| The 5th edition of the World Health Organization classification of haematolymphoid tumours: myeloid and histiocytic/dendritic neoplasms JD Khoury, E Solary, O Abla, Y Akkari, R Alaggio, JF Apperley, R Bejar, ... leukemia 36 (7), 1703-1719, 2022 | 1638 | 2022 |
| The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies C Redin, H Brand, RL Collins, T Kammin, E Mitchell, JC Hodge, ... Nature genetics 49 (1), 36-45, 2017 | 306 | 2017 |
| Rare deletions at the neurexin 3 locus in autism spectrum disorder AK Vaags, AC Lionel, D Sato, MK Goodenberger, QP Stein, S Curran, ... The American Journal of Human Genetics 90 (1), 133-141, 2012 | 256 | 2012 |
| Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures AC Lionel, AK Vaags, D Sato, MJ Gazzellone, EB Mitchell, HY Chen, ... Human molecular genetics 22 (10), 2055-2066, 2013 | 183 | 2013 |
| Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes AC Lionel, K Tammimies, AK Vaags, JA Rosenfeld, JW Ahn, D Merico, ... Human molecular genetics 23 (10), 2752-2768, 2014 | 176 | 2014 |
| TFE3 rearrangements in adult renal cell carcinoma: clinical and pathologic features with outcome in a large series of consecutively treated patients WR Sukov, JC Hodge, CM Lohse, BC Leibovich, RH Thompson, ... The American journal of surgical pathology 36 (5), 663-670, 2012 | 161 | 2012 |
| A cross-disorder dosage sensitivity map of the human genome RL Collins, JT Glessner, E Porcu, M Lepamets, R Brandon, C Lauricella, ... Cell 185 (16), 3041-3055. e25, 2022 | 149 | 2022 |
| ALK alterations in adult renal cell carcinoma: frequency, clinicopathologic features and outcome in a large series of consecutively treated patients WR Sukov, JC Hodge, CM Lohse, MK Akre, BC Leibovich, RH Thompson, ... Modern Pathology 25 (11), 1516-1525, 2012 | 144 | 2012 |
| Genetic heterogeneity among uterine leiomyomata: insights into malignant progression JC Hodge, CC Morton Human molecular genetics 16 (R1), R7-R13, 2007 | 127 | 2007 |
| Identification of single gene deletions at 15q13.3: further evidence that CHRNA7 causes the 15q13.3 microdeletion syndrome phenotype N Hoppman‐Chaney, K Wain, PR Seger, DW Superneau, JC Hodge Clinical genetics 83 (4), 345-351, 2013 | 113 | 2013 |
| High-grade endometrial stromal sarcomas: a clinicopathologic study of a group of tumors with heterogenous morphologic and genetic features AP Sciallis, PP Bedroske, JK Schoolmeester, WR Sukov, GL Keeney, ... The American journal of surgical pathology 38 (9), 1161-1172, 2014 | 93 | 2014 |
| Molecular cytogenetic analysis for TFE3 rearrangement in Xp11. 2 renal cell carcinoma and alveolar soft part sarcoma: validation and clinical experience with 75 cases JC Hodge, KE Pearce, X Wang, AE Wiktor, AM Oliveira, PT Greipp Modern Pathology 27 (1), 113-127, 2014 | 75 | 2014 |
| Requirement of RhoA activity for increased nuclear factor κB activity and PC-3 human prostate cancer cell invasion JC Hodge, J Bub, S Kaul, A Kajdacsy-Balla, PF Lindholm Cancer research 63 (6), 1359-1364, 2003 | 74 | 2003 |
| Disruption of MBD5 contributes to a spectrum of psychopathology and neurodevelopmental abnormalities JC Hodge, E Mitchell, V Pillalamarri, TL Toler, F Bartel, HM Kearney, ... Molecular psychiatry 19 (3), 368-379, 2014 | 67 | 2014 |
| Lysophosphatidic acid stimulates PC‐3 prostate cancer cell matrigel invasion through activation of RhoA and NF‐κB activity YS Hwang, JC Hodge, N Sivapurapu, PF Lindholm Molecular Carcinogenesis: Published in cooperation with the University of …, 2006 | 65 | 2006 |
| Expression profiling of uterine leiomyomata cytogenetic subgroups reveals distinct signatures in matched myometrium: transcriptional profiling of the t (12; 14) and evidence in … JC Hodge, TM Kim, JM Dreyfuss, P Somasundaram, NC Christacos, ... Human molecular genetics 21 (10), 2312-2329, 2012 | 63 | 2012 |
| Reciprocal deletion and duplication at 2q23. 1 indicates a role for MBD5 in autism spectrum disorder SV Mullegama, JA Rosenfeld, C Orellana, BWM Van Bon, S Halbach, ... European Journal of Human Genetics 22 (1), 57-63, 2014 | 60 | 2014 |
| Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele JC Hodge, K T. Cuenco, KL Huyck, P Somasundaram, CIM Panhuysen, ... Human genetics 125, 257-263, 2009 | 59 | 2009 |
| Uterine cellular leiomyomata with chromosome 1p deletions represent a distinct entity JC Hodge, KE Pearce, AC Clayton, FA Taran, EA Stewart American journal of obstetrics and gynecology 210 (6), 572. e1-572. e7, 2014 | 57 | 2014 |
| Paired-duplication signatures mark cryptic inversions and other complex structural variation H Brand, RL Collins, C Hanscom, JA Rosenfeld, V Pillalamarri, MR Stone, ... The American Journal of Human Genetics 97 (1), 170-176, 2015 | 53 | 2015 |
