID 36941760 DOI: 10.1002/ajmg.a.63186  0.238
2018 Haskell GT, Mori M, Powell C, Amrhein TJ, Rice GI, Bailey L, Strande N, Weck KE, Evans JP, Berg JS, Kishnani P. Combination of exome sequencing and immune testing confirms Aicardi-Goutières syndrome type 5 in a challenging pediatric neurology case. Cold Spring Harbor Molecular Case Studies. 4. PMID 30275001 DOI: 10.1101/mcs.a002758  0.143
2017 Haskell GT, Jensen BC, Samsa LA, Marchuk D, Huang W, Skrzynia C, Tilley C, Seifert BA, Rivera-Muñoz EA, Koller B, Wilhelmsen KC, Liu J, Alhosaini H, Weck KE, Evans JP, et al. Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease. Circulation. Cardiovascular Genetics. 10. PMID 28611029 DOI: 10.1161/CIRCGENETICS.116.001443  0.136
2017 Haskell GT, Jensen BC, Skrzynia C, Pulikkotil T, Tilley CR, Lu Y, Marchuk DS, Ann Samsa L, Wilhelmsen KC, Lange E, Patterson C, Evans JP, Berg JS. Genetic Complexity of Mitral Valve Prolapse Revealed by Clinical and Genetic Evaluation of a Large Family. The Journal of Heart Valve Disease. 26: 569-580. PMID 29762926  0.13
2018 Haskell GT, Liu YJ, Chen H, Chen B, Meyer RG, Yuhas JA, Geiersbach KB. Integrated Analysis of HER2 Copy Number by Cytogenomic Microarray in Breast Cancers With Nonclassical In Situ Hybridization Results. American Journal of Clinical Pathology. 149: 135-147. PMID 29385416 DOI: 10.1093/ajcp/aqx143  0.084
2018 Haskell GT, Adams MC, Fan Z, Amin K, Guzman Badillo RJ, Zhou L, Bizon C, Chahin N, Greenwood RS, Milko LV, Shiloh-Malawsky Y, Crooks KR, Strande N, Tennison M, Tilley CR, et al. Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders. Neurology. Genetics. 4: e212. PMID 29417091 DOI: 10.1212/Nxg.0000000000000212  0.077
2017 Mori M, Haskell G, Kazi Z, Zhu X, DeArmey SM, Goldstein JL, Bali D, Rehder C, Cirulli ET, Kishnani PS. Sensitivity of whole exome sequencing in detecting infantile- and late-onset Pompe disease. Molecular Genetics and Metabolism. PMID 29122469 DOI: 10.1016/J.Ymgme.2017.10.008  0.065
2020 Geiersbach KB, Chen H, Emmadi R, Haskell GT, Lu X, Liu YJ, Swisshelm K. Current concepts in breast cancer genomics: An evidence based review by the CGC breast cancer working group. Cancer Genetics. 244: 11-20. PMID 32087595 DOI: 10.1016/J.Cancergen.2020.02.002  0.047
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