Michael Sacher

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 15

Top Venues

Journal of inherited metabolic disease

Disease models & mechanisms

Traffic (Copenhagen, Denmark)

Brain : a journal of neurology

Concordia University

McGill University (BSC)

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

Affiliation History

Concordia University

Canada

Assistant/Associate (2012-2018)/Professor (2018-) :: Biology

Montreal Proteomics Network

Canada

Project Leader

Caprion Pharmaceuticals Inc

Canada

Senior Scientist

Yale University

United States

Associate Research Scientist :: Cell Biology

Yale University

United States

Postdoctoral Associate :: Cell Biology

Education History

McGill University

Canada

BSC :: Biochemistry

McGill University

Canada

PHD :: Biochemistry

Publications

Michael Sacher, Jay DeLoriea, Mahsa Mehranfar, Cody Casey, Aaliya Naaz, Chiara Gamberi
TANGO2 deficiency disease is predominantly caused by a lipid imbalance. Disease models & mechanisms 17 (6) (2024)
Erta Zykaj, Chelsea Abboud, Paria Asadi, Simane Warsame, Hashem Almousa, Miroslav P Milev, Brittany M Greco, Marcos López-Sánchez, Drago Bratkovic, Aashiq H Kachroo, Luis Alberto Pérez-Jurado, Michael Sacher
A Humanized Yeast Model for Studying TRAPP Complex Mutations; Proof-of-Concept Using Variants from an Individual with a TRAPPC1 -Associated Neurodevelopmental Syndrome. Cells 13 (17) (2024)
Michael Sacher, Jay DeLoriea, Mahsa Mehranfar, Cody Casey, Aaliya Naaz, Chiara Gamberi
TANGO2 deficiency disease is predominantly caused by a lipid imbalance. Disease models & mechanisms 17 (6) (2024)
Michael Sacher, Jay DeLoriea, Mahsa Mehranfar, Cody Casey, Aaliya Naaz, Chiara Gamberi
TANGO2 deficiency disease is predominantly caused by a lipid imbalance. Disease models & mechanisms 17 (6) (2024)
Michael Sacher, Jay DeLoriea, Mahsa Mehranfar, Cody Casey, Aaliya Naaz, Chiara Gamberi
TANGO2 deficiency disease is predominantly caused by a lipid imbalance. Disease models & mechanisms 17 (6) (2024)
Hashem Almousa, Sara A Lewis, Somayeh Bakhtiari, Sandra Hinz Nordlie, Alex Pagnozzi, Helen Magee, Stephanie Efthymiou, Jennifer A Heim, Patricia Cornejo, Maha S Zaki, Najwa Anwar, Shazia Maqbool, Fatima Rahman, Derek E Neilson, Anusha Vemuri, Sheng Chih Jin, Xiao-Ru Yang, Abolfazl Heidari, Koen van Gassen, Aurélien Trimouille, Christel Thauvin-Robinet, James Liu, Ange-Line Bruel, Hoda Tomoum, Mennatallah O Shata, Mais O Hashem, Mehran Beiraghi Toosi, Ehsan Ghayoor Karimiani, Gözde Yeşil, Lokesh Lingappa, Debangana Baruah, Farnoosh Ebrahimzadeh, Julien Van-Gils, Laurence Faivre, Mina Zamani, Hamid Galehdari, Saeid Sadeghian, Gholamreza Shariati, Rahema Mohammad, Jasper van der Smagt, Alya Qari, John B Vincent, A Micheil Innes, Ali Dursun, R Köksal Özgül, Halil Tuna Akar, Kaya Bilguvar, Cyril Mignot, Boris Keren, Claudia Raveli, Lydie Burglen, Alexandra Afenjar, Laura Donker Kaat, Marjon van Slegtenhorst, Fowzan Sami Alkuraya, Henry Houlden, Sergio Padilla-Lopez, Reza Maroofian, Michael Sacher, Michael C Kruer
TRAPPC6B biallelic variants cause a neurodevelopmental disorder with TRAPP II and trafficking disruptions. Brain : a journal of neurology (2023)
Paria Asadi, Miroslav P Milev, Djenann Saint-Dic, Chiara Gamberi, Michael Sacher
Vitamin B5, a coenzyme A precursor, rescues TANGO2 deficiency disease-associated defects in Drosophila and human cells. Journal of inherited metabolic disease 46 (2) (2022)
Paria Asadi, Miroslav P Milev, Djenann Saint-Dic, Chiara Gamberi, Michael Sacher
Vitamin B5, a coenzyme A precursor, rescues TANGO2 deficiency disease-associated defects in Drosophila and human cells. Journal of inherited metabolic disease (2022)
Paria Asadi, Miroslav P Milev, Djenann Saint-Dic, Chiara Gamberi, Michael Sacher
Vitamin B5, a coenzyme A precursor, rescues TANGO2 deficiency disease-associated defects in Drosophila and human cells. Journal of inherited metabolic disease 46 (2) (2022)
Lettie E Rawlins, Hashem Almousa, Shazia Khan, Stephan C Collins, Miroslav P Milev, Joseph S Leslie, Djenann Saint-Dic, Valeed Khan, Ana Maria Hincapie, Jacob O Day, Lucy McGavin, Christine Rowley, Gaurav V Harlalka, Valerie E Vancollie, Wasim Ahmad, Christopher J Lelliott, Asma Gul, Binnaz Yalcin, Andrew H Crosby, Michael Sacher, Andrew H Crosby
Biallelic variants in TRAPPC10 cause a microcephalic TRAPPopathy disorder in humans and mice. PLoS genetics 18 (3) (2022)
Paria Asadi, Miroslav P Milev, Djenann Saint-Dic, Chiara Gamberi, Michael Sacher
Vitamin B5, a Coenzyme A precursor, rescues TANGO2 deficiency disease-associated defects in Drosophila and human cells. Journal of inherited metabolic disease (2022)
Miroslav P Milev, Djenann Saint-Dic, Khashayar Zardoui, Thomas Klopstock, Christopher Law, Felix Distelmaier, Michael Sacher
The phenotype associated with variants in TANGO2 may be explained by a dual role of the protein in ER-to-Golgi transport and at the mitochondria. Journal of inherited metabolic disease 44 (2) (2020)
Daniela Stanga, Qingchuan Zhao, Miroslav P Milev, Djenann Saint-Dic, Cecilia Jimenez-Mallebrera, Michael Sacher
TRAPPC11 functions in autophagy by recruiting ATG2B-WIPI4/WDR45 to preautophagosomal membranes. Traffic (Copenhagen, Denmark) 20 (5) (2019)
Austin A Larson, Peter R Baker, Miroslav P Milev, Craig A Press, Ronald J Sokol, Mary O Cox, Jacqueline K Lekostaj, Aaron A Stence, Aaron D Bossler, Jennifer M Mueller, Keshika Prematilake, Thierry Fotsing Tadjo, Charles A Williams, Michael Sacher, Steven A Moore
TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophy. Skeletal muscle 8 (1) (2018)
Michael Sacher, Nassim Shahrzad, Hiba Kamel, Miroslav P Milev
TRAPPopathies: An emerging set of disorders linked to variations in the genes encoding transport protein particle (TRAPP)-associated proteins. Traffic (Copenhagen, Denmark) 20 (1) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

Michael Sacher