Research Grant Program
2025 Request for Research Proposals (Now Open)
Since 2002, the Barth Syndrome Foundation, Inc. and its affiliates have been awarding research grants. The Barth Syndrome Foundation of Canada have participated in their Research Grant program since 2006, and have contributed towards 19 individual grants for a total of over $450,000 US (see below for details).
The 2025 grant cycle is now open. The Barth Syndrome Foundation (BSF) and its international affiliates will welcome innovative applications that address the basic, translational, and clinical research challenges of Barth syndrome. BSF will seeks to provide seed grant funding to young and established investigators in order to generate the preliminary data required for successful follow-on funding available from major grant-making institutions.
More information about the program and key dates can be found at BSF.
2024 Grant Awarded
David Stokes, PhD,
New York University
Mechanism of cardiolipin remodeling by TAFAZZIN
This research is currently on-going.
*Funding for this award was provided by Barth Syndrome Foundation, Barth Syndrome Foundation of Canada, and Barth Italia.
Previous Grants Awarded
Note that BSF has adjusted their grant year naming convention, so 2019 was not considered a grant year.
Click here for a complete list of active grants awarded by BSF and affiliates. Following is a list of grants funded or partially funded by BSFCa.
2023
Kate Schroder, PhD,
The University of Queensland, Australia
Elucidating Cardiolipin Immune Dysfunction in Barth Syndrome
This research is currently on-going.
*Funding for this award was provided by Barth Syndrome Foundation and Barth Syndrome Foundation of Canada.
2022
Borko Amulic, PhD
University of Bristol, Bristol, UK
Investigating the basis of neutropenia in Barth syndrome
This research is currently on-going.
*Funding for this award was provided by Barth Syndrome UK, and Barth Syndrome Foundation of Canada.
2021
Jason Moffat, PhD
Professor, University of Toronto, Toronto, ON, Canada
Surveying TAZ genetic interactions and mutational landscape in human cells. This research is currently on-going.
*Funding for this award was provided by Barth Syndrome UK, and Barth Syndrome Foundation of Canada.
2020
Robin E. Duncan, PhD
Associate Professor, University of Waterloo, Waterloo, ON, Canada
Investigation of a new nutraceutical for treatment of Barth Syndrome. This research is currently on-going.
*Funding for this award was provided by Barth Syndrome UK, and Barth Syndrome Foundation of Canada.
2018
Christopher Y. Park, MD, PhD
Associate Professor, New York University School of Medicine, New York, NY
Characterization of hematopoietic stem and progenitor cells in Barth syndrome. This research is currently on-going.
*Funding for this award was provided by Barth Syndrome France, and Barth Syndrome Foundation of Canada.
2017
Richard Epand, PhD
Professor, McMaster University, Hamilton, Ontario, Canada
The cause and consequences of plasmalogen depletion in Barth syndrome. This research is currently on-going.
Associated publications to date:
- Kimura T, Kimura AK, Ren M, Monteiro V, Xu Y, Berno B, Schlame M, Epand RM. Plasmalogen loss caused by remodeling deficiency in mitochondria. Life Sci Alliance. 2019 Aug 21;2(4). pii: e201900348. doi:10.26508/lsa.201900348. Print 2019 Aug. (PubMed – Open Access)*
*Funding for this award was provided by the Barth Syndrome Foundation, and the Barth Syndrome Foundation of Canada.
2016
Christina Pacak, PhD
Assistant Professor, University of Florida, Gainesville, FL
Optimization of AAV-mediated gene therapy for Barth syndrome. This research is currently on-going.
Associated publications to date:
- Suzuki-Hatano S, Sriramvenugopal M, Ramanathan M, Soustek M, Byrne BJ, Cade WT, Kang PB, Pacak CA. Increased mtDNA abundance and improved function in human Barth syndrome patient fibroblasts following AAV-TAZ gene delivery. Int J Mol Sci. 2019 Jul 11;20(14). Pii: e3416. Doi: 10.3390/ijms20143416. (PubMed – Open Access) *▼
- Suzuki-Hatano S, Saha M, Rizzo SA, Witko RL, Gosiker BJ, Ramanathan M, Soustek MS, Jones MD, Kang PB, Byrne BJ, Cade WT, Pacak CA. AAV-mediated TAZ gene replacement restores mitochondrial and cardioskeletal function in Barth syndrome. Hum Gene Ther. 2019 Feb;30(2):139-154. doi: 10.1089/hum.2018.020. Epub 2018 Oct 3. (PubMed Abstract)*
- Suzuki-Hatano S, Saha M, Soustek MS, Kang PB, Byrne, BJ, Cade WT, Pacak CA. AAV9-TAZ gene replacement ameliorates cardiac TMT proteomic profiles in a mouse model of Barth syndrome. Mol Ther Methods Clin Dev. 2019 Jan 25;13:167-179. doi: 10.1016/j.omtm.2019.01.007. eCollection 2019 Jun 14. (Open Access)*
*Funding for this award was provided by Barth Syndrome France, and Barth Syndrome Foundation of Canada.
2015
Robin Duncan
Assistant Professor, University of Waterloo, Waterloo, Ontario
A new enzyme and pathway in cardiolipin synthesis. This research is currently on-going
*Funding for this award was provided by Barth Syndrome France, and Barth Syndrome Foundation of Canada.
2014
Valerian Kagan, PhD
Professor and Vice-Chairman, University of Pittsburgh, Pittsburgh, PA
Mechanism and role of cardiolipin oxidation and hydrolysis in Barth syndrome. Associated publications to date:
- Chao H, Anthonymuthu TS, Kenny EM, Amoscato AA, Cole LK, Hatch GM, Ji J, Kagan VE, Bayır H. Disentangling oxidation/hydrolysis reactions of brain mitochondrial cardiolipins in pathogenesis of traumatic injury. JCI Insight. 2018 Nov 2;3(21). pii: 97677. doi: 10.1172/jci.insight.97677. [Epub ahead of print] (PubMed – Open Access)*
- Cole LK, Kim JH, Amoscato AA, Tyurina YY, Bayir H, Karimi B, Siddiqui TJ, Kagan VE, Hatch GM, Kauppinen TM. Aberrant cardiolipin metabolism is associated with cognitive deficiency and hippocampal alteration in tafazzin knockdown mice. Biochim Biophys Acta. 2018 Jul 25. pii: S0925-4439(18)30271-0. doi: 10.1016/j.bbadis.2018.07.022. [Epub ahead of print] (PubMed Abstract)*
- Kagan VE, Bayir H, Tyurina YY, Bolevich SB, Maguire JJ, Fadeel B, Balasubramanian K. Elimination of the unnecessary: Intra- and extracellular signaling by anionic phospholipids. Review Article. Biochemical and Biophysical Research Communications, Volume 482, issue 3, 15 January 2017, Pages 482-490. (PubMed Abstract)*
- Tyurina YY, Lou W, Qu F, Tyurin VA, Mohammadyani D, Liu J, Hüttemann M, Frasso MA, Wipf P, Bayir H, Greenberg ML, Kagan VE. Lipidomics characterization of biosynthetic and remodeling pathways of cardiolipins in genetically and nutritionally manipulated yeast cells. ACS Chem Biol. 2016 Dec 16. [Epub ahead of print] (PubMed Abstract)*
- Kooijman EE, Swim LA, Graber ZT, Tyurina YY, Bayir H, Kagan VE. Magic angle spinning 31P NMR spectroscopy reveals two essentially identical ionization states for the cardiolipin phosphates in phospholipid liposomes. Biochim Biophys Acta. 2016 Oct 26. pii: S0005-2736(16)30346-7. doi:10.1016/j.bbamem.2016.10.013. [Epub ahead of print] (PubMed Abstract)*
- Maguire JJ, Tyurina YY, Mohammadyani D, Kapralov AA, Anthonymuthu TS, Qu F, Amoscato AA, Sparvero LJ, Tyurin VA, Planas-Iglesias J, He RR, Klein-Seetharaman J, Bayir H, Kagan VE. Known unknowns of cardiolipin signaling: The best is yet to come. Biochim Biophys Acta. 2016 Aug 4. pii: S1388-1981(16)30221-9. doi: 10.1016/j.bbalip.2016.08.001. [Epub ahead of print] (PubMed Abstract)*
Associated presentations to date:
- Multitasking by cardiolipins – intra- and extra-mitochondrial events (BSF 2016 Conference – July 22, 2016)
- Rancid radical talk: Music of mitochondrial cardiolipins (BSF 2014 Conference – June 26, 2014)
*Funding for this award was provided by Barth Syndrome France, and Barth Syndrome Foundation of Canada.
2013
Grant Hatch, PhD
Professor, University of Manitoba, Winnipeg, Manitoba
Tafazzin knockdown alters hepatic lipid metabolism. Associated publications to date:
- Mejia EM, Zinko JC, Hauff KD, Xu Fy, Ravandi A, Hatch GM. Glucose uptake and triacylglycerol synthesis are increased in Barth syndrome lymphoblasts. Lipids. 2017 Jan 17. doi: 10.1007/s11745-017-4232-7. [Epub ahead of print] (PubMed Abstract)*
*Funding for this award was provided by Barth Syndrome France, and Barth Syndrome Foundation of Canada.
2012
Richard Epand, PhD
Professor, McMaster University, Hamilton, Ontario
Relationship between membrane physical properties and the action of tafazzin. Associated Publications to Date:
- Xu Y, Phoon CK, Berno B, D’Souza K, Hoedt E, Zhang G, Neubert TA, Epand RM, Ren M, Schlame M. Loss of protein association causes cardiolipin degradation in Barth syndrome. Nat Chem Biol. 2016 Jun 27. doi: 10.1038/nchembio.2113. [Epub ahead of print] (PubMed Abstract)
*Funding for this award was provided by the Barth Syndrome Foundation, and the Barth Syndrome Foundation of Canada.
2011
Grant Hatch, PhD
Professor, University of Manitoba, Winnipeg, Manitoba
MLCL AT-1 elevates cardiolipin and mitochondrial function in cardiac myocytes of taz knockdown mice.
Associated Publications To Date:
- Mejia EM, Nguyen H, Hatch GM. Mammalian cardiolipin biosynthesis. Chem Phys Lipids. 2013 Oct 18 [Epub ahead of print](PubMed Abstract)
Associated Presentations To Date:
2010
Christopher McMaster, PhD
Professor, Dalhousie University, Halifax, Nova Scotia
A screen for drugs, leads for the treatment of Barth syndrome.
Associated Publications to Date:
- Gaspard GJ, McMaster CR. Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome. Chem Phys Lipids. 2015 Sep 25. pii: S0009-3084(15)30054-2. doi:10.1016/j.chemphyslip.2018.09.005.[Epub ahead of print] Review. (PubMed Abstract)*
- Gaspard GJ, McMaster CR. The mitochondrial quality control protein Yme1 is necessary to prevent defective mitophagy in a yeast model of Barth syndrome. J Biol Chem. 2015 Feb 16. pii:jbc.M115.41878.[Epub ahead of print] (PubMed – Open Access)*
Associated Presentations To Date:
- Yeast genome-wide screens to assess the genetic landscape for Barth syndrome (PDF Presentation) (Video File)
2009
Grant Hatch, PhD
Professor, University of Manitoba, Winnipeg, Manitoba
Role of human monolysocardiolipin acyltransferase in Barth syndrome.
Associated Publications To Date:
- Taylor WA, Mejia EM, Mitchell RW, Choy PC, Sparagna GC, et al. Human trifunctional protein alpha links cardiolipin remodeling to beta-oxidation. PLoS ONE 7(11): e48628.(PubMed ~ OpenAccess)
- Saini-Chohan HK, Mitchell RW, Vaz FM, Zelinski T, Hatch GM. Delineating the role of alterations in lipid metabolism to the pathogenesis of inherited skeletal and cardiac muscle disorders. J Lipid Res. 2012 Jan;53(1):4-27. doi: 10.1194/jlr.R012120. Epub 2011 Nov 7.(PubMed ~ OpenAccess)
- Saini-Chohan HK, Dakshinamurti S, Taylor WA, Shen GX, Murphy R, Sparagna GC, Hatch GM. Persistent pulmonary hypertension results in reduced tetralinoleoyl-cardiolipin and Complex II + III activity in neonatal pig heart. Am J Physiol Heart Circ Physiol. 2011 Oct;301(4):H1415-24. doi: 10.1152/ajpheart.00247.2011. Epub 2011 Aug 12.(PubMed ~ OpenAccess)
2008
Miriam Greenberg, PhD
Professor and Associate Dean, Wayne State University, Detroit, Michigan
The role of tafazzin in mitochondrial protein import – Implications for Barth syndrome
Associated Publications To Date:
- Tyurina YY, Lou W, Qu F, tyurin VA, Mohammadyani D, Liu J, Hüttemann M, Frasso MA, Wipf P, Bayer H, Greenberg ML, Kagan VE. Lipidomics characterization of biosynthetic and remodeling pathways of cardiolipins in genetically and nutritionally manipulated yeast cells. ACS Chem Biol. 2016 Dec 16. [Epub ahead of print] (PubMed – OpenAccess)*
- Raja V, Joshi AS, Li G, Maddipati KR, Greenberg ML. Loss of cardiolipin leads to perturbation of acetyl-CoA synthesis. J Biol Chem. 2016 Dec 9. pii: jbc.M116.753624. [Epub ahead of print] (PubMed Abstract)*
- Chen S, Liu D, Finley RL Jr, Greenberg ML. Loss of mitochondrial DNA in the yeast cardiolipin synthase crd1 mutant leads to up-regulation of the protein kinase Swe1p that regulates the G2/M transition. J Biol Chem. 2010 Apr 2;285(14):10397-407. doi: 10.1074/jbc.M110.100784. Epub 2010 Jan 19. (PubMed ~ OpenAccess)
- Gebert N, Joshi AS, Kutik S, Becker T, McKenzie M, Guan XL, Mooga VP, Stroud DA, Kulkarni G, Wenk MR, Rehling P, Meisinger C, Ryan MT, Wiedemann N, Greenberg ML, Pfanner N. Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome. Curr Biol. 2009 Dec 29;19(24):2133-9. Epub 2009 Dec 3. (PubMed Abstract)
*Funding for this award was provided by the Barth Syndrome Foundation, and the Barth Syndrome Foundation of Canada.
2007
Richard Epand, PhD
Professor, McMaster University, Hamilton, Ontario
Consequences of the alteration of cardiolipin structure on the properties of the mitochondrial membranes.
Associated Publications To Date:
- Schlame M, Acehan D, Berno B, Xu Y, Valvo S, Ren M, Stokes DL, Epand RM. The physical state of lipid substrates provides transacylation specificity for tafazzin. Nat Chem Biol. 2012 Oct;8(10):862-9.(PubMed Abstract)
- Schlattner U, Tokarska-Schlattner M, Ramirez S, Brückner A, Kay L, Polge C, Epand RF, Lee RM, Lacombe ML, Epand RM. Mitochondrial kinases and their molecular interaction with cardiolipin. Biochim Biophys Acta. 2009 Oct;1788(10):2032-47. Epub 2009 May 4. Review. (PubMed Abstract)
Associated Presentations To Date:
- U.Schlattner, M.Tokarska-Schlattner, S.Ramirez, A.Bruckner, L.Kay, C.Polge, R.F.Epand, R.M.Lee, M.L.Lacombe, and R.M.Epand, Mitochondrial kinases and their molecular interaction with cardiolipin. Biochim Biophys Acta 1788 (2009) 2032-2047.
- T. H. Haines, R. F. Epand and R. M. Epand. The pK´s of cardiolipins are altered by the number and position of their specific fatty acid esters. Biophysical Society – 52th Annual Meeting, Long Beach, CA (February, 2008).
2007
Christopher R. McMaster, PhD
Assistant Professor, Dalhousie University, Halifax, Nova Scotia
Synthetic genetics toward understanding Barth syndrome cell biology
Associated Publications to Date:
- Gaspard GJ, McMaster CR. Cardiolipin metabolism and its causal role in the etiology of the inherited cardiomyopathy Barth syndrome. Chem Phys Lipids. 2015 Sep 25. pii: S0009-3084(15)30054-2. doi:10.1016/j.chemphyslip.2018.09.005.[Epub ahead of print] Review. (PubMed Abstract)*
- Gaspard GJ, McMaster CR. The mitochondrial quality control protein Yme1 is necessary to prevent defective mitophagy in a yeast model of Barth syndrome. J Biol Chem. 2015 Feb 16. pii:jbc.M115.41878.[Epub ahead of print] (PubMed – Open Access)*
*Funding for this award was provided by the Barth Syndrome Foundation, and the Barth Syndrome Foundation of Canada.
2006
Grant M. Hatch, PhD
Professor, Pharmacology and Therapeutics, Acting Associate Dean of Medicine for Research
University of Manitoba, Winnipeg, Manitoba
Cholesterol Metabolism in Barth syndrome
Associated Publications To Date:
- Hauff K, Hatch GM. Reduction in cholesterol synthesis in response to serum starvation in lymphoblasts of a patient with Barth syndrome. Biochem Cell Biol. 2010 Aug;88(4):595-602. (PubMed Abstract)
- Hauff KD, Choi SY, Frohman MA, Hatch GM. Cardiolipin synthesis is required to support human cholesterol biosynthesis from palmitate upon serum removal in Hela cells. Can J Physiol Pharmacol. 2009 Oct;87(10):813-20. (PubMed Abstract)
- Hauff KD, Hatch, GM. Cardiolipin metabolism and Barth Syndrome. Prog Lipid Res. 2006 Mar;45(2):91-101. Epub 2006 Jan 18. (PubMed Abstract)