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| Open AccessGenome-wide association mapping for dominance effects in female fertility using real and simulated data from Danish Holstein cattle
- Xiaowei Mao
- , Goutam Sahana
- & Bernt Guldbrandtsen
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| Open AccessPrevalence and association of single nucleotide polymorphisms with sarcopenia in older women depends on definition
- Praval Khanal
- , Lingxiao He
- & Christopher I. Morse
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| Open AccessA genetic analysis identifies a haplotype at adiponectin locus: Association with obesity and type 2 diabetes
- Sayantani Pramanik Palit
- , Roma Patel
- & Rasheedunnisa Begum
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| Open AccessGenome-Wide Association Study of VKORC1 and CYP2C9 on acenocoumarol dose, stroke recurrence and intracranial haemorrhage in Spain
- Natalia Cullell
- , Caty Carrera
- & Jerzy Krupinski
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| Open AccessThe role of control region mitochondrial DNA mutations in cardiovascular disease: stroke and myocardial infarction
- Miriam Umbria
- , Amanda Ramos
- & Cristina Santos
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| Open AccessGenotype-independent association between vitamin D deficiency and polycystic ovarian syndrome in Lahore, Pakistan
- Nasira M. Lone
- , Saba Riaz
- & Adrian R. Martineau
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| Open AccessAATF and SMARCA2 are associated with thyroid volume in Hashimoto’s thyroiditis patients
- Luka Brčić
- , Ana Barić
- & Vesna Boraska Perica
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| Open AccessA transcriptome-wide association study based on 27 tissues identifies 106 genes potentially relevant for disease pathology in age-related macular degeneration
- Tobias Strunz
- , Susette Lauwen
- & Bernhard H. F. Weber
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| Open AccessGenome-Wide Association Study of Brain Connectivity Changes for Alzheimer’s Disease
- Samar S. M. Elsheikh
- , Emile R. Chimusa
- & Alessandro Crimi
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| Open AccessPhenome-wide functional dissection of pleiotropic effects highlights key molecular pathways for human complex traits
- Anton E. Shikov
- , Rostislav K. Skitchenko
- & Yury A. Barbitoff
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| Open AccessThe Asthma-associated PER1-like domain-containing protein 1 (PERLD1) Haplotype Influences Soluble Glycosylphosphatidylinositol Anchor Protein (sGPI-AP) Levels in Serum and Immune Cell Proliferation
- Yang Yie Sio
- , Ramani Anantharaman
- & Fook Tim Chew
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| Open AccessThe interaction of Multiple Sclerosis risk loci with Epstein-Barr virus phenotypes implicates the virus in pathogenesis
- Ali Afrasiabi
- , Grant P. Parnell
- & David R. Booth
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| Open AccessGenome-wide association study identifies novel risk variants from RPS6KA1, CADPS, VARS, and DHX58 for fasting plasma glucose in Arab population
- Prashantha Hebbar
- , Mohamed Abu-Farha
- & Thangavel Alphonse Thanaraj
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| Open AccessGenetic Variants Associated with Chronic Kidney Disease in a Spanish Population
- Zuray Corredor
- , Miguel Inácio da Silva Filho
- & Susana Pastor
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| Open AccessMetabolic GWAS of elite athletes reveals novel genetically-influenced metabolites associated with athletic performance
- Fatima Al-Khelaifi
- , Ilhame Diboun
- & Mohamed A. Elrayess
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| Open AccessGenome-wide human brain eQTLs: In-depth analysis and insights using the UKBEC dataset
- Letitia M. F. Sng
- , Peter C. Thomson
- & Daniah Trabzuni
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| Open AccessThe FTO gene polymorphism rs9939609 is associated with obesity and disability in multiple sclerosis patients
- Ahmad Al-Serri
- , Raed Alroughani
- & Rabeah A. Al-Temaimi
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| Open AccessGenome investigations show host adaptation and transmission of LA-MRSA CC398 from pigs into Danish healthcare institutions
- Raphael Niklaus Sieber
- , Anders Rhod Larsen
- & Marc Stegger
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| Open AccessPolymorphisms of MFGE8 are associated with susceptibility and clinical manifestations through gene expression modulation in Koreans with systemic lupus erythematosus
- Wook-Young Baek
- , Ji-Min Woo
- & Chang-Hee Suh
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| Open AccessThe myopia susceptibility locus vasoactive intestinal peptide receptor 2 (VIPR2) contains variants with opposite effects
- Kim Hung Leung
- , Shumeng Luo
- & Shea Ping Yip
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| Open AccessGenetics of cognitive trajectory in Brazilians: 15 years of follow-up from the Bambuí-Epigen Cohort Study of Aging
- Mateus H. Gouveia
- , Cibele C. Cesar
- & Maria Fernanda Lima-Costa
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| Open AccessTSLRF: Two-Stage Algorithm Based on Least Angle Regression and Random Forest in genome-wide association studies
- Jiali Sun
- , Qingtai Wu
- & Jin Zhang
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| Open AccessFine mapping and identification of serum urate loci in American Indians: The Strong Heart Family Study
- Geetha Chittoor
- , Karin Haack
- & V. S. Voruganti
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| Open AccessAssociation between impulsivity traits and body mass index at the observational and genetic epidemiology level
- David Meyre
- , Sebat Mohamed
- & Harriet de Wit
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| Open AccessGenome Wide Analysis Approach Suggests Chromosome 2 Locus to be Associated with Thiazide and Thiazide Like-Diuretics Blood Pressure Response
- Sonal Singh
- , Caitrin W. McDonough
- & Julie A. Johnson
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| Open AccessAn exome-wide rare variant analysis of Korean men identifies three novel genes predisposing to prostate cancer
- Jong Jin Oh
- , Manu Shivakumar
- & Seok-Soo Byun
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| Open AccessContribution of rare coding mutations in CD36 to type 2 diabetes and cardio-metabolic complications
- David Meyre
- , Edward J. Andress
- & Kenneth J. Linton
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| Open AccessValidation of a priori candidate Alzheimer’s disease SNPs with brain amyloid-beta deposition
- Michael Vacher
- , Tenielle Porter
- & Simon M. Laws
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| Open AccessImproved power and precision with whole genome sequencing data in genome-wide association studies of inflammatory biomarkers
- Julia Höglund
- , Nima Rafati
- & Åsa Johansson
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| Open AccessAssociation of NCF1 polymorphism with systemic lupus erythematosus and systemic sclerosis but not with ANCA-associated vasculitis in a Japanese population
- Nozomi Yokoyama
- , Aya Kawasaki
- & Naoyuki Tsuchiya
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| Open AccessIdentification of HLA-A*02:06:01 as the primary disease susceptibility HLA allele in cold medicine-related Stevens-Johnson syndrome with severe ocular complications by high-resolution NGS-based HLA typing
- Ken Nakatani
- , Mayumi Ueta
- & Katsushi Tokunaga
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| Open AccessAssociation study of AGO1 and AGO2 genes polymorphisms with recurrent pregnancy loss
- Young Ran Kim
- , Chang Soo Ryu
- & Nam Keun Kim
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| Open AccessExtreme sampling design in genetic association mapping of quantitative trait loci using balanced and unbalanced case-control samples
- Yi Li
- , Orna Levran
- & Chen Suo
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| Open AccessThe whole-genome sequence analysis of Morchella sextelata
- Mei-Han
- , Qingshan-Wang
- & Wuhanqimuge
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| Open AccessScrapie susceptibility-associated indel polymorphism of shadow of prion protein gene (SPRN) in Korean native black goats
- Yong-Chan Kim
- , Seon-Kwan Kim
- & Byung-Hoon Jeong
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| Open AccessAssociation of Fok1 VDR polymorphism with Vitamin D and its associated molecules in pulmonary tuberculosis patients and their household contacts
- Sudhasini Panda
- , Ambrish Tiwari
- & Archana Singh
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| Open AccessGenome-wide association meta-analysis identifies five novel loci for age-related hearing impairment
- Andries Paul Nagtegaal
- , Linda Broer
- & André Goedegebure
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| Open AccessGenome-wide association analysis of hippocampal volume identifies enrichment of neurogenesis-related pathways
- Emrin Horgusluoglu-Moloch
- , Shannon L. Risacher
- & Kristin Fargher
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| Open AccessImprovement of the Pacific bluefin tuna (Thunnus orientalis) reference genome and development of male-specific DNA markers
- Ayako Suda
- , Issei Nishiki
- & Atushi Fujiwara
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| Open AccessGenome-wide association study and whole-genome sequencing identify a deletion in LRIT3 associated with canine congenital stationary night blindness
- Rueben G. Das
- , Doreen Becker
- & Keiko Miyadera
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| Open AccessA variant of the castor zinc finger 1 (CASZ1) gene is differentially associated with the clinical classification of chronic venous disease
- Gregory T. Jones
- , Judith Marsman
- & Andre M. van Rij
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| Open AccessAssociation study identified biologically relevant receptor genes with synergistic functions in celiac disease
- Pratibha Banerjee
- , Sandilya Bhagavatula
- & Sabyasachi Senapati
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| Open AccessThe association of integration patterns of human papilloma virus and single nucleotide polymorphisms on immune- or DNA repair-related genes in cervical cancer patients
- Jungnam Joo
- , Yosuke Omae
- & Joo-Young Kim
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| Open AccessYeast PAF1 complex counters the pol III accumulation and replication stress on the tRNA genes
- Pratibha Bhalla
- , Ashutosh Shukla
- & Purnima Bhargava
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| Open AccessA Frameshift Variant in the CHST9 Gene Identified by Family-Based Whole Genome Sequencing Is Associated with Schizophrenia in Chinese Population
- Jingchun Chen
- , Jain-Shing Wu
- & Xiangning Chen
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| Open AccessThe genetic relationship between female reproductive traits and six psychiatric disorders
- Guiyan Ni
- , Azmeraw T. Amare
- & S. Hong Lee
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| Open AccessVariants Associated with the Ankle Brachial Index Differ by Hispanic/Latino Ethnic Group: a genome-wide association study in the Hispanic Community Health Study/Study of Latinos
- Tamar Sofer
- , Leslie Emery
- & Christina L. Wassel
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| Open AccessMitochondrial DNA sequencing reveals association of variants and haplogroup M33a2′3 with High altitude pulmonary edema susceptibility in Indian male lowlanders
- Swati Sharma
- , Sayar Singh
- & Yamini Singh
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| Open AccessGenetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia
- Luke W. Bonham
- , Natasha Z. R. Steele
- & A. B. Singleton