Maffucci Syndrome, Calcium Homeostasis, and Endocrine Challenges in Management

od Ginnard, Olivia Z B, Burrage, Lindsay C, Karaviti, Lefkothea P
izdano v J Endocr Soc (2021)

19-Year Follow-up of A Patient With Severe Glutathione Synthetase Deficiency

od Atwal, Paldeep S., Medina, Casey R., Burrage, Lindsay C., Sutton, V. Reid
izdano v J Hum Genet (2016)

Branched-chain amino acid metabolism: from rare Mendelian diseases to more common disorders

od Burrage, Lindsay C., Nagamani, Sandesh C.S., Campeau, Philippe M., Lee, Brendan H.
Izdano 2014

Catel–Manzke syndrome: Further delineation of the phenotype associated with pathogenic variants in TGDS

od Pferdehirt, Rachel, Jain, Mahim, Blazo, Maria A., Lee, Brendan, Burrage, Lindsay C.
izdano v Mol Genet Metab Rep (2015)

Sodium Phenylbutyrate Decreases Plasma Branched-Chain Amino Acids in Patients with Urea Cycle Disorders

od Burrage, Lindsay C., Jain, Mahim, Gandolfo, Laura, Lee, Brendan H., Nagamani, Sandesh CS.
Izdano 2014

Pleiotropy, Homeostasis, and Functional Networks Based on Assays of Cardiovascular Traits in Genetically Randomized Populations

od Nadeau, Joseph H., Burrage, Lindsay C., Restivo, Joe, Pao, Yoh-Han, Churchill, Gary, Hoit, Brian D.
Izdano 2003

A Mosaic 2q24.2 Deletion Narrows the Critical Region to a 0.4 Mb Interval That Includes TBR1, TANK, and PSMD14

od Burrage, Lindsay C., Eble, Tanya N., Hixson, Patricia M., Roney, Erin K., Cheung, Sau W., Franco, Luis M.
izdano v Am J Med Genet A (2013)

A deep intronic variant is a common cause of OTC deficiency in individuals with previously negative genetic testing

od Kumar, Runjun D., Burrage, Lindsay C., Bartos, Jan, Ali, Saima, Schmitt, Eric, Nagamani, Sandesh C.S., LeMons, Cynthia
izdano v Mol Genet Metab Rep (2021)

Increased mitochondrial oxidative phosphorylation in the liver is associated with obesity and insulin resistance

od Buchner, David A., Yazbek, Soha N., Solinas, Paola, Burrage, Lindsay C., Morgan, Michael G., Hoppel, Charles L., Nadeau, Joseph H.
Izdano 2010

Biomarkers for Liver Disease in Urea Cycle Disorders

od Nagamani, Sandesh C.S., Ali, Saima, Izem, Rima, Schady, Deborah, Masand, Prakash, Shneider, Benjamin L., Leung, Daniel H., Burrage, Lindsay C.
izdano v Mol Genet Metab (2021)

Resistance to diet-induced obesity in mice with a single substituted chromosome

od Buchner, David A., Burrage, Lindsay C., Hill, Annie E., Yazbek, Soha N., O'Brien, William E., Croniger, Colleen M., Nadeau, Joseph H.
Izdano 2008

Milder Clinical and Biochemical Phenotypes Associated with the c.482G>A (p.Arg161Gln) Pathogenic Variant in Cobalamin C Disease: Implications for Management and Screening

od Almannai, Mohammed, Marom, Ronit, Divin, Kristian, Scaglia, Fernando, Sutton, V. Reid, Craigen, William J., Lee, Brendan, Burrage, Lindsay C., Graham, Brett H.
izdano v Mol Genet Metab (2017)

Maternal Folate Polymorphisms and the Etiology of Human Nondisjunction

od Hassold, Terry J., Burrage, Lindsay C., Chan, Ernest R., Judis, LuAnn M., Schwartz, Stuart, James, S. Jill, Jacobs, Patricia A., Thomas, N. Simon
Izdano 2001

Elevations of C14:1 and C14:2 Plasma Acylcarnitines in Fasted Children: A Diagnostic Dilemma

od Burrage, Lindsay C., Miller, Marcus J., Wong, Lee-Jun, Kennedy, Adam D., Sutton, V. Reid, Sun, Qin, Elsea, Sarah H., Graham, Brett H.
izdano v J Pediatr (2015)

Early Childhood Presentation of Czech Dysplasia

od Burrage, Lindsay C., Lu, James T., Liu, David S., Moss, Timothy J., Gibbs, Richard, Schlesinger, Alan E., Bacino, Carlos A., Campeau, Philippe M., Lee, Brendan H.
Izdano 2013

Analyzing complex traits with congenic strains

od Shao, Haifeng, Sinasac, David S., Burrage, Lindsay C., Hodges, Craig A., Supelak, Pamela J., Palmert, Mark R., Moreno, Carol, Cowley, Allen W., Jacob, Howard J., Nadeau, Joseph H.
Izdano 2010

Neonatal Fractures as a Presenting Feature of LMOD3-Associated Congenital Myopathy

od Abbott, Megan, Jain, Mahim, Pferdehirt, Rachel, Chen, Yuqing, Tran, Alyssa, Duz, Mehmet Bugrahan, Seven, Mehmet, Gibbs, Richard A., Muzny, Donna, Lee, Brendan, Marom, Ronit, Burrage, Lindsay C.
izdano v Am J Med Genet A (2017)

Pathogenic Variants in Fucokinase Cause a Congenital Disorder of Glycosylation

od Ng, Bobby G., Rosenfeld, Jill A., Emrick, Lisa, Jain, Mahim, Burrage, Lindsay C., Lee, Brendan, Craigen, William J., Bearden, David R., Graham, Brett H., Freeze, Hudson H.
izdano v Am J Hum Genet (2018)

Adult Presentation of X-Linked Conradi-Hünermann-Happle Syndrome

od Posey, Jennifer E., Burrage, Lindsay C., Campeau, Philippe M., Lu, James T., Eble, Tanya N., Kratz, Lisa, Schlesinger, Alan E., Gibbs, Richard A., Lee, Brendan H., Nagamani, Sandesh CS.
izdano v Am J Med Genet A (2015)

Deep congenic analysis identifies many strong, context-dependent QTLs, one of which, Slc35b4, regulates obesity and glucose homeostasis

od Yazbek, Soha N., Buchner, David A., Geisinger, Jonathan M., Burrage, Lindsay C., Spiezio, Sabrina H., Zentner, Gabriel E., Hsieh, Chang-Wen, Scacheri, Peter C., Croniger, Colleen M., Nadeau, Joseph H.
Izdano 2011