| Mutations in the TRKA/NGF receptor gene in patients with congenital insensitivity to pain with anhidrosis Y Indo, M Tsuruta, Y Hayashida, MA Karim, K Ohta, T Kawano, ... Nature genetics 13 (4), 485-488, 1996 | 813 | 1996 |
| Identification and mutation analysis of the complete gene for Chediak–Higashi syndrome DL Nagle, MA Karim, EA Woolf, L Holmgren, P Bork, DJ Misumi, ... Nature genetics 14 (3), 307-311, 1996 | 615 | 1996 |
| Pantothenate kinase regulation of the intracellular concentration of coenzyme A CO Rock, RB Calder, MA Karim, S Jackowski Journal of Biological Chemistry 275 (2), 1377-1383, 2000 | 246 | 2000 |
| Apparent genotype–phenotype correlation in childhood, adolescent, and adult Chediak‐Higashi syndrome MA Karim, K Suzuki, K Fukai, J Oh, DL Nagle, KJ Moore, E Barbosa, ... American journal of medical genetics 108 (1), 16-22, 2002 | 205 | 2002 |
| Emerging biomarkers in autism spectrum disorder: a systematic review RE Frye, S Vassall, G Kaur, C Lewis, M Karim, D Rossignol Annals of translational medicine 7 (23), 2019 | 189 | 2019 |
| Overexpression of a mammalian ethanolamine-specific kinase accelerates the CDP-ethanolamine pathway A Lykidis, J Wang, MA Karim, S Jackowski Journal of Biological Chemistry 276 (3), 2174-2179, 2001 | 124 | 2001 |
| Gene structure, expression and identification of a new CTP: phosphocholine cytidylyltransferase β isoform M Karim, P Jackson, S Jackowski Biochimica et Biophysica Acta (BBA)-Molecular and Cell Biology of Lipids …, 2003 | 110 | 2003 |
| Maternal folate-related gene environment interactions and congenital heart defects CA Hobbs, MA Cleves, MA Karim, W Zhao, SL MacLeod Obstetrics & Gynecology 116 (2 Part 1), 316-322, 2010 | 103 | 2010 |
| The murine pantothenate kinase (Pank1) gene encodes two differentially regulated pantothenate kinase isozymes CO Rock, MA Karim, YM Zhang, S Jackowski Gene 291 (1-2), 35-43, 2002 | 102 | 2002 |
| Maternal genome-wide DNA methylation patterns and congenital heart defects S Chowdhury, SW Erickson, SL MacLeod, MA Cleves, P Hu, MA Karim, ... PloS one 6 (1), e16506, 2011 | 97 | 2011 |
| Mutations in the Chediak-Higashi Syndrome Gene (CHS1) Indicate Requirement for the Complete 3801 Amino Acid CHS Protein MA Karim, DL Nagle, HH Kandil, J Burger, KJ Moore, RA Spritz Human Molecular Genetics 6 (7), 1087-1089, 1997 | 88 | 1997 |
| PPARα controls the intracellular coenzyme A concentration via regulation of PANK1α gene expression1 G Ramaswamy, MA Karim, KG Murti, S Jackowski Journal of lipid research 45 (1), 17-31, 2004 | 85 | 2004 |
| Structure and organization of the humanTRKA gene encoding a high affinity receptor for nerve growth factor Y Indo, S Mardy, M Tsuruta, MA Karim, I Matsuda Japanese Journal of Human Genetics 42 (2), 343-351, 1997 | 76 | 1997 |
| Homozygosity mapping of the gene for Chediak-Higashi syndrome to chromosome 1q42-q44 in a segment of conserved synteny that includes the mouse beige locus (bg). K Fukai, J Oh, MA Karim, KJ Moore, HH Kandil, H Ito, J Bürger, RA Spritz American journal of human genetics 59 (3), 620, 1996 | 75 | 1996 |
| Disruption of CCTβ2 expression leads to gonadal dysfunction S Jackowski, JE Rehg, YM Zhang, J Wang, K Miller, P Jackson, MA Karim Molecular and cellular biology, 2004 | 72 | 2004 |
| Developmental regression and mitochondrial function in children with autism K Singh, IN Singh, E Diggins, SL Connors, MA Karim, D Lee, ... Annals of clinical and translational neurology 7 (5), 683-694, 2020 | 51 | 2020 |
| Variation within the gene encoding the upstream stimulatory factor 1 does not influence susceptibility to type 2 diabetes in samples from populations with replicated evidence … E Zeggini, CM Damcott, RL Hanson, MA Karim, NW Rayner, CJ Groves, ... Diabetes 55 (9), 2541-2548, 2006 | 46 | 2006 |
| Human ESP1/CRP2, a member of the LIM domain protein family: characterization of the cDNA and assignment of the gene locus to chromosome 14q32. 3 MA Karim, K Ohta, M Egashira, Y Jinno, N Niikawa, I Matsuda, Y Indo Genomics 31 (2), 167-176, 1996 | 32 | 1996 |
| Mitochondrial morphology is associated with respiratory chain uncoupling in autism spectrum disorder RE Frye, L Lionnard, I Singh, MA Karim, H Chajra, M Frechet, K Kissa, ... Translational Psychiatry 11 (1), 527, 2021 | 31 | 2021 |
| Analysis of FOXO1A as a candidate gene for type 2 diabetes MA Karim, RL Craig, X Wang, TC Hale, SC Elbein Molecular genetics and metabolism 88 (2), 171-177, 2006 | 31 | 2006 |