Inherited causes of clonal haematopoiesis in 97,691 whole genomes AG Bick, JS Weinstock, SK Nandakumar, CP Fulco, EL Bao, SM Zekavat, ... Nature 586 (7831), 763-768, 2020 | 577 | 2020 |
RNA interference in the termite Reticulitermes flavipes through ingestion of double-stranded RNA X Zhou, MM Wheeler, FM Oi, ME Scharf Insect Biochemistry and Molecular Biology 38 (8), 805-815, 2008 | 283 | 2008 |
Parallel metatranscriptome analyses of host and symbiont gene expression in the gut of the termite Reticulitermes flavipes A Tartar, MM Wheeler, X Zhou, MR Coy, DG Boucias, ME Scharf Biotechnology for biofuels 2, 1-19, 2009 | 277 | 2009 |
Genomic data in the all of us research program Biobank, Mayo Blegen Ashley L. 18 Wirkus Samantha J. 18 Wagner Victoria A ... Nature 627 (8003), 340-346, 2024 | 216 | 2024 |
De novo mutations in NALCN cause a syndrome characterized by congenital contractures of the limbs and face, hypotonia, and developmental delay JX Chong, MJ McMillin, KM Shively, AE Beck, CT Marvin, JR Armenteros, ... The American Journal of Human Genetics 96 (3), 462-473, 2015 | 148 | 2015 |
Mechanisms of stable lipid loss in a social insect SA Ament, QW Chan, MM Wheeler, SE Nixon, SP Johnson, ... Journal of Experimental Biology 214 (22), 3808-3821, 2011 | 133 | 2011 |
Stargazer: a software tool for calling star alleles from next-generation sequencing data using CYP2D6 as a model S Lee, MM Wheeler, K Patterson, S McGee, R Dalton, EL Woodahl, ... Genetics in medicine 21 (2), 361-372, 2019 | 123 | 2019 |
Diet-dependent gene expression in honey bees: honey vs. sucrose or high fructose corn syrup MM Wheeler, GE Robinson Scientific reports 4 (1), 5726, 2014 | 116 | 2014 |
The omega-3 story:: Nutritional prevention of preterm birth and other adverse pregnancy outcomes JA McGregor, KGD Allen, MA Harris, M Reece, M Wheeler, JI French, ... Obstetrical & gynecological survey 56 (5), S1-S13, 2001 | 98 | 2001 |
MECR mutations cause childhood-onset dystonia and optic atrophy, a mitochondrial fatty acid synthesis disorder G Heimer, JM Kerätär, LG Riley, S Balasubramaniam, E Eyal, ... The American Journal of Human Genetics 99 (6), 1229-1244, 2016 | 96 | 2016 |
Calling star alleles with stargazer in 28 pharmacogenes with whole genome sequences S Lee, MM Wheeler, KE Thummel, DA Nickerson Clinical Pharmacology & Therapeutics 106 (6), 1328-1337, 2019 | 79 | 2019 |
MACF1 mutations encoding highly conserved zinc-binding residues of the GAR domain cause defects in neuronal migration and axon guidance WB Dobyns, KA Aldinger, GE Ishak, GM Mirzaa, AE Timms, ME Grout, ... The American Journal of Human Genetics 103 (6), 1009-1021, 2018 | 70 | 2018 |
Autosomal-dominant multiple pterygium syndrome is caused by mutations in MYH3 JX Chong, LC Burrage, AE Beck, CT Marvin, MJ McMillin, KM Shively, ... The American Journal of Human Genetics 96 (5), 841-849, 2015 | 69 | 2015 |
Beyond the exome: what’s next in diagnostic testing for Mendelian conditions MH Wojcik, CM Reuter, S Marwaha, M Mahmoud, MH Duyzend, ... The American Journal of Human Genetics 110 (8), 1229-1248, 2023 | 66 | 2023 |
New meta-analysis tools reveal common transcriptional regulatory basis for multiple determinants of behavior SA Ament, CA Blatti, C Alaux, MM Wheeler, AL Toth, Y Le Conte, GJ Hunt, ... Proceedings of the National Academy of Sciences 109 (26), E1801-E1810, 2012 | 63 | 2012 |
Genetic analysis of CHARGE syndrome identifies overlapping molecular biology A Moccia, A Srivastava, JM Skidmore, JA Bernat, M Wheeler, JX Chong, ... Genetics in medicine 20 (9), 1022-1029, 2018 | 61 | 2018 |
Characterization of four esterase genes and esterase activity from the gut of the termite Reticulitermes flavipes MM Wheeler, MR Tarver, MR Coy, ME Scharf Archives of Insect Biochemistry and Physiology: Published in Collaboration …, 2010 | 61 | 2010 |
Centers for Mendelian Genomics: A decade of facilitating gene discovery SM Baxter, JE Posey, NJ Lake, N Sobreira, JX Chong, S Buyske, EE Blue, ... Genetics in Medicine 24 (4), 784-797, 2022 | 60 | 2022 |
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed MA Taub, MP Conomos, R Keener, KR Iyer, JS Weinstock, LR Yanek, ... Cell Genomics 2 (1), 2022 | 57 | 2022 |
Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis JS Weinstock, J Gopakumar, BB Burugula, MM Uddin, N Jahn, JA Belk, ... Nature 616 (7958), 755-763, 2023 | 55 | 2023 |