| Liver from bone marrow in humans ND Theise, M Nimmakayalu, R Gardner, PB Illei, G Morgan, L Teperman, ... Hepatology 32 (1), 11-16, 2000 | 1917 | 2000 |
| Real-time quantitative RT-PCR of cyclin D1 mRNA in mantle cell lymphoma: comparison with FISH and immunohistochemistry P Hui*, JG Howe*, J Crouch, M Nimmakayalu, MB Qumsiyeh, G Tallini, ... Leukemia & lymphoma 44 (8), 1385-1394, 2003 | 291 | 2003 |
| Low copy repeats mediate distal chromosome 22q11. 2 deletions: sequence analysis predicts breakpoint mechanisms TH Shaikh, RJ O’Connor, ME Pierpont, J McGrath, AM Hacker, ... Genome research 17 (4), 482-491, 2007 | 156 | 2007 |
| Somatic mutation distributions in cancer genomes vary with three-dimensional chromatin structure KC Akdemir, VT Le, JM Kim, S Killcoyne, DA King, YP Lin, Y Tian, A Inoue, ... Nature genetics 52 (11), 1178-1188, 2020 | 112 | 2020 |
| Cloning and Characterization of Two Mouse Genes with Homology to the Yeast Sir2 Gene YH Yang, YH Chen, CY Zhang, MA Nimmakayalu, DC Ward, S Weissman Genomics 69 (3), 355-369, 2000 | 93 | 2000 |
| Microdeletion of 17q22q23.2 encompassing TBX2 and TBX4 in a patient with congenital microcephaly, thyroid duct cyst, sensorineural hearing loss, and … M Nimmakayalu, H Major, V Sheffield, DH Solomon, RJ Smith, SR Patil, ... American journal of medical genetics Part A 155 (2), 418-423, 2011 | 74 | 2011 |
| Characteristics of three homologous 202 genes (Ifi202a, Ifi202b, and Ifi202c) from the murine interferon-activatable gene 200 cluster H Wang, G Chatterjee, JJ Meyer, CJ Liu, NA Manjunath, P Bray-Ward, ... Genomics 60 (3), 281-294, 1999 | 69 | 1999 |
| A palindrome-driven complex rearrangement of 22q11. 2 and 8q24. 1 elucidated using novel technologies AL Gotter, MA Nimmakayalu, GR Jalali, AM Hacker, J Vorstman, DC Duffy, ... Genome research 17 (4), 470-481, 2007 | 67 | 2007 |
| A novel sequence-based approach to localize translocation breakpoints identifies the molecular basis of at (4; 22) MA Nimmakayalu, AL Gotter, TH Shaikh, BS Emanuel Human molecular genetics 12 (21), 2817-2825, 2003 | 66 | 2003 |
| Rapid detection of submicroscopic chromosomal rearrangements in children with multiple congenital anomalies using high density oligonucleotide arrays JE Ming, E Geiger, AC James, KL Ciprero, M Nimmakayalu, Y Zhang, ... Human mutation 27 (5), 467-473, 2006 | 53 | 2006 |
| High-resolution structural variant profiling of myelodysplastic syndromes by optical genome mapping uncovers cryptic aberrations of prognostic and therapeutic significance H Yang, G Garcia-Manero, K Sasaki, G Montalban-Bravo, Z Tang, Y Wei, ... Leukemia 36 (9), 2306-2316, 2022 | 52 | 2022 |
| Karyotype–phenotype insights from 11q14.1‐q23.2 interstitial deletions: FZD4 haploinsufficiency and exudative vitreoretinopathy in a patient with a complex … P Li, HZ Zhang, S Huff, M Nimmakayalu, M Qumsiyeh, J Yu, A Szekely, ... American Journal of Medical Genetics Part A 140 (24), 2721-2729, 2006 | 38 | 2006 |
| FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6 HZ Zhang, P Li, D Wang, S Huff, M Nimmakayalu, M Qumsiyeh, BR Pober American Journal of Medical Genetics Part A 124 (3), 280-287, 2004 | 36 | 2004 |
| An eight-gene hypoxia signature predicts survival in pancreatic cancer and is associated with an immunosuppressed tumor microenvironment R Abou Khouzam, SP Rao, GH Venkatesh, NA Zeinelabdin, S Buart, ... Frontiers in immunology 12, 680435, 2021 | 34 | 2021 |
| Apparent Germline Mosaicism for a Novel 19p13.13 Deletion Disrupting NFIX and CACNA1A M Nimmakayalu, VK Horton, B Darbro, SR Patil, H Alsayouf, ... American Journal of Medical Genetics Part A 161 (5), 1105-1109, 2013 | 30 | 2013 |
| A novel 4p16. 3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features AB Cyr, M Nimmakayalu, SQ Longmuir, SR Patil, KM Keppler‐Noreuil, ... American Journal of Medical Genetics Part A 155 (9), 2224-2228, 2011 | 29 | 2011 |
| Characterization of a cryptic 3.3 Mb deletion in a patient with a “balanced t (15; 22) translocation” using high density oligo array CGH and gene expression arrays MM Li, MA Nimmakayalu, D Mercer, HC Andersson, BS Emanuel American Journal of Medical Genetics Part A 146 (3), 368-375, 2008 | 29 | 2008 |
| Assignment1 of SYNJ1 to human chromosome 21q22. 2 and Synj12 to the murine homologous region on chromosome 16C3–4 by in situ hybridization O Cremona, M Nimmakayalu, C Haffner, P Bray-Ward, DC Ward, ... Cytogenetic and Genome Research 88 (1-2), 89-90, 2000 | 27 | 2000 |
| Simple method for preparation of fluor/hapten-labeled dUTP M Nimmakayalu, O Henegariu, DC Ward, P Bray-Ward Biotechniques 28 (3), 518-522, 2000 | 26 | 2000 |
| Genomic structure, cDNA mapping, and chromosomal localization of the mouse homeobox gene, Hex B Ghosh, HC Jacobs, LM Wiedemann, A Brown, FK Bedford, ... Mammalian genome 10, 1023-1025, 1999 | 22 | 1999 |
