All papers authored by Xiao-Qing Liu
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Xiao-Qing Liu
Survival-Related Genes on Chromosomes 6 and 17 in Medulloblastoma
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Omange Rw,
Binhua Liang ,
Nikki Toledo,
Yan Hai,
Lewis R. Liu,
Dane Schalk ,
Liu Lr,
Tamara G. Dacoba ,
Jose Crecente-Campo ,
Andrew B. Lambe,
So-Yon Lim ,
Mohammad Abul Kashem ,
Dacoba Tg
and 16 other authors
Vaccine targeting SIVmac251 protease cleavage sites protects macaques against vaginal infection
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Elizabeth Wall-Wieler,
Chelsea A. Ruth,
Xiaoqing Liu ,
Leslie L. Roos
Revisiting the association between maternal and offspring preterm birth using a sibling design
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Jillian Fazio,
Pingzhao Hu,
Andrew D. Paterson
Identity-by-descent mapping for diastolic blood pressure in unrelated Mexican Americans
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Julia N. Bailey
Filtering genetic variants and placing informative priors based on putative biological function
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Andrew D. Paterson,
Terry Bennett
Measurement equivalence of the autism symptom phenotype in children and youth
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Individual common variants exert weak effects on the risk for autism spectrum disorders.
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Marion E. Reid
ABCG2 null alleles define the Jr(a-) blood group phenotype
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Stelios Georgiades,
Eric Duku,
Ann Thompson,
Bernie Devlin,
Edwin H. Cook,
Ellen M. Wijsman,
Andrew D. Paterson,
Peter Szatmari
Identification of Genetic Loci Underlying the Phenotypic Constructs of Autism Spectrum Disorders
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Brett S. Abrahams,
Joana Almeida,
Elena Bacchelli,
Gary D. Bader,
Anthony J. Bailey,
Gillian Baird
and 163 other authors
Functional impact of global rare copy number variation in autism spectrum disorders
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Brett S. Abrahams,
Nuala Sykes,
Alistair T. Pagnamenta,
Joana Almeida,
Elena Bacchelli,
Anthony J. Bailey,
Gillian Baird
and 156 other authors
A genome-wide scan for common alleles affecting risk for autism
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A Genome-Wide Linkage and Association Scan Reveals Novel Loci for Autism
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Andrew D. Paterson,
Ning He,
Peter St. George-Hyslop,
Virpi Rauta,
Carola Gronhagen-Riska,
Markku Laakso,
Lise Thibaudin,
Francois Berthoux,
Daniel Cattran,
York Pei
IL5RA and TNFRSF6B Gene Variants Are Associated With Sporadic IgA Nephropathy
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