| scholarly article | Q13442814 |
| P50 | author | Kati Hyvärinen | Q52620845 |
| Satu Koskela | Q58879602 | ||
| Tony Kwan | Q88220821 | ||
| Jarmo Ritari | Q42118205 | ||
| Jukka Partanen | Q42707962 | ||
| P2093 | author name string | Tomi Pastinen | |
| Riitta Niittyvuopio | |||
| Maija Itälä-Remes | |||
| P2860 | cites work | PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 |
| A haplotype map of the human genome | Q24679827 | ||
| The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data | Q27860742 | ||
| Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex | Q28190352 | ||
| A framework for variation discovery and genotyping using next-generation DNA sequencing data | Q29547262 | ||
| Effective filtering strategies to improve data quality from population-based whole exome sequencing studies. | Q30828110 | ||
| From FastQ data to high confidence variant calls: the Genome Analysis Toolkit best practices pipeline | Q30872351 | ||
| Donor-recipient mismatch for common gene deletion polymorphisms in graft-versus-host disease | Q33583414 | ||
| Genomics of the major histocompatibility complex: haplotypes, duplication, retroviruses and disease | Q33630704 | ||
| A genome-wide study of Hardy-Weinberg equilibrium with next generation sequence data | Q33676593 | ||
| Data quality control in genetic case-control association studies. | Q33749328 | ||
| An integrated haplotype map of the human major histocompatibility complex | Q33906339 | ||
| A high-resolution linkage-disequilibrium map of the human major histocompatibility complex and first generation of tag single-nucleotide polymorphisms | Q33942154 | ||
| MHC-resident variation affects risks after unrelated donor hematopoietic cell transplantation | Q34290624 | ||
| Major histocompatibility complex genomics and human disease | Q34359146 | ||
| Multi-population classical HLA type imputation | Q34607788 | ||
| Inheritable variable sizes of DNA stretches in the human MHC: conserved extended haplotypes and their fragments or blocks | Q35177452 | ||
| Mismatched HLA-DRB3 Can Induce a Potent Immune Response After HLA 10/10 Matched Stem Cell Transplantation. | Q51115413 | ||
| Graft rejection after unrelated donor hematopoietic stem cell transplantation for thalassemia is associated with nonpermissive HLA-DPB1 disparity in host-versus-graft direction. | Q51959143 | ||
| Effect of major histocompatibility complex haplotype matching by C4 and MICA genotyping on acute graft versus host disease in unrelated hematopoietic stem cell transplantation. | Q52900700 | ||
| Single nucleotide polymorphisms and outcome risk in unrelated mismatched hematopoietic stem cell transplantation: an exploration study. | Q53168839 | ||
| The discovery of linkage between the MHC and genetic control of the immune response. | Q53420953 | ||
| Cutadapt removes adapter sequences from high-throughput sequencing reads | Q55953584 | ||
| Ancestral haplotypes: conserved population MHC haplotypes | Q67602836 | ||
| The major histocompatability complex (MHC) contains conserved polymorphic genomic sequences that are shuffled by recombination to form ethnic-specific haplotypes | Q73485677 | ||
| A simplified method for screening siblings for HLA identity using short tandem repeat (STR) polymorphisms | Q85842490 | ||
| Congruence as a measurement of extended haplotype structure across the genome. | Q35847732 | ||
| Association of HLA-G low expressor genotype with severe acute graft-versus-host disease after sibling bone marrow transplantation | Q35928084 | ||
| High HLA-DP Expression and Graft-versus-Host Disease | Q36028056 | ||
| Immunoseq: the identification of functionally relevant variants through targeted capture and sequencing of active regulatory regions in human immune cells | Q36131690 | ||
| The MICA-129 dimorphism affects NKG2D signaling and outcome of hematopoietic stem cell transplantation | Q36278732 | ||
| Intrahaplotypic Variants Differentiate Complex Linkage Disequilibrium within Human MHC Haplotypes | Q36305461 | ||
| Mapping MHC haplotype effects in unrelated donor hematopoietic cell transplantation | Q36666821 | ||
| Donor-recipient mismatches in MHC class I chain-related gene A in unrelated donor transplantation lead to increased incidence of acute graft-versus-host disease | Q36667913 | ||
| Population-specific recombination sites within the human MHC region | Q37026918 | ||
| Genetic similarity of chromosome 6 between patients receiving hematopoietic stem cell transplantation and HLA matched sibling donors | Q37146048 | ||
| High-resolution patterns of meiotic recombination across the human major histocompatibility complex | Q37202950 | ||
| Novel HLA-DP region susceptibility loci associated with severe acute GvHD. | Q37559942 | ||
| SEQMINER: An R-Package to Facilitate the Functional Interpretation of Sequence-Based Associations | Q38386637 | ||
| HLA mismatching as a strategy to reduce relapse after alternative donor transplantation | Q38783831 | ||
| Multi-SNP analysis of MHC region: remarkable conservation of HLA-A1-B8-DR3 haplotype | Q40330077 | ||
| A single high-resolution HLA mismatch has a similar adverse impact on the outcome of related hematopoietic stem cell transplantation as a single low-resolution HLA mismatch | Q41104915 | ||
| A T-cell epitope encoded by a subset of HLA-DPB1 alleles determines nonpermissive mismatches for hematologic stem cell transplantation | Q42611632 | ||
| Nonpermissive HLA-DPB1 disparity is a significant independent risk factor for mortality after unrelated hematopoietic stem cell transplantation | Q45172988 | ||
| Genetic polymorphism related to monocyte-macrophage function is associated with graft-versus-host disease. | Q45853292 | ||
| A linkage disequilibrium map of the MHC region based on the analysis of 14 loci haplotypes in 50 French families | Q47681972 | ||
| HLA-DPB1 mismatch induces a graft-versus-leukemia effect without severe acute GVHD after single-unit umbilical cord blood transplantation | Q50204017 | ||
| Matching for the MICA-129 polymorphism is beneficial in unrelated hematopoietic stem cell transplantation | Q50224813 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | sibling | Q31184 |
| P304 | page(s) | 5396 | |
| P577 | publication date | 2018-03-29 | |
| P1433 | published in | Scientific Reports | Q2261792 |
| P1476 | title | Hidden genomic MHC disparity between HLA-matched sibling pairs in hematopoietic stem cell transplantation | |
| P478 | volume | 8 |
| Q92404871 | Computational Analysis of HLA-presentation of Non-synonymous Recipient Mismatches Indicates Effect on the Risk of Chronic Graft-vs.-Host Disease After Allogeneic HSCT | cites work | P2860 |
Search more.