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No Evidence That Genetic Variation at the Klotho Locus Is Associated With Longevity in Caucasians from the Newcastle 85+ Study and the UK Biobank.
Published in:
2022
By:
- Amin, Hasnat A;
- Cordell, Heather J;
- Martin-Ruiz, Carmen;
- Robinson, Louise;
- Kirkwood, Tom;
- Blakemore, Alexandra I;
- Drenos, Fotios
Publication type:
journal article
Multitrait genome-wide analyses identify new susceptibility loci and candidate drugs to primary sclerosing cholangitis.
Published in:
Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-36678-8
By:
- Han, Younghun;
- Byun, Jinyoung;
- Zhu, Catherine;
- Sun, Ryan;
- Roh, Julia Y.;
- Cordell, Heather J.;
- Lee, Hyun-Sung;
- Shaw, Vikram R.;
- Kang, Sung Wook;
- Razjouyan, Javad;
- Cooley, Matthew A.;
- Hassan, Manal M.;
- Siminovitch, Katherine A.;
- Folseraas, Trine;
- Ellinghaus, David;
- Bergquist, Annika;
- Rushbrook, Simon M.;
- Franke, Andre;
- Karlsen, Tom H.;
- Lazaridis, Konstantinos N.
Publication type:
Article
Bayesian network analysis incorporating genetic anchors complements conventional Mendelian randomization approaches for exploratory analysis of causal relationships in complex data.
Published in:
PLoS Genetics, 2020, v. 16, n. 3, p. 1, doi. 10.1371/journal.pgen.1008198
By:
- Howey, Richard;
- Shin, So-Youn;
- Relton, Caroline;
- Davey Smith, George;
- Cordell, Heather J.
Publication type:
Article
The Plight of Muntaser Ibrahim.
Published in:
PLoS Genetics, 2019, v. 15, n. 3, p. 1, doi. 10.1371/journal.pgen.1008100
By:
- Sirugo, Giorgio;
- Williams, Scott M.;
- Tishkoff, Sarah A.;
- Cordell, Heather J.;
- Marchini, Jonathan;
- Barsh, Gregory S.;
- Copenhaver, Gregory P.
Publication type:
Article
Amino acid residues in five separate HLA genes can explain most of the known associations between the MHC and primary biliary cholangitis.
Published in:
PLoS Genetics, 2018, v. 14, n. 12, p. 1, doi. 10.1371/journal.pgen.1007833
By:
- Darlay, Rebecca;
- Ayers, Kristin L.;
- Cordell, Heather J.;
- Hall, Lynsey S.;
- Mells, George F.;
- Sandford, Richard N.;
- Liu, Jimmy Z.;
- Anderson, Carl A.;
- Almarri, Mohamed A.;
- Alexander, Graeme J.;
- Jones, David E.
Publication type:
Article
Statistical Modeling of Interlocus Interactions in a Complex Disease: Rejection of the...
Published in:
Genetics, 2001, v. 158, n. 1, p. 357, doi. 10.1093/genetics/158.1.357
By:
- Cordell, Heather J.;
- Todd, John A.;
- Hill, Natasha J.;
- Lord, Christopher J.;
- Lyons, Paul A.;
- Peterson, Laurence B.;
- Wicker, Linda S.;
- Clayton, David G.
Publication type:
Article
Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes.
Published in:
2021
By:
- Deelen, Joris;
- Evans, Daniel S.;
- Arking, Dan E.;
- Tesi, Niccolò;
- Nygaard, Marianne;
- Liu, Xiaomin;
- Wojczynski, Mary K.;
- Biggs, Mary L.;
- van der Spek, Ashley;
- Atzmon, Gil;
- Ware, Erin B.;
- Sarnowski, Chloé;
- Smith, Albert V.;
- Seppälä, Ilkka;
- Cordell, Heather J.;
- Dose, Janina;
- Amin, Najaf;
- Arnold, Alice M.;
- Ayers, Kristin L.;
- Barzilai, Nir
Publication type:
Correction Notice
A case–control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE).
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2019, v. 180, n. 1, p. 68, doi. 10.1002/ajmg.b.32708
By:
- Alblooshi, Hiba;
- Al Safar, Habiba;
- Fisher, Holly F.;
- Cordell, Heather J.;
- El Kashef, Ahmed;
- Al Ghaferi, Hamad;
- Shawky, Mansour;
- Reece, Stuart;
- Hulse, Gary K.;
- Tay, Guan K.
Publication type:
Article
Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Published in:
Nature Genetics, 2013, v. 45, n. 7, p. 822, doi. 10.1038/ng.2637
By:
- Cordell, Heather J;
- Bentham, Jamie;
- Topf, Ana;
- Zelenika, Diana;
- Heath, Simon;
- Mamasoula, Chrysovalanto;
- Cosgrove, Catherine;
- Blue, Gillian;
- Granados-Riveron, Javier;
- Setchfield, Kerry;
- Thornborough, Chris;
- Breckpot, Jeroen;
- Soemedi, Rachel;
- Martin, Ruairidh;
- Rahman, Thahira J;
- Hall, Darroch;
- van Engelen, Klaartje;
- Moorman, Antoon F M;
- Zwinderman, Aelko H;
- Barnett, Phil
Publication type:
Article
Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis.
Published in:
Nature Genetics, 2013, v. 45, n. 2, p. 208, doi. 10.1038/ng.2518
By:
- Fakiola, Michaela;
- Strange, Amy;
- Cordell, Heather J;
- Miller, E Nancy;
- Pirinen, Matti;
- Su, Zhan;
- Mishra, Anshuman;
- Mehrotra, Sanjana;
- Monteiro, Gloria R;
- Band, Gavin;
- Bellenguez, Céline;
- Dronov, Serge;
- Edkins, Sarah;
- Freeman, Colin;
- Giannoulatou, Eleni;
- Gray, Emma;
- Hunt, Sarah E;
- Lacerda, Henio G;
- Langford, Cordelia;
- Pearson, Richard
Publication type:
Article
Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.
Published in:
Nature Genetics, 2012, v. 44, n. 10, p. 1137, doi. 10.1038/ng.2395
By:
- Liu, Jimmy Z;
- Almarri, Mohamed A;
- Gaffney, Daniel J;
- Mells, George F;
- Jostins, Luke;
- Cordell, Heather J;
- Ducker, Samantha J;
- Day, Darren B;
- Heneghan, Michael A;
- Neuberger, James M;
- Donaldson, Peter T;
- Bathgate, Andrew J;
- Burroughs, Andrew;
- Davies, Mervyn H;
- Jones, David E;
- Alexander, Graeme J;
- Barrett, Jeffrey C;
- Sandford, Richard N;
- Anderson, Carl A
Publication type:
Article
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.
Published in:
2011
By:
- Mells, George F;
- Floyd, James A B;
- Morley, Katherine I;
- Cordell, Heather J;
- Franklin, Christopher S;
- Shin, So-Youn;
- Heneghan, Michael A;
- Neuberger, James M;
- Donaldson, Peter T;
- Day, Darren B;
- Ducker, Samantha J;
- Muriithi, Agnes W;
- Wheater, Elizabeth F;
- Hammond, Christopher J;
- Dawwas, Muhammad F;
- Jones, David E;
- Peltonen, Leena;
- Alexander, Graeme J;
- Sandford, Richard N;
- Anderson, Carl A
Publication type:
Correction Notice
Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.
Published in:
Nature Genetics, 2011, v. 43, n. 4, p. 329, doi. 10.1038/ng.789
By:
- Mells, George F.;
- Floyd, James A. B.;
- Morley, Katherine I.;
- Cordell, Heather J.;
- Franklin, Christopher S.;
- So-Youn Shin;
- Heneghan, Michael A.;
- Neuberger, James M.;
- Donaldson, Peter T.;
- Day, Darren B.;
- Ducker, Samantha J.;
- Muriithi, Agnes W.;
- Wheater, Elizabeth F.;
- Hammond, Christopher J.;
- Dawwas, Muhammad F.;
- Jones, David E.;
- Peltonen, Leena;
- Alexander, Graeme J.;
- Sandford, Richard N.;
- Anderson, Carl A.
Publication type:
Article
Reply to “Associations of CFHR1–CFHR3 deletion and a CFH SNP to age-related macular degeneration are not independent”.
Published in:
2010
By:
- Hughes, Anne E;
- Orr, Nick;
- Cordell, Heather J;
- Goodship, Timothy
Publication type:
Letter
HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin.
Published in:
Nature Genetics, 2009, v. 41, n. 7, p. 816, doi. 10.1038/ng.379
By:
- Daly, Ann K.;
- Donaldson, Peter T.;
- Bhatnagar, Pallav;
- Shen, Yufeng;
- Pe'er, Itsik;
- Floratos, Aris;
- Daly, Mark J.;
- Goldstein, David B.;
- John, Sally;
- Nelson, Matthew R.;
- Graham, Julia;
- Park, B. Kevin;
- Dillon, John F.;
- Bernal, William;
- Cordell, Heather J.;
- Pirmohamed, Munir;
- Aithal, Guruprasad P.;
- Day, Christopher P.
Publication type:
Article
Haplotype tagging for the identification of common disease genes.
Published in:
Nature Genetics, 2001, v. 29, n. 2, p. 233, doi. 10.1038/ng1001-233
By:
- Johnson, Gillian C.L.;
- Esposito, Laura;
- Barratt, Bryan J.;
- Smith, Annabel N.;
- Heward, Joanne;
- Di Genova, Gianfranco;
- Ueda, Hironori;
- Cordell, Heather J.;
- Eaves, Iain A.;
- Dudbridge, Frank;
- Twells, Rebecca C.J.;
- Payne, Felicity;
- Hughes, Wil;
- Nutland, Sarah;
- Stevens, Helen;
- Carr, Phillipa;
- Tuomilehto-Wolf, Eva;
- Tuomilehto, Jaakko;
- Gough, Stephen C.L.
Publication type:
Article
A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans.
Published in:
2016
By:
- Pazderska, Agnieszka;
- Oftedal, Bergithe E;
- Napier, Catherine M;
- Ainsworth, Holly F;
- Husebye, Eystein S;
- Cordell, Heather J;
- Pearce, Simon Hs;
- Mitchell, Anna L;
- Pearce, Simon H S
Publication type:
journal article
Correction: Linkage Analysis in Autoimmune Addison’s Disease: NFATC1 as a Potential Novel Susceptibility Locus.
Published in:
PLoS ONE, 2015, v. 10, n. 9, p. 1, doi. 10.1371/journal.pone.0138844
By:
- Mitchell, Anna L.;
- Bøe Wolff, Anette;
- MacArthur, Katie;
- Weaver, Jolanta U.;
- Vaidya, Bijay;
- null, null;
- Erichsen, Martina M.;
- Darlay, Rebecca;
- Husebye, Eystein S.;
- Cordell, Heather J.;
- Pearce, Simon H. S.
Publication type:
Article
Linkage Analysis in Autoimmune Addison’s Disease: NFATC1 as a Potential Novel Susceptibility Locus.
Published in:
PLoS ONE, 2015, v. 10, n. 6, p. 1, doi. 10.1371/journal.pone.0123550
By:
- Mitchell, Anna L.;
- Bøe Wolff, Anette;
- MacArthur, Katie;
- Weaver, Jolanta U.;
- Vaidya, Bijay;
- null, null;
- Erichsen, Martina M.;
- Darlay, Rebecca;
- Husebye, Eystein S.;
- Cordell, Heather J.;
- Pearce, Simon H. S.
Publication type:
Article
First Genome-Wide Association Study in an Australian Aboriginal Population Provides Insights into Genetic Risk Factors for Body Mass Index and Type 2 Diabetes.
Published in:
PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0119333
By:
- Anderson, Denise;
- Cordell, Heather J.;
- Fakiola, Michaela;
- Francis, Richard W.;
- Syn, Genevieve;
- Scaman, Elizabeth S. H.;
- Davis, Elizabeth;
- Miles, Simon J.;
- McLeay, Toby;
- Jamieson, Sarra E.;
- Blackwell, Jenefer M.
Publication type:
Article
Determining the Population Frequency of the <i>CFHR3/CFHR1</i> Deletion at 1q32.
Published in:
PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0060352
By:
- Holmes, Lucy V.;
- Strain, Lisa;
- Staniforth, Scott J.;
- Moore, Iain;
- Marchbank, Kevin;
- Kavanagh, David;
- Goodship, Judith A.;
- Cordell, Heather J.;
- Goodship, Timothy H. J.
Publication type:
Article
Genetic Variation in VEGF Does Not Contribute Significantly to the Risk of Congenital Cardiovascular Malformation.
Published in:
PLoS ONE, 2009, v. 4, n. 3, p. 1, doi. 10.1371/journal.pone.0004978
By:
- Griffin, Helen R.;
- Hall, Darroch H.;
- Topf, Ana;
- Eden, James;
- Stuart, A. Graham;
- Parsons, Jonathan;
- Peart, Ian;
- Deanfield, John E.;
- O'Sullivan, John;
- Babu-Narayan, Sonya V.;
- Gatzoulis, Michael A.;
- Bu'Lock, Frances A.;
- Bhattacharya, Shoumo;
- Bentham, Jamie;
- Farrall, Martin;
- Riveron, Javier Granados;
- Brook, J. David;
- Burn, John;
- Cordell, Heather J.;
- Goodship, Judith A.
Publication type:
Article
Genetic and Epigenetic Factors at COL2A1 and ABCA4 Influence Clinical Outcome in Congenital Toxoplasmosis.
Published in:
PLoS ONE, 2008, v. 3, n. 6, p. 1, doi. 10.1371/journal.pone.0002285
By:
- Jamieson, Sarra E.;
- de Roubaix, Lee-Anne;
- Cortina-Borja, Mario;
- Hooi Kuan Tan;
- Mui, Ernest J.;
- Cordell, Heather J.;
- Kirisits, Michael J.;
- Miller, E. Nancy;
- Peacock, Christopher S.;
- Hargrave, Aubrey C.;
- Coyne, Jessica J.;
- Boyer, Kenneth;
- Bessieres, Marie-Hélène;
- Buffolano, Wilma;
- Ferret, Nicole;
- Franck, Jacqueline;
- Kieffer, François;
- Meier, Paul;
- Nowakowska, Dorota E.;
- Paul, Malgorzata
Publication type:
Article
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility.
Published in:
2009
By:
- Mitchell, Anna L;
- Cordell, Heather J;
- Soemedi, Rachel;
- Owen, Kate;
- Skinningsrud, Beate;
- Wolff, Anette Bøe;
- Ericksen, Martina;
- Undlien, Dag;
- Husebye, Eystein;
- Pearce, Simon H S
Publication type:
journal article
Genomic polymorphism at the interferon-induced helicase (IFIH1) locus contributes to Graves' disease susceptibility.
Published in:
2007
By:
- Sutherland, Alison;
- Davies, Jocelyn;
- Owen, Catherine J;
- Vaikkakara, Suresh;
- Walker, Christine;
- Cheetham, Timothy D;
- James, R Andrew;
- Perros, Petros;
- Donaldson, Peter T;
- Cordell, Heather J;
- Quinton, Richard;
- Pearce, Simon H S
Publication type:
journal article
Association between aldosterone production and variation in the 11beta-hydroxylase (CYP11B1) gene.
Published in:
2006
By:
- Imrie, Helen;
- Freel, Marie;
- Mayosi, Bongani M;
- Davies, Eleanor;
- Fraser, Robert;
- Ingram, Mary;
- Cordell, Heather J;
- Farrall, Martin;
- Avery, Peter J;
- Watkins, Hugh;
- Keavney, Bernard;
- Connell, John M C
Publication type:
journal article
Absolute Risk of Childhood-Onset Type 1 Diabetes Defined by Human Leukocyte Antigen Class II Genotype: A Population-Based Study in the United Kingdom.
Published in:
Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 8, p. 4037, doi. 10.1210/jc.2003-032084
By:
- LAMBERT, A. PAUL;
- GILLESPIE, KATHLEEN M.;
- THOMSON, GLENYS;
- CORDELL, HEATHER J.;
- TODD, JOHN A.;
- GALE, EDWIN A. M.;
- BINGLEY, POLLY J.
Publication type:
Article
Detecting gene-gene interactions that underlie human diseases.
Published in:
2009
By:
- Cordell, Heather J.
Publication type:
journal article
Linkage and association mapping of the LRP5 locus on chromosome 11q13 in type 1 diabetes.
Published in:
Human Genetics, 2003, v. 113, n. 2, p. 99, doi. 10.1007/s00439-003-0940-6
By:
- Twells, Rebecca C. J.;
- Mein, Charles A.;
- Payne, Felicity;
- Veijola, Riitta;
- Gilbey, Matthew;
- Bright, Matthew;
- Timms, Andrew;
- Nakagawa, Yusuke;
- Snook, Hywel;
- Nutland, Sarah;
- Rance, Helen E.;
- Carr, Philippa;
- Dudbridge, Frank;
- Cordell, Heather J.;
- Cooper, Jason;
- Tuomilehto-Wolf, Eva;
- Tuomilehto, Jaakko;
- Phillips, Michael;
- Metzker, Michael;
- Hess, J. Fred
Publication type:
Article
A meta-analysis of genome-wide association studies identifies multiple longevity genes.
Published in:
Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-11558-2
By:
- Deelen, Joris;
- Evans, Daniel S.;
- Arking, Dan E.;
- Tesi, Niccolò;
- Nygaard, Marianne;
- Liu, Xiaomin;
- Wojczynski, Mary K.;
- Biggs, Mary L.;
- van der Spek, Ashley;
- Atzmon, Gil;
- Ware, Erin B.;
- Sarnowski, Chloé;
- Smith, Albert V.;
- Seppälä, Ilkka;
- Cordell, Heather J.;
- Dose, Janina;
- Amin, Najaf;
- Arnold, Alice M.;
- Ayers, Kristin L.;
- Barzilai, Nir
Publication type:
Article
A PDCD1 Role in the Genetic Predisposition to NAFLD-HCC?
Published in:
Cancers, 2021, v. 13, n. 6, p. 1412, doi. 10.3390/cancers13061412
By:
- Eldafashi, Nardeen;
- Darlay, Rebecca;
- Shukla, Ruchi;
- McCain, Misti Vanette;
- Watson, Robyn;
- Liu, Yang Lin;
- McStraw, Nikki;
- Fathy, Moustafa;
- Fawzy, Michael Atef;
- Zaki, Marco Y. W.;
- Daly, Ann K.;
- Maurício, João P.;
- Burt, Alastair D.;
- Haugk, Beate;
- Cordell, Heather J.;
- Bianco, Cristiana;
- Dufour, Jean-François;
- Valenti, Luca;
- Anstee, Quentin M.;
- Reeves, Helen L.
Publication type:
Article
A composite-likelihood approach for identifying polymorphisms that are potentially directly associated with disease.
Published in:
European Journal of Human Genetics, 2009, v. 17, n. 5, p. 644, doi. 10.1038/ejhg.2008.242
By:
- Biernacka, Joanna M.;
- Cordell, Heather J.
Publication type:
Article
PREMIM and EMIM: tools for estimation of maternal, imprinting and interaction effects using multinomial modelling.
Published in:
BMC Bioinformatics, 2012, v. 13, n. 1, p. 149, doi. 10.1186/1471-2105-13-149
By:
- Howey, Richard;
- Cordell, Heather J
Publication type:
Article
Marked variation in heritability estimates of left ventricular mass depending on modality of measurement.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-49961-w
By:
- Nethononda, Richard M.;
- McGurk, Kathryn A.;
- Whitworth, Polly;
- Francis, Jane;
- Mamasoula, Chysovalanto;
- Cordell, Heather J.;
- Neubauer, Stefan;
- Keavney, Bernard D.;
- Mayosi, Bongani M.;
- Farrall, Martin;
- Watkins, Hugh
Publication type:
Article
Using penalized regression to predict phenotype from SNP data.
Published in:
BMC Proceedings, 2018, v. 12, n. 9, p. N.PAG, doi. 10.1186/s12919-018-0149-2
By:
- Cherlin, Svetlana;
- Howey, Richard A. J.;
- Cordell, Heather J.
Publication type:
Article
Application of Bayesian networks to GAW20 genetic and blood lipid data.
Published in:
BMC Proceedings, 2018, v. 12, n. 9, p. N.PAG, doi. 10.1186/s12919-018-0116-y
By:
- Howey, Richard A. J.;
- Cordell, Heather J.
Publication type:
Article
A Genome-Wide Search for Type 2 Diabetes Susceptibility Genes in an Extended Arab Family.
Published in:
Annals of Human Genetics, 2013, v. 77, n. 6, p. 488, doi. 10.1111/ahg.12036
By:
- Al Safar, Habiba S.;
- Cordell, Heather J.;
- Jafer, Osman;
- Anderson, Denise;
- Jamieson, Sarra E.;
- Fakiola, Michaela;
- Khazanehdari, Kamal;
- Tay, Guan K.;
- Blackwell, Jenefer M.
Publication type:
Article
DNA methylation abnormalities at gene promoters are extensive and variable in the elderly and phenocopy cancer cells.
Published in:
FASEB Journal, 2014, v. 28, n. 7, p. 3261, doi. 10.1096/fj.13-246173
By:
- Gautrey, Hannah E.;
- van Otterdijk, Sanne D.;
- Cordell, Heather J.;
- Mathers, John C.;
- Strathdee, Gordon
Publication type:
Article
Gene expression in large pedigrees: analytic approaches.
Published in:
BMC Genetics, 2016, v. 17, p. 13, doi. 10.1186/s12863-015-0311-z
By:
- Cantor, Rita M.;
- Cordell, Heather J.
Publication type:
Article
A genome-wide scan for type 1 diabetes susceptibility genes innuclear families with multiple affected siblings in Finland.
Published in:
BMC Genetics, 2007, v. 8, p. 84, doi. 10.1186/1471-2156-8-84
By:
- Qing Qiao;
- Österholm, Anne-May;
- Bing He;
- Pitkäniemi, Janne;
- Cordell, Heather J.;
- Sarti, Cinzia;
- Kinnunen, Leena;
- Tuomilehto-Wolf, Eva;
- Tryggvason, Karl;
- Tuomilehto, Jaakko
Publication type:
Article
Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans.
Published in:
BMC Genetics, 2005, v. 6, p. S1, doi. 10.1186/1471-2156-6-S1-S1
By:
- Bailey-Wilson, Joan E.;
- Almasy, Laura;
- De Andrade, Mariza;
- Bailey, Julia;
- Bickeböller, Heike;
- Cordell, Heather J.;
- Daw, E. Warwick;
- Goldin, Lynn;
- Goode, Ellen L.;
- Gray-McGuire, Courtney;
- Hening, Wayne;
- Jarvik, Gail;
- Maher, Brion S.;
- Mendell, Nancy;
- Paterson, Andrew D.;
- Rice, John;
- Satten, Glen;
- Suarez, Brian;
- Vieland, Veronica;
- Wilcox, Marsha
Publication type:
Article
Common polymorphism in H19 associated with birthweight and cord blood IGF-II levels in humans.
Published in:
BMC Genetics, 2005, v. 6, p. 1, doi. 10.1186/1471-2156-6-22
By:
- Petry, Clive J;
- Ong, Ken K;
- Barratt, Bryan J;
- Wingate, Diane;
- Cordell, Heather J;
- Ring, Susan M;
- Pembrey, Marcus E;
- Reik, Wolf;
- Todd, John A;
- Dunger, David B
Publication type:
Article
Linkage analysis of a derived glucose phenotype in the Genetic Analysis Workshop 13 simulated data using a variety of Haseman-Elston based regression methods.
Published in:
BMC Genetics, 2003, v. 4, p. S6, doi. 10.1186/1471-2156-4-S1-S6
By:
- Cordell, Heather J.;
- Howson, Joanna M. M.;
- Clayton, David G.
Publication type:
Article
Haplin power analysis: a software module for power and sample size calculations in genetic association analyses of family triads and unrelated controls.
Published in:
BMC Bioinformatics, 2019, v. 20, n. 1, p. 1, doi. 10.1186/s12859-019-2727-3
By:
- Gjerdevik, Miriam;
- Jugessur, Astanand;
- Haaland, Øystein A.;
- Romanowska, Julia;
- Lie, Rolv T.;
- Cordell, Heather J.;
- Gjessing, Håkon K.
Publication type:
Article
Phenotypic heterogeneity in m.3243A>G mitochondrial disease: The role of nuclear factors.
Published in:
Annals of Clinical & Translational Neurology, 2018, v. 5, n. 3, p. 333, doi. 10.1002/acn3.532
By:
- Pickett, Sarah J.;
- Grady, John P.;
- Ng, Yi Shiau;
- Gorman, Gráinne S.;
- Schaefer, Andrew M.;
- Wilson, Ian J.;
- Cordell, Heather J.;
- Turnbull, Doug M.;
- Taylor, Robert W.;
- McFarland, Robert
Publication type:
Article
Genetic variants associated with leaf spot disease resistance in oil palm (Elaeis guineensis): A genome‐wide association study.
Published in:
Plant Pathology, 2023, v. 72, n. 9, p. 1626, doi. 10.1111/ppa.13774
By:
- Wibowo, Cahyo S.;
- Apriyanto, Ardha;
- Ernawan, Reza;
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Nature Communications, 2015, v. 6, n. 9, p. 8019, doi. 10.1038/ncomms9019
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Clinical Genetics, 2023, v. 103, n. 3, p. 330, doi. 10.1111/cge.14251
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BMC Medical Genomics, 2024, v. 17, n. 1, p. 1, doi. 10.1186/s12920-024-01927-2
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