| Clinical exome sequencing for fetuses with ultrasound abnormalities and a suspected Mendelian disorder EA Normand, A Braxton, S Nassef, PA Ward, F Vetrini, W He, V Patel, ... Genome medicine 10, 1-14, 2018 | 141 | 2018 |
| Clinical exome sequencing reveals locus heterogeneity and phenotypic variability of cohesinopathies B Yuan, J Neira, D Pehlivan, T Santiago-Sim, X Song, J Rosenfeld, ... Genetics in Medicine 21 (3), 663-675, 2019 | 61 | 2019 |
| Validation studies for single circulating trophoblast genetic testing as a form of noninvasive prenatal diagnosis L Vossaert, Q Wang, R Salman, AK McCombs, V Patel, C Qu, MA Mancini, ... The American Journal of Human Genetics 105 (6), 1262-1273, 2019 | 53 | 2019 |
| De novo missense variants in TRAF7 cause developmental delay, congenital anomalies, and dysmorphic features MJ Tokita, CA Chen, D Chitayat, E Macnamara, JA Rosenfeld, ... The American Journal of Human Genetics 103 (1), 154-162, 2018 | 44 | 2018 |
| Neuropsychological, neurovirological and neuroimmune aspects of abnormal GABAergic transmission in HIV infection T Buzhdygan, J Lisinicchia, V Patel, K Johnson, V Neugebauer, ... Journal of Neuroimmune Pharmacology 11, 279-293, 2016 | 34 | 2016 |
| Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease–associated loci for BAFopathies CA Chen, J Lattier, W Zhu, J Rosenfeld, L Wang, TM Scott, H Du, V Patel, ... Genetics in Medicine 24 (2), 364-373, 2022 | 15 | 2022 |
| Early circulating tumor DNA dynamics as a pan‐tumor biomarker for long‐term clinical outcome in patients treated with durvalumab and tremelimumab M Kansara, N Bhardwaj, S Thavaneswaran, C Xu, JK Lee, LB Chang, ... Molecular Oncology 17 (2), 298-311, 2023 | 7 | 2023 |
| Cell-based Noninvasive Prenatal Testing Enables Highly Sensitive Genomic Copy Number Analysis R Salman, L Vossaert, Q Wang, S Qdaisat, X Zhuo, E Normand, C Shaw, ... Annals of Clinical & Laboratory Science 48 (3), 2018 | | 2018 |
| The Utility of Clinical Exome Sequencing for Anomalous Fetuses with Suspected Mendelian Disorders N 1, 2 A. Braxton 1, SN 1, CQ 2, VP 2, 2 L. Meng 1, 2 P. Liu 1, 2 F. Xia 1, ... American College of Medical Genetics and Genomics, 2018 | | 2018 |
| Enhanced Detection of Uniparental Disomy (UPD) and Copy Number Variations (CNVs) with Delineation of Parental Origin for Clinical Trio Exome Cases YY Pengfei Liu, Hongzheng Dai, Weimin Bi, Ignatia Van den Veyver, Samantha ... American College of Medical Genetics and Genomics, 2018 | | 2018 |
| Data accumulated from clinical exome sequencing reveal the locus heterogeneity of cohesinopathies at its mild end of phenotypic spectrum Annual Clinical Genetics Meeting, 2018 | | 2018 |
| Intensity of suppression linked with shifting compartmentalization of CNS HIV DNA DLK Benjamin B. Gelman, Joshua G. Lisinicchia, Lalita D. Singh, Vipulkumar N ... Conference on retroviruses and opportunistic infections 68, 2017 | | 2017 |
| New generation of cancer treatment: Immunotherapy SGT Birju M Mehta, Vipul Kumar Patel Journal of Genetics and Molecular Biology 1 (1), 2017 | | 2017 |
| IRF4 Transcription Factor Associated With Integrated HIV DNA in Brain Macrophages DLK Benjamin B. Gelman1, Joshua G. Lisinicchia1, Tetyana P. Buzhdygan1 ... Conference on retroviruses and opportunistic infections 61, 2015 | | 2015 |
| High expression of interleukin 10 and interferon regulatory factor 4 are correlated with integrated HIV DNA in brain neocortex B Gelman, J Lisinicchia, T Buzhdygan, V Patel, T Clement, D Kolson, ... JOURNAL OF NEUROVIROLOGY 19, S31-S32, 2013 | | 2013 |
| Comprehensive survey ofGABAergic neural transmission in HIV infection reveals correlation with anomalies in the neurovascular unit and dopamine receptor expression in frontal … T Buzhdygan, J Lisinicchia, V Patel, T Clement, K Johnson, K Jennings, ... JOURNAL OF NEUROVIROLOGY 19, S16-S17, 2013 | | 2013 |
| Decreased GABAergic markers in HIV-associated neurocognitive disorders BG T. BUZHDYGAN, T. CHEN, J. LISINICCHIA, V. PATEL, J. CHANDARANA Society for Neuroscience, 2012 | | 2012 |
| Clinical validation and implementation of whole genome sequencing in molecular diagnostics of Mendelian disorders 2 P. Liu 1, 2 B. Yuan 1, JS 2, VN 2, ND 2, CJW 2, BH 2, MS 2, CYC 2, ... American Society of Human Genetics,2019, 0 | | |
Ignatia Van den VeyverProfessor, Baylor College of MedicineVerified email at bcm.edu
