PeterRussellBakerIIMDFAAP, FACMGG

PubMed

• 10 citations
  Leucine acutely potentiates glucose-stimulated insulin secretion in fetal sheep
  Brit H Boehmer, Peter R. Baker, Laura D. Brown, Stephanie R. Wesolowski, Paul J. Rozance
  The Journal of Endocrinology. 2020-10-01
• 160 citations
  Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5.
  Peter R. Baker, Marisa W. Friederich, Michael A. Swanson, Tamim H. Shaikh, Kaustuv Bhattacharya
  Brain. 2014-02-01
• 19 citations
  Skeletal muscle amino acid uptake is lower and alanine production is greater in late gestation intrauterine growth-restricted fetal sheep hindlimb
  Eileen I. Chang, Stephanie R. Wesolowski, Elizabeth A. Gilje, Peter R. Baker, Julie A. Reisz
  American Journal of Physiology. Regulatory, Integrative and Comparative Physiology. 2019-09-04

Journal Articles

• "The Past, Present, and Future of Genetic Association in Type 1 Diabetes"  
  Peter Baker and Andrea Steck, Curr Diab Rep, 1/1/2011
• "Type 1 Diabetes: Pathogenesis, Prediction, and Prevention"  
  P. Baker and G.S. Eisenbarth, US Endocrinology, 11/1/2009
• "Cerebrotendinous Xanthomatosis"  
  Peter Baker and Robert Steiner, E-medicine, 1/1/2008

Abstracts/Posters

• "Prader-Willi Syndrome: Microdeletion in Exons 2&3 of SNRPN with Preserved Expression of SNURF and HBII-85 snoRNA Cluster"
  Peter Baker, Dobromir Slavov, Cara Wells, Jean Jirikowic, Terry Boyle, Matthew Taylor., American College of Medical Genetics and Genomics, Phoenix, AZ, 3/19/2013
• "Spastic Diplegia In A Novel Form Of Non-Ketotic Hyperglcycinaemia Due To Glrx5 Deficiency"
  K Bhattacharya, G Scharer, S Gupta, P Procopis, D Gill, B Wilcken, G Creadon-Swindel, J Aicher, P Baker, T Shaikh, F Frerman, M Friederich, E Spector, M Woontner, J C..., Society for the Study of Inborn Errors in Metabolism, Birmingham, UK, 9/4/2012
• "Defects in Lipoic Acid Synthesis Cause "Variant" Non-ketotic Hyperglycinemia"
  Baker P, Scharer G, Creadon-Swindel G, Aicher J, Shaikh T, Frerman F, Friederich M, Spector E, Cameron J, Robinson B, Bhattacharya K, Thorburn D, Raiman J, Charu D, Le..., Society for Inherited Metabolic Disease Annual Meeting, Charlotte, NC, 3/30/2012
• "ATPase4A autoreactivity and its association with autoimmune phenotypes in the T1DGC study"
  Janet Wenzlau, Pamela R. Fain, Peter Baker, George Eisenbarth, and John Hutton, T1DGC Autoantibody Workshop, Bethesda, MD, 7/7/2011
• "Genetic control of autoimmune thyroiditis in type 1 diabetes: data from the T1DGC"
  Heinrich Kahles, Peter Baker, Pam Fain, George Eisenbarth, and Klaus Badenhoop, T1DGC Autoantibody Workshop, Bethesda, MD, 7/7/2011
• "Genetic Determinants of 21-hydroxylase Autoantibodies Amongst Patients of the T1DGC"
  Peter Baker, Pam Fain, Heinrich Kahles, Liping Yu, John Hutton, Janet Wenzlau, Marian Rewers, Klaus Badenhoop, and George Eisenbarth, T1DGC Autoantibody Workshop, Bethesda, Maryland, 6/7/2011
• "Genetic Susceptibility to Autoimmune Addison's Disease"
  Peter R. Baker, Erin E. Baschal, Pam R. Fain, Taylor M. Triolo, Priyaanka Nanduri, Janet C. Siebert, Taylor K. Armstrong, Kelly Johnson, Sunanda R. Babu, Marian J. Rew..., PSDP Annual Meeting, San Diego, CA, 3/4/2011
• "Early Identification of Rare Syndromic Forms of Diabetes Mellitus"
  Peter Baker, Andrea Steck, Kelly Johnson, Brian Bucca, Michelle Haarhues, Georgeanna Klingensmith, Marian Rewers, George Eisenbarth, NIH Rare Diseases Clinical Research Network. Bethesda, MD, 9/22/2010
• "ND3 Mutation 10191T>C Causes Rapidly Progressive Infantile Leigh Disease"
  P R Baker, M Friederich, C Rice, L-J Wong, and J LK Van Hove, 33rd Society for Inherited Metabolic Disease (SIMD) Annual Meeting. Albuquerque, NM, 3/1/2010
• "Comparative Haplotypic Congruence Analysis of Addison's Disease and Type 1A Diabetes"
  E.E. Baschal, P.R. Baker, J.C. Siebert, T.M. Triolo, P. Nanduri, T.K. Armstrong, J.M. Jasinski, K.N. Johnson, S.R. Babu, P.A. Gottlieb, P.R. Fain, J.M. Barker, M.J. Re..., American Society of Human Genetics (ASHG) Annual Meeting, 10/1/2009
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