Lindsay Burrage Lab

Publications

Master
Content

Stroup  BM, Marom R, Li X, Hsu C, Chang C, Truong LD, Dawson B, Grafe I, Chen Y, Jian  M, Lanza D, Green JR, Sun Q, Barrish JP, Ani S, Christiansen AE, Seavitt JR, Dickinson ME, Kheradmand F, Heaney JD, Lee B, Burrage LC. (2020).   A Global Slc7a7 Knockout Mouse Model Demonstrates Characteristic Phenotypes of Human Lysinuric Protein Intolerance.  Human Molecular Genetics.  29(13):2171-2184.  PMID: 32504080.

Burrage LC, Madan S, Li X, Ali S, Mohammad M, Stroup BM, Jiang M, Cela R, Bertin T,  Dai J, Guffey D, Finegold M, Members of the Urea Cycle Disorders Consortium, Nagamani  S, Minard CG, Marini J, Masand P, Schady D, Shneider BL, Leung DH, Bali D, Lee B.  (2020). Chronic Liver Disease and Impaired Hepatic Glycogen Metabolism in Argininosuccinate Lyase Deficiency. JCI Insight.  5(4):e132342. PMID: 31990680.

Pillai NR*, Stroup BM*, Poliner A, Rossetti L, Rawls B, Shayota BJ, Soler-Alfonso C, Tunuguntala HP, Goss J, Craigen W, Scaglia F, Sutton VR, Himes RW, Burrage LC.  (2019). Liver transplantation in propionic and methylmalonic acidemia: A single center study with literature review.  Mol Genet Metab. 128:431-443.  PMID: 31757659.  *co-first authors

Burrage LC, Thistlethwaite, L, Stroup BM, Sun, Q, Miller, MJ, Nagamani, SCS, Craigen W, Scaglia, F, Sutton VR, Graham B, Kennedy AD, Members of the UCDC,  Milosavljevic A, Lee BH,  Elsea SH.  (2019).  Untargeted Metabolomic Profiling Reveals Multiple Pathway Perturbations and New Clinical Biomarkers in Urea Cycle Disorders.   Genet Med.  21:1977-1986.  PMID: 30670878.

Burrage LC, Reynolds JJ, Baratang NV, Phillips JB, Wegner J, McFarquhar A, Higgs MR, Christiansen AE, Lanza DG, Seavitt JR, Jain M, Li X, Parry D, Raman V, Chitayat D, Chinn IK, Bertuch AA, Karaviti L, Schlesinger AE, Earl D, Bamshad M, Savarirayan R, Doddapaneni H, Muzny D, Jhangiani SN, Eng C, Gibbs RA, Bi W, Emrick L, Rosenfeld JA, Postlethwait J, Westerfield M, Dickinson ME, Beaudet AL, Ranza E, Huber C, Cormier-Daire V, Shen W, Mao R, Heaney JD, Orange JS, University of Washington Center for Mendelian Genomics, Undiagnosed Diseases Network, Bertola D, Yamamoto G, Baratela WAR, Butler M, Ali A, Adeli M, Cohn DH, Krakow D, Jackson AP, Lees M, Offiah AC, Carlston CM, Carey JC, Stewart GS, Bacino CA, Campeau PM, Lee B.  (2019). Biallelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes.  Am J Hum Genet. 104:422-438. PMID: 30773277.

For a full list of publications: https://www.ncbi.nlm.nih.gov/myncbi/lindsay.burrage.1/bibliography/public/