| A comprehensive analysis of 22q11 gene expression in the developing and adult brain TM Maynard, GT Haskell, AZ Peters, L Sikich, JA Lieberman, AS LaMantia Proceedings of the National Academy of Sciences 100 (24), 14433-14438, 2003 | 172 | 2003 |
| Retinoic acid signaling identifies a distinct precursor population in the developing and adult forebrain GT Haskell, AS LaMantia Journal of Neuroscience 25 (33), 7636-7647, 2005 | 107 | 2005 |
| Retinoic acid signaling at sites of plasticity in the mature central nervous system G Thompson Haskell, TM Maynard, RA Shatzmiller, AS Lamantia Journal of Comparative Neurology 452 (3), 228-241, 2002 | 96 | 2002 |
| 22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome TM Maynard, GT Haskell, JA Lieberman, AS LaMantia International Journal of Developmental Neuroscience 20 (3-5), 407-419, 2002 | 68 | 2002 |
| Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders GT Haskell, MC Adams, Z Fan, K Amin, RJ Guzman Badillo, L Zhou, ... Neurology: Genetics 4 (1), e212, 2018 | 59 | 2018 |
| Whole exome sequencing identifies truncating variants in nuclear envelope genes in patients with cardiovascular disease GT Haskell, BC Jensen, LA Samsa, D Marchuk, W Huang, C Skrzynia, ... Circulation: Cardiovascular Genetics 10 (3), e001443, 2017 | 44 | 2017 |
| RanBP1, a velocardiofacial/DiGeorge syndrome candidate gene, is expressed at sites of mesenchymal/epithelial induction TM Maynard, GT Haskell, N Bhasin, JM Lee, AA Gassman, JA Lieberman, ... Mechanisms of development 111 (1-2), 177-180, 2002 | 28 | 2002 |
| Sensitivity of whole exome sequencing in detecting infantile-and late-onset Pompe disease M Mori, G Haskell, Z Kazi, X Zhu, SM DeArmey, JL Goldstein, D Bali, ... Molecular genetics and metabolism 122 (4), 189-197, 2017 | 24 | 2017 |
| Limited influence of olanzapine on adult forebrain neural precursors in vitro JH Councill, ES Tucker, GT Haskell, TM Maynard, DW Meechan, ... Neuroscience 140 (1), 111-122, 2006 | 20 | 2006 |
| Current concepts in breast cancer genomics: an evidence based review by the CGC breast cancer working group KB Geiersbach, H Chen, R Emmadi, GT Haskell, X Lu, YJ Liu, ... Cancer Genetics 244, 11-20, 2020 | 10 | 2020 |
| Integrated Analysis of HER2 Copy Number by Cytogenomic Microarray in Breast Cancers With Nonclassical In Situ Hybridization Results GT Haskell, YJ Liu, H Chen, B Chen, RG Meyer, JA Yuhas, ... American journal of clinical pathology 149 (2), 135-147, 2018 | 5 | 2018 |
| Combination of exome sequencing and immune testing confirms Aicardi–Goutieres syndrome type 5 in a challenging pediatric neurology case GT Haskell, M Mori, C Powell, TJ Amrhein, GI Rice, L Bailey, N Strande, ... Molecular Case Studies 4 (5), a002758, 2018 | 4 | 2018 |
| Genetic complexity of mitral valve prolapse revealed by clinical and genetic evaluation of a large family GT Haskell, BC Jensen, C Skrzynia, T Pulikkotil, CR Tilley, Y Lu, ... The Journal of heart valve disease 26 (5), 569, 2017 | 3 | 2017 |
| P479: Mosaicism for genome wide homozygosity identified as an incidental finding in two healthy pregnant women G Haskell, H Askree, L Kline, QH Cabral, L Hasadri, I Gadi, S Schwartz Genetics in Medicine Open 1 (1), 2023 | 1 | 2023 |
| Utilization of a SNP microarray to detect uniparental disomy: Implications and outcomes A Arreola, G Haskell, I Gadi, A Penton, S Schwartz Genetics in Medicine 26 (12), 101275, 2024 | | 2024 |
| Prenatal detection of mosaicism for a genome wide uniparental disomy cell line in a cohort of patients: Implications and outcomes M Johansen, GT Haskell, A Arreola, C Riordan, IK Gadi, A Penton, ... Prenatal Diagnosis 44 (5), 586-594, 2024 | | 2024 |
| P592: Cytogenetic and microarray analysis of prenatally detected congenital heart defects (CHD): Diagnostic findings and variation among CHD subtypes S Schwartz, A Arreola, I Gadi, G Haskell, B Huang, J Knops, A Penton, ... Genetics in Medicine Open 2, 2024 | | 2024 |
| P571: Detection of isodisomy utilizing SNP microarray: Frequency, ascertainment, and implications S Molinari, N Williams, K Phillips, G Haskell, A Penton, I Gadi, A Arreola, ... Genetics in Medicine Open 2, 2024 | | 2024 |
| P140: A rare phenomenon: Double trisomy rescue detected during clinical SNP microarray testing A Penton, P Papenhausen, S Schwartz, A Vu, G Haskell Genetics in Medicine Open 2, 2024 | | 2024 |
| Chromosome 6p25 deletion syndrome: A case report and review of ophthalmic features H Le, E Jin, A Jewell, C Jackson‐Cook, GT Haskell, N Couser American Journal of Medical Genetics Part A 191 (6), 1639-1645, 2023 | | 2023 |
