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Marsha Wheeler
Marsha Wheeler
Verified email at uw.edu
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Year
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
4422020
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
2822008
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
2812009
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
1372015
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
1222011
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
1012019
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
972001
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
952014
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
862016
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
682015
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
632012
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
612018
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
592019
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
592010
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
532018
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
472022
Inhibition of termite cellulases by carbohydrate-based cellulase inhibitors: Evidence from in vitro biochemistry and in vivo feeding studies
X Zhou, MM Wheeler, FM Oi, ME Scharf
Pesticide Biochemistry and Physiology 90 (1), 31-41, 2008
472008
The effect of omega-3 docosahexaenoic acid supplementation on gestational length: randomized trial of supplementation compared to nutrition education for increasing n-3 intake …
MA Harris, MS Reece, JA McGregor, JW Wilson, SM Burke, M Wheeler, ...
BioMed research international 2015, 2015
462015
Whole-genome sequencing association analysis of quantitative red blood cell phenotypes: The NHLBI TOPMed program
Y Hu, AM Stilp, CP McHugh, S Rao, D Jain, X Zheng, J Lane, ...
The American Journal of Human Genetics 108 (5), 874-893, 2021
442021
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
392022
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