Michael F Wangler (Michael Wangler)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 18

Top Venues

Baylor College of Medicine

University of California San Diego (MSC)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Baylor College of Medicine Jul 01 2011

United States

Assistant Professor :: Molecular and Human Genetics

Education History

University of California San Diego Jul 02 2000 - Jul 01 2001

United States

MSC :: Biological Sciences

University of California San Diego - Jul 01 2000

United States

BSC :: Biological sciences

Publications

Michael F Wangler, Yu-Hsin Chao, Mary Roth, Ruth Welti, James A McNew
Drosophila Models Uncover Substrate Channeling Effects on Phospholipids and Sphingolipids in Peroxisomal Biogenesis Disorders. bioRxiv : the preprint server for biology (2024)
Dongxue Mao, Chaozhong Liu, Linhua Wang, Rami Ai-Ouran, Cole Deisseroth, Sasidhar Pasupuleti, Seon Young Kim, Lucian Li, Jill Anne Rosenfeld, Linyan Meng, Lindsay C Burrage, Michael F Wangler, Shinya Yamamoto, null null, Michael Santana, Victor Perez, Priyank Shukla, Christine M Eng, Brendan H Lee, Bo Yuan, Fan Xia, Hugo J Bellen, Pengfei Liu, Zhandong Liu
AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders. NEJM AI 1 (5) (2024)
Dongxue Mao, Chaozhong Liu, Linhua Wang, Rami Ai-Ouran, Cole Deisseroth, Sasidhar Pasupuleti, Seon Young Kim, Lucian Li, Jill Anne Rosenfeld, Linyan Meng, Lindsay C Burrage, Michael F Wangler, Shinya Yamamoto, null null, Michael Santana, Victor Perez, Priyank Shukla, Christine M Eng, Brendan H Lee, Bo Yuan, Fan Xia, Hugo J Bellen, Pengfei Liu, Zhandong Liu
AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders. NEJM AI 1 (5) (2024)
Michael F Wangler, Yu-Hsin Chao, Mary Roth, Ruth Welti, James A McNew
Drosophila Models Uncover Substrate Channeling Effects on Phospholipids and Sphingolipids in Peroxisomal Biogenesis Disorders. bioRxiv : the preprint server for biology (2024)
Dongxue Mao, Chaozhong Liu, Linhua Wang, Rami Ai-Ouran, Cole Deisseroth, Sasidhar Pasupuleti, Seon Young Kim, Lucian Li, Jill Anne Rosenfeld, Linyan Meng, Lindsay C Burrage, Michael F Wangler, Shinya Yamamoto, null null, Michael Santana, Victor Perez, Priyank Shukla, Christine M Eng, Brendan H Lee, Bo Yuan, Fan Xia, Hugo J Bellen, Pengfei Liu, Zhandong Liu
AI-MARRVEL - A Knowledge-Driven AI System for Diagnosing Mendelian Disorders. NEJM AI 1 (5) (2024)
Sharayu V Jangam, Lauren C Briere, Kristy L Jay, Jonathan C Andrews, Melissa A Walker, Lance H Rodan, Frances A High, null null, Shinya Yamamoto, David A Sweetser, Michael F Wangler
A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster. Genetics (2023)
Sharayu Jangam, Lauren C Briere, Kristy Jay, Jonathan C Andrews, Melissa A Walker, Lance H Rodan, Frances A High, null null, Shinya Yamamoto, David A Sweetser, Michael F Wangler
A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster . medRxiv : the preprint server for health sciences (2023)
Sharayu Jangam, Lauren C Briere, Kristy Jay, Jonathan C Andrews, Melissa A Walker, Lance H Rodan, Frances A High, null null, Shinya Yamamoto, David A Sweetser, Michael F Wangler
A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster . medRxiv : the preprint server for health sciences (2023)
Cara P Ford, Rebecca O Littlejohn, Ryan J German, Blake Vuocolo, Jose Aceves, Liesbeth Vossaert, Nichole Owen, Michael F Wangler, Carrie A Schmid, null null
Precision therapy for a medically actionable ATP1A3 variant from a genomic medicine program in an underserved population. Molecular genetics & genomic medicine (2023)
J Michael Harnish, Lucian Li, Sanja Rogic, Guillaume Poirier-Morency, Seon-Young Kim, null null, Kym M Boycott, Michael F Wangler, Hugo J Bellen, Philip Hieter, Paul Pavlidis, Zhandong Liu, Shinya Yamamoto
ModelMatcher: A scientist-centric online platform to facilitate collaborations between stakeholders of rare and undiagnosed disease research. Human mutation 43 (6) (2022)
Joshua Manor, Hyunglok Chung, Pranjali K Bhagwat, Michael F Wangler
ABCD1 and X-linked adrenoleukodystrophy: A disease with a markedly variable phenotype showing conserved neurobiology in animal models. Journal of neuroscience research (2021)
Katharina V Schulze, Neil A Hanchard, Michael F Wangler
Biases in arginine codon usage correlate with genetic disease risk. Genetics in medicine : official journal of the American College of Medical Genetics 22 (8) (2020)
Nurit Assia Batzir, Pranjali Kishor Bhagwat, Austin Larson, Zeynep Coban Akdemir, Maciej Bagłaj, Leon Bofferding, Katherine B Bosanko, Skander Bouassida, Bert Callewaert, Ashley Cannon, Yazmin Enchautegui Colon, Adolfo D Garnica, Margaret H Harr, Sandra Heck, Anna C E Hurst, Shalini N Jhangiani, Bertrand Isidor, Rebecca O Littlejohn, Pengfei Liu, Pilar Magoulas, Helen Mar Fan, Ronit Marom, Scott McLean, Marjan M Nezarati, Kimberly M Nugent, Michael B Petersen, Maria L Rocha, Elizabeth Roeder, Robert Smigiel, Ian Tully, James Weisfeld-Adams, Katerina O Wells, null null, Jennifer E Posey, James R. Lupski, Arthur L Beaudet, Michael F Wangler
Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy. Human mutation 41 (3) (2019)
Magdalena Koczkowska, Tom Callens, Yunjia Chen, Alicia Gomes, Alesha D Hicks, Angela Sharp, Eric Johns, Kim Armfield Uhas, Linlea Armstrong, Katherine Armstrong Bosanko, Dusica Babovic-Vuksanovic, Laura Baker, Donald G Basel, Mario Bengala, James T Bennett, Chelsea Chambers, Lola K Clarkson, Maurizio Clementi, Fanny M Cortés, Mitch Cunningham, M Daniela D'Agostino, Martin B Delatycki, Maria C Digilio, Laura Dosa, Silvia Esposito, Stephanie Fox, Mary-Louise Freckmann, Christine Fauth, Teresa Giugliano, Sandra Giustini, Allison Goetsch, Yael Goldberg, Robert S Greenwood, Cristin Griffis, Karen W Gripp, Punita Gupta, Eric Haan, Rachel K Hachen, Tamara L Haygarth, Concepción Hernández-Chico, Katelyn Hodge, Robert J Hopkin, Louanne Hudgins, Sandra Janssens, Kory Keller, Geraldine Kelly-Mancuso, Aaina Kochhar, Bruce R Korf, Andrea M Lewis, Jan Liebelt, Angie Lichty, Robert H Listernick, Michael J Lyons, Isabelle Maystadt, Mayra Martinez Ojeda, Carey McDougall, Lesley K McGregor, Daniela Melis, Nancy Mendelsohn, Malgorzata J M Nowaczyk, June Ortenberg, Karin Panzer, John G Pappas, Mary Ella Pierpont, Giulio Piluso, Valentina Pinna, Eniko K Pivnick, Dinel A Pond, Cynthia M Powell, Caleb Rogers, Noa Ruhrman Shahar, S Lane Rutledge, Veronica Saletti, Sarah A Sandaradura, Claudia Santoro, Ulrich A Schatz, Allison Schreiber, Daryl A Scott, Elizabeth A Sellars, Ruth Sheffer, Elizabeth Siqveland, John M Slopis, Rosemarie Smith, Alberto Spalice, David W Stockton, Haley Streff, Amy Theos, Gail E Tomlinson, Grace Tran, Pamela L Trapane, Eva Trevisson, Nicole J Ullrich, Jenneke Van den Ende, Samantha A Schrier Vergano, Stephanie E Wallace, Michael F Wangler, David D Weaver, Kaleb H Yohay, Elaine Zackai, Jonathan Zonana, Vickie Zurcher, Kathleen B M Claes, Marica Eoli, Yolanda Martin, Katharina Wimmer, Alessandro De Luca, Eric Legius, Ludwine M Messiaen
Clinical spectrum of individuals with pathogenic NF1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype-phenotype study in neurofibromatosis type 1. Human mutation 41 (1) (2019)
Nurit Assia Batzir, Pranjali K Bhagwat, Tanya N Eble, Pengfei Liu, Christine M Eng, Sarah H Elsea, Laurie A Robak, Fernando Scaglia, Alica M Goldman, Shweta U Dhar, Michael F Wangler
De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures. Cold Spring Harbor molecular case studies 5 (3) (2019)
Xi Luo, Jill Anne Rosenfeld, Shinya Yamamoto, Tamar Harel, Zhongyuan Zuo, Melissa Hall, Klaas J Wierenga, Matthew T Pastore, Dennis Bartholomew, Mauricio R Delgado, Joshua Rotenberg, Richard Alan Lewis, Lisa Emrick, Carlos A Bacino, Mohammad K Eldomery, Zeynep C Akdemir, Fan Xia, Yaping Yang, Seema R Lalani, Timothy Lotze, James R Lupski, Brendan H Lee, Hugo J Bellen, Michael F Wangler, null null
Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially. PLoS genetics 13 (7) (2017)
Michael F Wangler, Yu-Hsin Chao, Vafa Bayat, Nikolaos Giagtzoglou, Abhijit Babaji Shinde, Nagireddy Putluri, Cristian Coarfa, Taraka Donti, Brett H Graham, Joseph E Faust, James A McNew, Ann Moser, Marco Sardiello, Myriam Baes, Hugo J Bellen
Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse. PLoS genetics 13 (6) (2017)
Michael F Wangler, Shinya Yamamoto, Hsiao-Tuan Chao, Jennifer E Posey, Monte Westerfield, John H Postlethwait, null null, Philip Hieter, Kym M Boycott, Philippe M Campeau, Hugo J Bellen
Model Organisms Facilitate Rare Disease Diagnosis and Therapeutic Research. Genetics 207 (1) (2017)
Michael F Wangler, Shinya Yamamoto, Hugo J Bellen
Fruit flies in biomedical research. Genetics 199 (3) (2015)

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Publication Activity (10 Years)

Top Topics

Top Venues

Michael F Wangler (Michael Wangler)