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The Journal of Clinical Endocrinology and Metabolism|December 16, 2004
Childhood obesityPhyllis W Speiser, Mary C J Rudolf, Henry Anhalt, et al.
Cell Reports. Medicine|June 20, 2024
Intergenic risk variant rs56258221 skews the fate of naive CD4+ T cells via miR4464-BACH2 interplay in primary sclerosing cholangitisTobias Poch, Jonas Bahn, Christian Casar, et al.
Nature Genetics|April 8, 2009
A common variant on chromosome 11q13 is associated with atopic dermatitisJorge Esparza-Gordillo, Stephan Weidinger, Regina Fölster-Holst, et al.
Molecular Cell|February 22, 2023
Evolutionary origins and interactomes of human, young microproteins and small peptides translated from short open reading framesClara-L Sandmann, Jana F Schulz, Jorge Ruiz-Orera, et al.
Immunology|October 10, 2023
Secondary Streptococcus pneumoniae infection increases morbidity and mortality during murine cryptococcosisBárbara A Miranda, Gustavo J C Freitas, Victor A T Leocádio, et al.
American Journal of Human Genetics|June 18, 2013
Fine mapping of the 1p36 deletion syndrome identifies mutation of PRDM16 as a cause of cardiomyopathyAnne-Karin Arndt, Sebastian Schafer, Jorg-Detlef Drenckhahn, et al.
The Journal of Clinical Investigation|December 13, 2016
Deficiency in prohormone convertase PC1 impairs prohormone processing in Prader-Willi syndromeLisa C Burnett, Charles A LeDuc, Carlos R Sulsona, et al.
Plos One|June 26, 2026
Awareness, attitudes, and barriers toward Transthyretin Amyloid Cardiomyopathy in Latin America: A questionnaire-based cross-sectional studyCecilia Camacho-Hubner, Marcia Waddington-Cruz, María Juliana Rodríguez-González, et al.
Genome Research|May 1, 2010
The genome sequence of the spontaneously hypertensive rat: Analysis and functional significanceSantosh S Atanur, Inanç Birol, Victor Guryev, et al.
Nature Genetics|April 30, 2008
Integrated genomic approaches implicate osteoglycin (Ogn) in the regulation of left ventricular massEnrico Petretto, Rizwan Sarwar, Ian Grieve, et al.
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