Genetic variation of glycophorins and infectious disease

por Hollox, Edward J., Louzada, Sandra
Publicado 2022

Directional and balancing selection in human beta-defensins

por Hollox, Edward J, Armour, John AL
Publicado 2008

Balancing selection at the human salivary agglutinin gene (DMBT1) driven by host-microbe interactions

por Alharbi, Adel F., Sheng, Nongfei, Nicol, Katie, Strömberg, Nicklas, Hollox, Edward J.
Publicado 2022

Copy Number Variation of the Beta Defensin Gene Cluster on Chromosome 8p Influences the Bacterial Microbiota within the Nasopharynx of Otitis-Prone Children

por Jones, Eric A., Kananurak, Anchasa, Bevins, Charles L., Hollox, Edward J., Bakaletz, Lauren O.
Publicado 2014

Determining multiallelic complex copy number and sequence variation from high coverage exome sequencing data

por Forni, Diego, Martin, Diana, Abujaber, Razan, Sharp, Andrew J., Sironi, Manuela, Hollox, Edward J.
Publicado 2015

Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer’s disease

por Kucukkilic, Ezgi, Brookes, Keeley, Barber, Imelda, Guetta-Baranes, Tamar, Morgan, Kevin, Hollox, Edward J.
Publicado 2018

Beta-defensin genomic copy number is not a modifier locus for cystic fibrosis

por Hollox, Edward J, Davies, Jane, Griesenbach, Uta, Burgess, Juliana, Alton, Eric WFW, Armour, John AL
Publicado 2005

Analysis of copy number variation at DMBT1 and age-related macular degeneration

por Polley, Shamik, Cipriani, Valentina, Khan, Jane C., Shahid, Humma, Moore, Anthony T., Yates, John R. W., Hollox, Edward J.
Publicado 2016

Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats

por Armour, John A. L., Palla, Raquel, Zeeuwen, Patrick L. J. M., den Heijer, Martin, Schalkwijk, Joost, Hollox, Edward J.
Publicado 2007

Copy-number variation of the neuronal glucose transporter gene SLC2A3 and age of onset in Huntington's disease

por Vittori, Angelica, Breda, Carlo, Repici, Mariaelena, Orth, Michael, Roos, Raymund A.C., Outeiro, Tiago F., Giorgini, Flaviano, Hollox, Edward J.
Publicado 2014

A 4q35.2 subtelomeric deletion identified in a screen of patients with co-morbid psychiatric illness and mental retardation

por Pickard, Ben S, Hollox, Edward J, Malloy, M Pat, Porteous, David J, Blackwood, Douglas HR, Armour, John AL, Muir, Walter J
Publicado 2004

Exome-wide analysis of copy number variation shows association of the human leukocyte antigen region with asthma in UK Biobank

por Fawcett, Katherine A., Demidov, German, Shrine, Nick, Paynton, Megan L., Ossowski, Stephan, Sayers, Ian, Wain, Louise V., Hollox, Edward J.
Publicado 2022

Human intelectin‐2 (ITLN2) is selectively expressed by secretory Paneth cells

por Nonnecke, Eric B., Castillo, Patricia A., Johansson, Malin E. V., Hollox, Edward J., Shen, Bo, Lönnerdal, Bo, Bevins, Charles L.
Publicado 2022

Human beta defensin (HBD) gene copy number affects HBD2 protein levels: impact on cervical bactericidal immunity in pregnancy

por James, Catherine P., Bajaj-Elliott, Mona, Abujaber, Razan, Forya, Frida, Klein, Nigel, David, Anna L., Hollox, Edward J., Peebles, Donald M.
Publicado 2018

Haptoglobin (HP) and Haptoglobin-related protein (HPR) copy number variation, natural selection, and trypanosomiasis

por Hardwick, Robert J., Ménard, Anne, Sironi, Manuela, Milet, Jacqueline, Garcia, André, Sese, Claude, Yang, Fengtang, Fu, Beiyuan, Courtin, David, Hollox, Edward J.
Publicado 2013

Understanding the Genomic Structure of Copy‐Number Variation of the Low‐Affinity Fcγ Receptor Region Allows Confirmation of the Association of FCGR3B Deletion with Rheumatoid Arthr...

por Rahbari, Raheleh, Zuccherato, Luciana W, Tischler, German, Chihota, Belinda, Ozturk, Hasret, Saleem, Sara, Tarazona‐Santos, Eduardo, Machado, Lee R, Hollox, Edward J
Publicado 2017

The Malaria-Protective Human Glycophorin Structural Variant DUP4 Shows Somatic Mosaicism and Association with Hemoglobin Levels

por Algady, Walid, Louzada, Sandra, Carpenter, Danielle, Brajer, Paulina, Färnert, Anna, Rooth, Ingegerd, Ngasala, Billy, Yang, Fengtang, Shaw, Marie-Anne, Hollox, Edward J.
Publicado 2018

Automated design of paralogue ratio test assays for the accurate and rapid typing of copy number variation

por Veal, Colin D., Xu, Hang, Reekie, Katherine, Free, Robert, Hardwick, Robert J., McVey, David, Brookes, Anthony J., Hollox, Edward J., Talbot, Christopher J.
Publicado 2013

Human CCL3L1 copy number variation, gene expression, and the role of the CCL3L1-CCR5 axis in lung function

por Adewoye, Adeolu B., Shrine, Nick, Odenthal-Hesse, Linda, Welsh, Samantha, Malarstig, Anders, Jelinsky, Scott, Kilty, Iain, Tobin, Martin D., Hollox, Edward J., Wain, Louise V.
Publicado 2018

Extensive variation in the intelectin gene family in laboratory and wild mouse strains

por Almalki, Faisal, Nonnecke, Eric B., Castillo, Patricia A., Bevin-Holder, Alex, Ullrich, Kristian K., Lönnerdal, Bo, Odenthal-Hesse, Linda, Bevins, Charles L., Hollox, Edward J.
Publicado 2021