Michael F. Wangler
Michael F. Wangler
Baylor College of Medicine
Verified email at bcm.tmc.edu - Homepage
Title
Cited by
Cited by
Year
A drosophila genetic resource of mutants to study mechanisms underlying human genetic diseases
S Yamamoto, M Jaiswal, WL Charng, T Gambin, E Karaca, G Mirzaa, ...
Cell 159 (1), 200-214, 2014
2822014
Association between Beckwith-Wiedemann syndrome and assisted reproductive technology: a case series of 19 patients
AS Chang, KH Moley, M Wangler, AP Feinberg, MR DeBaun
Fertility and sterility 83 (2), 349-354, 2005
2682005
Use of exome sequencing for infants in intensive care units: ascertainment of severe single-gene disorders and effect on medical management
L Meng, M Pammi, A Saronwala, P Magoulas, AR Ghazi, F Vetrini, ...
JAMA pediatrics 171 (12), e173438-e173438, 2017
2312017
Racial disparity in the frequency of recurrence of preterm birth
ZAF Kistka, L Palomar, KA Lee, SE Boslaugh, MF Wangler, FS Cole, ...
American journal of obstetrics and gynecology 196 (2), 131. e1-131. e6, 2007
2252007
Peroxisome biogenesis disorders in the Zellweger spectrum: an overview of current diagnosis, clinical manifestations, and treatment guidelines
NE Braverman, GV Raymond, WB Rizzo, AB Moser, ME Wilkinson, ...
Molecular genetics and metabolism 117 (3), 313-321, 2016
1522016
Effect of genetic diagnosis on patients with previously undiagnosed disease
K Splinter, DR Adams, CA Bacino, HJ Bellen, JA Bernstein, ...
New england journal of medicine 379 (22), 2131-2139, 2018
1452018
Lessons learned from additional research analyses of unsolved clinical exome cases
MK Eldomery, Z Coban-Akdemir, T Harel, JA Rosenfeld, T Gambin, ...
Genome medicine 9 (1), 1-15, 2017
1382017
Fruit flies in biomedical research
MF Wangler, S Yamamoto, HJ Bellen
Genetics 199 (3), 639-653, 2015
1352015
Model organisms facilitate rare disease diagnosis and therapeutic research
MF Wangler, S Yamamoto, HT Chao, JE Posey, M Westerfield, ...
Genetics 207 (1), 9-27, 2017
1072017
The undiagnosed diseases network: accelerating discovery about health and disease
RB Ramoni, JJ Mulvihill, DR Adams, P Allard, EA Ashley, JA Bernstein, ...
The American Journal of Human Genetics 100 (2), 185-192, 2017
1042017
MARRVEL: integration of human and model organism genetic resources to facilitate functional annotation of the human genome
J Wang, R Al-Ouran, Y Hu, SY Kim, YW Wan, MF Wangler, S Yamamoto, ...
The American Journal of Human Genetics 100 (6), 843-853, 2017
1012017
Heterozygous De Novo and Inherited Mutations in the Smooth Muscle Actin (ACTG2) Gene Underlie Megacystis-Microcolon-Intestinal Hypoperistalsis Syndrome
MF Wangler, C Gonzaga-Jauregui, T Gambin, S Penney, T Moss, ...
PLoS genetics 10 (3), e1004258, 2014
1012014
A syndromic neurodevelopmental disorder caused by de novo variants in EBF3
HT Chao, M Davids, E Burke, JG Pappas, JA Rosenfeld, AJ McCarty, ...
The American Journal of Human Genetics 100 (1), 128-137, 2017
692017
Mother’s genome or maternally-inherited genes acting in the fetus influence gestational age in familial preterm birth
J Plunkett, MF Feitosa, M Trusgnich, MF Wangler, L Palomar, ZAF Kistka, ...
Human heredity 68 (3), 209-219, 2009
692009
Loss of nardilysin, a mitochondrial co-chaperone for α-ketoglutarate dehydrogenase, promotes mTORC1 activation and neurodegeneration
WH Yoon, H Sandoval, S Nagarkar-Jaiswal, M Jaiswal, S Yamamoto, ...
Neuron 93 (1), 115-131, 2017
652017
Fibrochondrogenesis results from mutations in the COL11A1 type XI collagen gene
SW Tompson, CA Bacino, NP Safina, MB Bober, VK Proud, T Funari, ...
The American Journal of Human Genetics 87 (5), 708-712, 2010
602010
De novo truncating mutations in AHDC1 in individuals with syndromic expressive language delay, hypotonia, and sleep apnea
F Xia, MN Bainbridge, TY Tan, MF Wangler, AE Scheuerle, EH Zackai, ...
The American Journal of Human Genetics 94 (5), 784-789, 2014
592014
Loss-of-function variants in MYLK cause recessive megacystis microcolon intestinal hypoperistalsis syndrome
D Halim, E Brosens, F Muller, MF Wangler, AL Beaudet, JR Lupski, ...
The American Journal of Human Genetics 101 (1), 123-129, 2017
482017
Missense variants in the middle domain of DNM1L in cases of infantile encephalopathy alter peroxisomes and mitochondria when assayed in Drosophila
YH Chao, LA Robak, F Xia, MK Koenig, A Adesina, CA Bacino, F Scaglia, ...
Human molecular genetics 25 (9), 1846-1856, 2016
482016
Factors associated with preterm delivery in mothers of children with Beckwith–Wiedemann syndrome: a case cohort study from the BWS registry
MF Wangler, AS Chang, KH Moley, AP Feinberg, MR DeBaun
American Journal of Medical Genetics Part A 134 (2), 187-191, 2005
462005
The system can't perform the operation now. Try again later.
Articles 1–20