Literature DB >> 35587224

Molecular Quantitative Trait Locus Mapping in Human Complex Diseases.

Oluwatosin A Olayinka1,2, Nicholas K O'Neill1,2, Lindsay A Farrer1,2,3,4,5,6, Gao Wang7,8, Xiaoling Zhang1,2,5.   

Abstract

Mapping quantitative trait loci (QTLs) for molecular traits from chromatin to metabolites (i.e., xQTLs) provides insight into the locations and effect modes of genetic variants that influence these molecular phenotypes and the propagation of functional consequences of each variant. xQTL studies indirectly interrogate the functional landscape of the molecular basis of complex diseases, including the impact of non-coding regulatory variants, the tissue specificity of regulatory elements, and their contribution to disease by integrating with genome-wide association studies (GWAS). We summarize a variety of molecular xQTL studies in human tissues and cells. In addition, using the Alzheimer's Disease Sequencing Project (ADSP) as an example, we describe the ADSP xQTL project, a collaborative effort across the ADSP Functional Genomics Consortium (ADSP-FGC). The project's ultimate goal is a reference map of Alzheimer's-related QTLs using existing datasets from multiple omics layers to help us study the consequences of genetic variants identified in the ADSP. xQTL studies enable the identification of the causal genes and pathways in GWAS loci, which will likely aid in the discovery of novel biomarkers and therapeutic targets for complex diseases.
© 2022 Wiley Periodicals LLC. © 2022 Wiley Periodicals LLC.

Entities:  

Keywords:  complex human diseases; molecular traits; xQTLs

Mesh:

Year:  2022        PMID: 35587224      PMCID: PMC9186089          DOI: 10.1002/cpz1.426

Source DB:  PubMed          Journal:  Curr Protoc        ISSN: 2691-1299


  92 in total

1.  Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets.

Authors:  Zhihong Zhu; Futao Zhang; Han Hu; Andrew Bakshi; Matthew R Robinson; Joseph E Powell; Grant W Montgomery; Michael E Goddard; Naomi R Wray; Peter M Visscher; Jian Yang
Journal:  Nat Genet       Date:  2016-03-28       Impact factor: 38.330

2.  A Bayesian framework for multiple trait colocalization from summary association statistics.

Authors:  Claudia Giambartolomei; Jimmy Zhenli Liu; Wen Zhang; Mads Hauberg; Huwenbo Shi; James Boocock; Joe Pickrell; Andrew E Jaffe; Bogdan Pasaniuc; Panos Roussos
Journal:  Bioinformatics       Date:  2018-08-01       Impact factor: 6.937

3.  Integrative approaches for large-scale transcriptome-wide association studies.

Authors:  Alexander Gusev; Arthur Ko; Huwenbo Shi; Gaurav Bhatia; Wonil Chung; Brenda W J H Penninx; Rick Jansen; Eco J C de Geus; Dorret I Boomsma; Fred A Wright; Patrick F Sullivan; Elina Nikkola; Marcus Alvarez; Mete Civelek; Aldons J Lusis; Terho Lehtimäki; Emma Raitoharju; Mika Kähönen; Ilkka Seppälä; Olli T Raitakari; Johanna Kuusisto; Markku Laakso; Alkes L Price; Päivi Pajukanta; Bogdan Pasaniuc
Journal:  Nat Genet       Date:  2016-02-08       Impact factor: 38.330

4.  Nonsense-mediated decay is highly stable across individuals and tissues.

Authors:  Nicole A Teran; Daniel C Nachun; Tiffany Eulalio; Nicole M Ferraro; Craig Smail; Manuel A Rivas; Stephen B Montgomery
Journal:  Am J Hum Genet       Date:  2021-07-02       Impact factor: 11.025

5.  Genetic Drivers of Epigenetic and Transcriptional Variation in Human Immune Cells.

Authors:  Lu Chen; Bing Ge; Francesco Paolo Casale; Louella Vasquez; Tony Kwan; Diego Garrido-Martín; Stephen Watt; Ying Yan; Kousik Kundu; Simone Ecker; Avik Datta; David Richardson; Frances Burden; Daniel Mead; Alice L Mann; Jose Maria Fernandez; Sophia Rowlston; Steven P Wilder; Samantha Farrow; Xiaojian Shao; John J Lambourne; Adriana Redensek; Cornelis A Albers; Vyacheslav Amstislavskiy; Sofie Ashford; Kim Berentsen; Lorenzo Bomba; Guillaume Bourque; David Bujold; Stephan Busche; Maxime Caron; Shu-Huang Chen; Warren Cheung; Oliver Delaneau; Emmanouil T Dermitzakis; Heather Elding; Irina Colgiu; Frederik O Bagger; Paul Flicek; Ehsan Habibi; Valentina Iotchkova; Eva Janssen-Megens; Bowon Kim; Hans Lehrach; Ernesto Lowy; Amit Mandoli; Filomena Matarese; Matthew T Maurano; John A Morris; Vera Pancaldi; Farzin Pourfarzad; Karola Rehnstrom; Augusto Rendon; Thomas Risch; Nilofar Sharifi; Marie-Michelle Simon; Marc Sultan; Alfonso Valencia; Klaudia Walter; Shuang-Yin Wang; Mattia Frontini; Stylianos E Antonarakis; Laura Clarke; Marie-Laure Yaspo; Stephan Beck; Roderic Guigo; Daniel Rico; Joost H A Martens; Willem H Ouwehand; Taco W Kuijpers; Dirk S Paul; Hendrik G Stunnenberg; Oliver Stegle; Kate Downes; Tomi Pastinen; Nicole Soranzo
Journal:  Cell       Date:  2016-11-17       Impact factor: 41.582

6.  Integrated genome-wide analysis of expression quantitative trait loci aids interpretation of genomic association studies.

Authors:  Roby Joehanes; Xiaoling Zhang; Tianxiao Huan; Chen Yao; Sai-Xia Ying; Quang Tri Nguyen; Cumhur Yusuf Demirkale; Michael L Feolo; Nataliya R Sharopova; Anne Sturcke; Alejandro A Schäffer; Nancy Heard-Costa; Han Chen; Po-Ching Liu; Richard Wang; Kimberly A Woodhouse; Kahraman Tanriverdi; Jane E Freedman; Nalini Raghavachari; Josée Dupuis; Andrew D Johnson; Christopher J O'Donnell; Daniel Levy; Peter J Munson
Journal:  Genome Biol       Date:  2017-01-25       Impact factor: 13.583

7.  Genome-wide identification of splicing QTLs in the human brain and their enrichment among schizophrenia-associated loci.

Authors:  Atsushi Takata; Naomichi Matsumoto; Tadafumi Kato
Journal:  Nat Commun       Date:  2017-02-27       Impact factor: 14.919

8.  RNA splicing is a primary link between genetic variation and disease.

Authors:  Yang I Li; Bryce van de Geijn; Anil Raj; David A Knowles; Allegra A Petti; David Golan; Yoav Gilad; Jonathan K Pritchard
Journal:  Science       Date:  2016-04-28       Impact factor: 47.728

9.  CFIm25 links alternative polyadenylation to glioblastoma tumour suppression.

Authors:  Chioniso P Masamha; Zheng Xia; Jingxuan Yang; Todd R Albrecht; Min Li; Ann-Bin Shyu; Wei Li; Eric J Wagner
Journal:  Nature       Date:  2014-05-11       Impact factor: 49.962

10.  An xQTL map integrates the genetic architecture of the human brain's transcriptome and epigenome.

Authors:  Bernard Ng; Charles C White; Hans-Ulrich Klein; Solveig K Sieberts; Cristin McCabe; Ellis Patrick; Jishu Xu; Lei Yu; Chris Gaiteri; David A Bennett; Sara Mostafavi; Philip L De Jager
Journal:  Nat Neurosci       Date:  2017-09-04       Impact factor: 24.884

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