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EMBO Molecular Medicine|June 16, 2021
Long-lived macrophage reprogramming drives spike protein-mediated inflammasome activation in COVID-19Sebastian J Theobald, Alexander Simonis, Theodoros Georgomanolis, et al.Nature Communications|February 22, 2018
Clonal dynamics towards the development of venetoclax resistance in chronic lymphocytic leukemiaCarmen D Herling, Nima Abedpour, Jonathan Weiss, et al.Human Mutation|June 6, 2006
Mutations in the lipoma HMGIC fusion partner-like 5 (LHFPL5) gene cause autosomal recessive nonsyndromic hearing lossErsan Kalay, Yun Li, Abdullah Uzumcu, et al.Human Mutation|October 15, 2013
Extreme growth failure is a common presentation of ligase IV deficiencyJennie E Murray, Louise S Bicknell, Gökhan Yigit, et al.Nature Genetics|December 7, 2010
CEP152 is a genome maintenance protein disrupted in Seckel syndromeErsan Kalay, Gökhan Yigit, Yakup Aslan, et al.European Journal of Human Genetics : EJHG|January 22, 2009
An evaluation of the genetic-matched pair study design using genome-wide SNP data from the European populationTimothy Tehua Lu, Oscar Lao, Michael Nothnagel, et al.Orphanet Journal of Rare Diseases|May 20, 2021
Identification of two novel bullous pemphigoid- associated alleles, HLA-DQA1*05:05 and -DRB1*07:01, in GermansChristian Schwarm, Damian Gola, Maike M Holtsche, et al.Nature Genetics|November 24, 2015
TRAIP promotes DNA damage response during genome replication and is mutated in primordial dwarfismMargaret E Harley, Olga Murina, Andrea Leitch, et al.Current Biology : CB|August 12, 2008
Correlation between genetic and geographic structure in EuropeOscar Lao, Timothy T Lu, Michael Nothnagel, et al.Scientific Reports|February 16, 2019
Whole Genome Sequence, Variant Discovery and Annotation in Mapuche-Huilliche Native South AmericansElena A Vidal, Tomás C Moyano, Bernabé I Bustos, et al.Pageof 52