<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hernandez-Fuentes MP</submitter><funding>Guy&amp;apos;s and St Thomas&amp;apos; Charity</funding><funding>Oxford University Hospitals NHS Trust</funding><funding>Medical Research Council</funding><funding>NHS Blood and Transplant</funding><funding>National Institute for Health Research (NIHR)</funding><funding>Public Health Agency</funding><funding>Wellcome Trust</funding><pagination>1370-1379</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6001640</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>18(6)</volume><pubmed_abstract>Improvements in immunosuppression have modified short-term survival of deceased-donor allografts, but not their rate of long-term failure. Mismatches between donor and recipient HLA play an important role in the acute and chronic allogeneic immune response against the graft. Perfect matching at clinically relevant HLA loci does not obviate the need for immunosuppression, suggesting that additional genetic variation plays a critical role in both short- and long-term graft outcomes. By combining patient data and samples from supranational cohorts across the United Kingdom and European Union, we performed the first large-scale genome-wide association study analyzing both donor and recipient DNA in 2094 complete renal transplant-pairs with replication in 5866 complete pairs. We studied decease</pubmed_abstract><journal>American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons</journal><pubmed_title>Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study.</pubmed_title><pmcid>PMC6001640</pmcid><funding_grant_id>STL/3714/07</funding_grant_id><funding_grant_id>NF-SI-0510-10142</funding_grant_id><funding_grant_id>MC_PC_15025</funding_grant_id><funding_grant_id>STL/4760/13</funding_grant_id><funding_grant_id>G0802068</funding_grant_id><funding_grant_id>MR/K002996/1</funding_grant_id><funding_grant_id>WT098051</funding_grant_id><funding_grant_id>090355/A/09/Z</funding_grant_id><funding_grant_id>MR/K500999/1</funding_grant_id><funding_grant_id>R080530</funding_grant_id><funding_grant_id>NF-SI-0512-10074</funding_grant_id><funding_grant_id>WT091310</funding_grant_id><funding_grant_id>G0801537/ID: 88245</funding_grant_id><funding_grant_id>G0701320</funding_grant_id><funding_grant_id>G0600698</funding_grant_id><funding_grant_id>090355/B/09/Z</funding_grant_id><funding_grant_id>G0600892</funding_grant_id><funding_grant_id>R090782</funding_grant_id><funding_grant_id>MR/J006742/1</funding_grant_id><funding_grant_id>088849/Z/09/Z</funding_grant_id><pubmed_authors>Sheerin N</pubmed_authors><pubmed_authors>Hammad A</pubmed_authors><pubmed_authors>Phelan P</pubmed_authors><pubmed_authors>Solomon E</pubmed_authors><pubmed_authors>Conlon P</pubmed_authors><pubmed_authors>Franklin C</pubmed_authors><pubmed_authors>Higgins R</pubmed_authors><pubmed_authors>Cavalleri G</pubmed_authors><pubmed_authors>Gagliano SA</pubmed_authors><pubmed_authors>Stephens H</pubmed_authors><pubmed_authors>MacPhee I</pubmed_authors><pubmed_authors>Newstead C</pubmed_authors><pubmed_authors>Weale ME</pubmed_authors><pubmed_authors>Powis S</pubmed_authors><pubmed_authors>Thuraisingham R</pubmed_authors><pubmed_authors>McKane W</pubmed_authors><pubmed_authors>Trembath R</pubmed_authors><pubmed_authors>Topham P</pubmed_authors><pubmed_authors>Opelz G</pubmed_authors><pubmed_authors>Fuggle S</pubmed_authors><pubmed_authors>Jardine A</pubmed_authors><pubmed_authors>Borrows R</pubmed_authors><pubmed_authors>Griffin S</pubmed_authors><pubmed_authors>Rowe P</pubmed_authors><pubmed_authors>United Kingdom and Ireland Renal Transplant Consortium (UKIRTC) and the Wellcome Trust Case Control Consortium (WTCCC)-3</pubmed_authors><pubmed_authors>Delaney F</pubmed_authors><pubmed_authors>Stapleton C</pubmed_authors><pubmed_authors>Soranzo N</pubmed_authors><pubmed_authors>Perucha E</pubmed_authors><pubmed_authors>Lord GM</pubmed_authors><pubmed_authors>Maxwell P</pubmed_authors><pubmed_authors>Rebollo-Mesa I</pubmed_authors><pubmed_authors>McLean A</pubmed_authors><pubmed_authors>Mollon J</pubmed_authors><pubmed_authors>Hernandez-Fuentes MP</pubmed_authors><pubmed_authors>Clarke B</pubmed_authors><pubmed_authors>Mark PB</pubmed_authors><pubmed_authors>Vaughan R</pubmed_authors><pubmed_authors>Leach T</pubmed_authors><pubmed_authors>Byrne C</pubmed_authors><pubmed_authors>Feehally J</pubmed_authors><pubmed_authors>Keogan M</pubmed_authors><pubmed_authors>Sacks SH</pubmed_authors><pubmed_authors>Clatworthy M</pubmed_authors><pubmed_authors>Marsh J</pubmed_authors><pubmed_authors>Augustine T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Long- and short-term outcomes in renal allografts with deceased donors: A large recipient and donor genome-wide association study.</name><description>Improvements in immunosuppression have modified short-term survival of deceased-donor allografts, but not their rate of long-term failure. Mismatches between donor and recipient HLA play an important role in the acute and chronic allogeneic immune response against the graft. Perfect matching at clinically relevant HLA loci does not obviate the need for immunosuppression, suggesting that additional genetic variation plays a critical role in both short- and long-term graft outcomes. By combining patient data and samples from supranational cohorts across the United Kingdom and European Union, we performed the first large-scale genome-wide association study analyzing both donor and recipient DNA in 2094 complete renal transplant-pairs with replication in 5866 complete pairs. We studied decease</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jun</publication><modification>2026-05-01T23:29:59.427Z</modification><creation>2025-05-29T21:18:26.265Z</creation></dates><accession>S-EPMC6001640</accession><cross_references><pubmed>29392897</pubmed><doi>10.1111/ajt.14594</doi></cross_references></HashMap>