Frazier, Ann E.; Compton, Alison G.; Kishita, Yoshihito; Hock, Daniella H.; Welch, AnneMarie E.; Amarasekera, Sumudu S. C.; Rius, Rocio; Formosa, Luke E.; Imai-Okazaki, Atsuko; Francis, David; Wang, Min; Lake, Nicole J.; Tregoning, Simone; Jabbari, Jafar S.; Lucattini, Alexis; Nitta, Kazuhiro R.; Ohtake, Akira; Murayama, Kei; Amor, David J.; McGillivray, George; Wong, Flora Y.; van der Knaap, Marjo S.; Vermeulen, R. Jeroen; Wiltshire, Esko J.; Fletcher, Janice M.; Lewis, Barry; Baynam, Gareth; Ellaway, Carolyn; Balasubramaniam, Shanti; Bhattacharya, Kaustuv; Freckmann, Mary-Louise; Arbuckle, Susan; Rodriguez, Michael; Taft, Ryan J.; Sadedin, Simon; Cowley, Mark J.; Minoche, Andre E.; Calvo, Sarah E.; Mootha, Vamsi K.; Ryan, Michael T.; Okazaki, Yasushi; Stroud, David A.; Simons, Cas; Christodoulou, John; Thorburn, David R.

MitoCarta3.0: an updated mitochondrial proteome now with sub-organelle localization and pathway annotations

MitoCarta3.0: 具有亚细胞器定位和途径注释的更新的线粒体蛋白质组

NUCLEIC ACIDS RESEARCH

IF13.1

2020-11-11797

OAAI

Rath, Sneha; Sharma, Rohit; Gupta, Rahul; Ast, Tslil; Chan, Connie; Durham, Timothy J.; Goodman, Russell P.; Grabarek, Zenon; Haas, Mary E.; Hung, Wendy H. W.; Joshi, Pallavi R.; Jourdain, Alexis A.; Kim, Sharon H.; Kotrys, Anna, V; Lam, Stephanie S.; McCoy, Jason G.; Meisel, Joshua D.; Miranda, Maria; Panda, Apekshya; Patgiri, Anupam; Rogers, Robert; Sadre, Shayan; Shah, Hardik; Skinner, Owen S.; To, Tsz-Leung; Walker, Melissa A.; Wang, Hong; Ward, Patrick S.; Wengrod, Jordan; Yuan, Chen-Ching; Calvo, Sarah E.; Mootha, Vamsi K.

A patient with homozygous nonsense variants in two Leigh syndrome disease genes: Distinguishing a dual diagnosis from a hypomorphic protein-truncating variant

HUMAN MUTATION

IF3.7

2019-04-137

OAAI

GeNets: a unified web platform for network-based genomic analyses

NATURE METHODS

IF32.1

2018-06-1841

OAAI

Early loss of mitochondrial complex I and rewiring of glutathione metabolism in renal oncocytoma

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2018-06-1875

OAAI

Spatiotemporal compartmentalization of hepatic NADH and NADPH metabolism

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2018-05-01103

OAAI

Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome (vol 101, pg 239, 2017)

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2018-04-0113

OAAI

Lake, Nicole J.; Webb, Bryn D.; Stroud, David A.; Richman, Tara R.; Ruzzenente, Benedetta; Compton, Alison G.; Mountford, Hayley S.; Pulman, Juliette; Zangarelli, Coralie; Rio, Marlene; Boddaert, Nathalie; Assouline, Zahra; Sherpa, Mingma D.; Schadt, Eric E.; Houten, Sander M.; Byrnes, James; McCormick, Elizabeth M.; Zolkipli-Cunningham, Zarazuela; Haude, Katrina; Zhang, Zhancheng; Retterer, Kyle; Bai, Renkui; Calvo, Sarah E.; Mootha, Vamsi K.; Christodoulou, John; Rotig, Agnes; Filipovska, Aleksandra; Cristian, Ingrid; Falk, Marni J.; Metodiev, Metodi D.; Thorburn, David R.

Biallelic C1QBP Mutations Cause Severe Neonatal-, Childhood-, or Later-Onset Cardiomyopathy Associated with Combined Respiratory-Chain Deficiencies

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2017-10-0158

OAAI

Feichtinger, Rene G.; Olahova, Monika; Kishita, Yoshihito; Garone, Caterina; Kremer, Laura S.; Yagi, Mikako; Uchiumi, Takeshi; Jourdain, Alexis A.; Thompson, Kyle; D'Souza, Aaron R.; Kopajtich, Robert; Alston, Charlotte L.; Koch, Johannes; Sperl, Wolfgang; Mastantuono, Elisa; Strom, Tim M.; Wortmann, Saskia B.; Meitinger, Thomas; Pierre, Germaine; Chinnery, Patrick F.; Chrzanowska-Lightowlers, Zofia M.; Lightowlers, Robert N.; DiMauro, Salvatore; Calvo, Sarah E.; Mootha, Vamsi K.; Moggio, Maurizio; Sciacco, Monica; Comi, Giacomo P.; Ronchi, Dario; Murayama, Kei; Ohtake, Akira; Rebelo-Guiomar, Pedro; Kohda, Masakazu; Kang, Dongchon; Mayr, Johannes A.; Taylor, Robert W.; Okazaki, Yasushi; Minczuk, Michal; Prokisch, Holger

Defective mitochondrial rRNA methyltransferase MRM2 causes MELAS-like clinical syndrome

HUMAN MOLECULAR GENETICS

IF3.2

2017-08-2559

OAAI

Biallelic Mutations in MRPS34 Lead to Instability of the Small Mitoribosomal Subunit and Leigh Syndrome

AMERICAN JOURNAL OF HUMAN GENETICS

IF8.1

2017-08-0177

OAAI

Lake, Nicole J.; Webb, Bryn D.; Stroud, David A.; Richman, Tara R.; Ruzzenente, Benedetta; Compton, Alison G.; Mountford, Hayley S.; Pulman, Juliette; Zangarelli, Coralie; Rio, Marlene; Bodaert, Nathalie; Assouline, Zahra; Sherpa, Mingma D.; Schadt, Eric E.; Houten, Sander M.; Byrnes, James; McCormick, Elizabeth M.; Zolkipli-Cunningham, Zarazuela; Haude, Katrina; Zhang, Zhancheng; Retterer, Kyle; Bai, Renkui; Calvo, Sarah E.; Mootha, Vamsi K.; Christodoulou, John; Rotig, Agnes; Filipovska, Aleksandra; Cristian, Ingrid; Falk, Marni J.; Metodiev, Metodi D.; Thorburn, David R.

Comparative Analysis of Mitochondrial N-Termini from Mouse, Human, and Yeast

小鼠，人类和酵母线粒体N末端的比较分析

MOLECULAR & CELLULAR PROTEOMICS

IF5.5

2017-04-0172

OAAI

Sarah E. Calvo

个人简介

教育背景

工作经历

荣誉奖项

研究方向