Seuraa
Marsha Wheeler
Marsha Wheeler
Vahvistettu sähköpostiosoite verkkotunnuksessa uw.edu
Nimike
Viittaukset
Viittaukset
Vuosi
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
5772020
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
2832008
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
2772009
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
2162024
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
1482015
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
1332011
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
1232019
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
1162014
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
982001
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
962016
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
792019
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
702018
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
692015
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
662023
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
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
612018
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
612010
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
602022
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
572022
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
552023
Järjestelmä ei voi suorittaa toimenpidettä nyt. Yritä myöhemmin uudelleen.
Artikkelit 1–20