Pages that link to "Q47502873"
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The following pages link to Konrad J. Karczewski (Q47502873):
Displaying 50 items.
- Phased whole-genome genetic risk in a family quartet using a major allele reference sequence (Q21144940) (← links)
- Chapter 7: Pharmacogenomics (Q21563496) (← links)
- A new system for comparative functional genomics of Saccharomyces yeasts (Q24628747) (← links)
- Analysis of protein-coding genetic variation in 60,706 humans (Q26831376) (← links)
- Performance of genomic medicine (Q28658371) (← links)
- Ten Simple Rules to Enable Multi-site Collaborations through Data Sharing (Q28974676) (← links)
- Personal omics profiling reveals dynamic molecular and medical phenotypes (Q29614800) (← links)
- Annotation of functional variation in personal genomes using RegulomeDB (Q29614867) (← links)
- Mendelian randomization of blood lipids for coronary heart disease (Q30407506) (← links)
- STORMSeq: an open-source, user-friendly pipeline for processing personal genomics data in the cloud (Q30486640) (← links)
- Efficient genotype compression and analysis of large genetic-variation data sets. (Q31019979) (← links)
- Progress in genomics according to bingo: 2013 edition. (Q33745527) (← links)
- Performance comparison of exome DNA sequencing technologies (Q34023426) (← links)
- Health and population effects of rare gene knockouts in adult humans with related parents (Q34046351) (← links)
- Variation in transcription factor binding among humans (Q34105133) (← links)
- Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants (Q34146799) (← links)
- Genetic variant in folate homeostasis is associated with lower warfarin dose in African Americans. (Q34284362) (← links)
- Evidence that personal genome testing enhances student learning in a course on genomics and personalized medicine. (Q34918731) (← links)
- Coherent functional modules improve transcription factor target identification, cooperativity prediction, and disease association (Q35091271) (← links)
- Cooperative transcription factor associations discovered using regulatory variation (Q35164635) (← links)
- Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome (Q35958578) (← links)
- Genetic meta-analysis of 15,901 African Americans identifies variation in EXOC3L1 is associated with HDL concentration. (Q35994381) (← links)
- Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies (Q36110086) (← links)
- Extensive genetic variation in somatic human tissues (Q36397956) (← links)
- Quantifying prion disease penetrance using large population control cohorts (Q36639581) (← links)
- The origin, evolution, and functional impact of short insertion-deletion variants identified in 179 human genomes (Q36800421) (← links)
- Systematic functional regulatory assessment of disease-associated variants. (Q36915402) (← links)
- De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies (Q36959752) (← links)
- Population-specific single-nucleotide polymorphism confers increased risk of venous thromboembolism in African Americans (Q37257102) (← links)
- Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci (Q37634121) (← links)
- Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations (Q37705562) (← links)
- Regulatory variation within and between species. (Q37896646) (← links)
- Using ALoFT to determine the impact of putative loss-of-function variants in protein-coding genes (Q38603105) (← links)
- The future of genomic medicine is here. (Q39423257) (← links)
- Interpretome: a freely available, modular, and secure personal genome interpretation engine (Q39553107) (← links)
- Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity (Q40244307) (← links)
- Improving genetic diagnosis in Mendelian disease with transcriptome sequencing (Q42343467) (← links)
- Landscape of X chromosome inactivation across human tissues (Q42696435) (← links)
- Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. (Q55027605) (← links)
- Haplotype Sharing Provides Insights into Fine-Scale Population History and Disease in Finland (Q57255465) (← links)
- Human knockouts in a cohort with a high rate of consanguinity (Q57910670) (← links)
- Landscape of X chromosome inactivation across human tissues (Q57910760) (← links)
- Corrigendum: Landscape of X chromosome inactivation across human tissues (Q58928211) (← links)
- Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum (Q59566816) (← links)
- Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum (Q59566818) (← links)
- Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population (Q59566823) (← links)
- Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population (Q92404142) (← links)
- Bioinformatics challenges for personalized medicine (Q93579759) (← links)
- Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (Q95933674) (← links)
- Characterising the loss-of-function impact of 5' untranslated region variants in 15,708 individuals (Q95933694) (← links)