• 8719 Citations
  • 38 h-Index
20022019
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Research Output 2002 2019

2019

Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data

International Inflammatory Bowel Disease Genetics Consortium (IIBDGC), 17 Jul 2019, In : Scientific Reports. 9, 1, 10351.

Research output: Contribution to journalArticle

Open Access
Crohn Disease
Genome
Logistic Models
ROC Curve
Area Under Curve

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases (vol 9, 1864, 2018)

Blue Mountains Eye Study-GWAS Grp, NEIGHBORHOOD Consortium & Wellcome Trust Case Control, 8 Jan 2019, In : Nature Communications. 10, 3 p., 155.

Research output: Contribution to journalArticle

Open Access
2 Citations (Scopus)

Determinants for progression from asymptomatic infection to symptomatic visceral leishmaniasis: A cohort study

Chakravarty, J., Hasker, E., Kansal, S., Singh, O. P., Malaviya, P., Singh, A. K., Chourasia, A., Singh, T., Sudarshan, M., Singh, A. P., Singh, B., Singh, R. P., Ostyn, B., Fakiola, M., Picado, A., Menten, J., Blackwell, J. M., Wilson, M. E., Sacks, D., Boelaert, M. & 1 othersSundar, S., 1 Mar 2019, In : PLoS Neglected Tropical Diseases. 13, 3, p. e0007216

Research output: Contribution to journalArticle

Open Access
Asymptomatic Infections
Visceral Leishmaniasis
Cohort Studies
Leishmania donovani
Enzyme-Linked Immunosorbent Assay

HLA-DR Class II expression on myeloid and lymphoid cells in relation to HLA-DRB1 as a genetic risk factor for visceral leishmaniasis

Singh, B., Fakiola, M., Sudarshan, M., Oommen, J., Singh, S. S., Sundar, S. & Blackwell, J. M., 1 Feb 2019, In : Immunology. 156, 2, p. 174-186 13 p.

Research output: Contribution to journalArticle

HLA-DRB1 Chains
Visceral Leishmaniasis
HLA-DR Antigens
Myeloid Cells
Lymphocytes
1 Citation (Scopus)

Meta-taxonomic analysis of prokaryotic and eukaryotic gut flora in stool samples from visceral leishmaniasis cases and endemic controls in Bihar State India

Lappan, R., Classon, C., Kumar, S., Singh, O. P., De Almeida, R. V., Chakravarty, J., Kumari, P., Kansal, S., Sundar, S. & Blackwell, J. M., 1 Jan 2019, In : PLoS Neglected Tropical Diseases. 13, 9, e0007444.

Research output: Contribution to journalArticle

Open Access
Visceral Leishmaniasis
Blastocystis
Meta-Analysis
India
Escherichia

Personalised analytics for rare disease diagnostics

Anderson, D., Baynam, G., Blackwell, J. M. & Lassmann, T., 1 Dec 2019, In : Nature Communications. 10, 1, 5274.

Research output: Contribution to journalArticle

Open Access
Rare Diseases
phenotype
gene expression
Tissue
Phenotype

Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer (vol 7, 11496, 2017)

Ngo, H. M., Zhou, Y., Lorenzi, H., Wang, K., Kim, T-K., Zhou, Y., El Bissati, K., Mui, E., Fraczek, L., Rajagopala, S. V., Roberts, C. W., Henriquez, F. L., Montpetit, A., Blackwell, J. M., Jamieson, S. E., Wheeler, K., Begeman, I. J., Naranjo-Galvis, C., Alliey-Rodriguez, N., Davis, R. G. & 12 othersSoroceanu, L., Cobbs, C., Steindler, D. A., Boyer, K., Noble, A. G., Swisher, C. N., Heydemann, P. T., Rabiah, P., Withers, S., Soteropoulos, P., Hood, L. & McLeod, R., 28 May 2019, In : Scientific Reports. 9, 1 p., 8110.

Research output: Contribution to journalArticle

Open Access

Transcriptional blood signatures for active and amphotericin B treated visceral leishmaniasis in India

Fakiola, M., Singh, O. P., Syn, G., Singh, T., Singh, B., Chakravarty, J., Sundar, S. & Blackwell, J. M., 16 Aug 2019, In : PLoS Neglected Tropical Diseases. 13, 8, p. e0007673

Research output: Contribution to journalArticle

Open Access
Visceral Leishmaniasis
Amphotericin B
India
Genes
Gene Expression

Transketolase and vitamin B1 influence on ROS-dependent neutrophil extracellular traps (NETs) formation

Riyapa, D., Rinchai, D., Muangsombut, V., Wuttinontananchai, C., Toufiq, M., Chaussabel, D., Ato, M., Blackwell, J. M. & Korbsrisate, S., 15 Aug 2019, In : PLoS One. 14, 8, e0221016.

Research output: Contribution to journalArticle

Open Access
Transketolase
transketolase
Thiamine
thiamin
neutrophils
2018
1 Citation (Scopus)
Open Access
Toxoplasma
Proteome
Cell Nucleus
Epigenomics
Computer Simulation

Arylsulphatase A Pseudodeficiency (ARSA-PD), hypertension and chronic renal disease in Aboriginal Australians

Tang, D., Fakiola, M., Syn, G., Anderson, D., Cordell, H. J., Scaman, E. S. H., Davis, E., Miles, S. J., McLeay, T., Jamieson, S. E., Lassmann, T. & Blackwell, J. M., 1 Dec 2018, In : Scientific Reports. 8, 1, 10912.

Research output: Contribution to journalArticle

Open Access
Cerebroside-Sulfatase
Chronic Renal Insufficiency
Type 2 Diabetes Mellitus
Chylomicrons
Hypertension
7 Citations (Scopus)

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

Iglesias, A. I., Mishra, A., Vitart, V., Bykhovskaya, Y., Höhn, R., Springelkamp, H., Cuellar-Partida, G., Gharahkhani, P., Bailey, J. N. C., Willoughby, C. E., Li, X., Yazar, S., Nag, A., Khawaja, A. P., Polašek, O., Siscovick, D., Mitchell, P., Tham, Y. C., Haines, J. L., Kearns, L. S. & 124 othersHayward, C., Shi, Y., Van Leeuwen, E. M., Taylor, K. D., Wang, J. J., Rochtchina, E., Attia, J., Scott, R., Holliday, E. G., Baird, P. N., Xie, J., Inouye, M., Viswanathan, A., Sim, X., Bonnemaijer, P., Rotter, J. I., Martin, N. G., Zeller, T., Mills, R. A., Staffieri, S. E., Jonas, J. B., Schmidtmann, I., Boutin, T., Kang, J. H., Lucas, S. E. M., Wong, T. Y., Beutel, M. E., Wilson, J. F., Allingham, R. R., Brilliant, M. H., Budenz, D. L., Christen, W. G., Fingert, J., Friedman, D. S., Gaasterland, D., Gaasterland, T., Hauser, M. A., Kraft, P., Lee, R. K., Lichter, P. R., Liu, Y., Loomis, S. J., Moroi, S. E., Pericak-Vance, M. A., Realini, A., Richards, J. E., Schuman, J. S., Scott, W. K., Singh, K., Sit, A. J., Vollrath, D., Weinreb, R. N., Wollstein, G., Zack, D. J., Zhang, K., Donnelly, P., Barroso, I., Blackwell, J. M., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Wood, N. W., Spencer, C. C. A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R., Strange, A., Su, Z., Vukcevic, D., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., McCann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P., Uitterlinden, A. G., Vithana, E. N., Foster, P. J., Hysi, P. G., Hewitt, A. W., Khor, C. C., Pasquale, L. R., Montgomery, G. W., Klaver, C. C. W., Aung, T., Pfeiffer, N., MacKey, D. A., Hammond, C. J., Cheng, C. Y., Craig, J. E., Rabinowitz, Y. S., Wiggs, J. L., Burdon, K. P., Van Duijn, C. M. & MacGregor, S., 1 Dec 2018, In : Nature Communications. 9, 1, 1864.

Research output: Contribution to journalArticle

Open Access
eye diseases
Eye Diseases
genome
Genome-Wide Association Study
Keratoconus
3 Citations (Scopus)
toxoplasmosis
Toxoplasmosis
Toxoplasma
amyloid
dopamine
2 Citations (Scopus)

Epitope-binding characteristics for risk versus protective DRB1 alleles for visceral leishmaniasis

Singh, T., Fakiola, M., Oommen, J., Singh, A. P., Singh, A. K., Smith, N., Chakravarty, J., Sundar, S. & Blackwell, J. M., 15 Apr 2018, In : Journal of Immunology. 200, 8, p. 2727-2737 11 p.

Research output: Contribution to journalArticle

Open Access
Visceral Leishmaniasis
Epitopes
Alleles
HLA-DRB1 Chains
Peptides
2017
3 Citations (Scopus)

Analysis of expression of FLI1 and MMP1 in American cutaneous leishmaniasis caused by Leishmania braziliensis infection

Almeida, L., Silva, J. A., Andrade, V. M., Machado, P., Jamieson, S. E., Carvalho, E. M., Blackwell, J. M. & Castellucci, L. C., 1 Apr 2017, In : Infection, Genetics and Evolution. 49, p. 212-220 9 p.

Research output: Contribution to journalArticle

Leishmania braziliensis
leishmaniasis
Friend murine leukemia virus
Virus Integration
interstitial collagenase
2 Citations (Scopus)

Burkholderia pseudomallei Evades Nramp1 (Sic11a1)- and NADPH Oxidase-Mediated Killing in Macrophages and Exhibits in Nramp1-Dependent Virulence Gene Expression

Muangsombut, V., Withatanung, P., Srinon, V., Chantratita, N., Stevens, M. P., Blackwell, J. M. & Korbsrisate, S., 8 Aug 2017, In : Frontiers in Cellular and Infection Microbiology. 7, 13 p., 350.

Research output: Contribution to journalArticle

Open Access
4 Citations (Scopus)

Comparative analyses of whole genome sequences of Leishmania infantum isolates from humans and dogs in northeastern Brazil

Teixeira, D. G., Monteiro, G. R. G., Martins, D. R. A., Fernandes, M. Z., Macedo-Silva, V., Ansaldi, M., Nascimento, P. R. P., Kurtz, M. A., Streit, J. A., Ximenes, M. F. F. M., Pearson, R. D., Miles, A., Blackwell, J. M., Wilson, M. E., Kitchen, A., Donelson, J. E., Lima, J. P. M. S. & Jeronimo, S. M. B., 1 Sep 2017, In : International Journal for Parasitology. 47, 10-11, p. 655-665 11 p.

Research output: Contribution to journalArticle

Open Access
Leishmania infantum
Brazil
Chromosomes
Genome
Dogs
2 Citations (Scopus)

Comprehensive candidate gene analysis for symptomatic or asymptomatic outcomes of Leishmania infantum infection in Brazil

Weirather, J. L., Duggal, P., Nascimento, E. L., Monteiro, G. R., Martins, D. R., Lacerda, H. G., Fakiola, M., Blackwell, J. M., Jeronimo, S. M. B. & Wilson, M. E., 1 Jan 2017, In : Annals of Human Genetics. 81, 1, p. 41-48 8 p.

Research output: Contribution to journalArticle

Leishmania infantum
Visceral Leishmaniasis
Delayed Hypersensitivity
Genetic Association Studies
Single Nucleotide Polymorphism
5 Citations (Scopus)

Expression profiling of Sudanese visceral leishmaniasis patients pre- and post-treatment with sodium stibogluconate

Salih, M. A. M., Fakiola, M., Lyons, P. A., Younis, B. M., Musa, A. M., Elhassan, A. M., Anderson, D., Syn, G., Ibrahim, M. E., Blackwell, J. M. & Mohamed, H. S., 1 Jun 2017, In : Parasite Immunology. 39, 6, e12431.

Research output: Contribution to journalArticle

Antimony Sodium Gluconate
Visceral Leishmaniasis
Leishmaniasis
Therapeutics
NFATC Transcription Factors
12 Citations (Scopus)

Genome-Wide Analysis of Genetic Risk Factors for Rheumatic Heart Disease in Aboriginal Australians Provides Support for Pathogenic Molecular Mimicry

Gray, L. A., D'Antoine, H. A., Tong, S. Y. C., McKinnon, M., Bessarab, D., Brown, N., Reményi, B., Steer, A., Syn, G., Blackwell, J. M., Inouye, M. & Carapetis, J. R., 12 Dec 2017, In : The Journal of infectious diseases. 216, 11, p. 1460-1470 11 p.

Research output: Contribution to journalArticle

Molecular Mimicry
Rheumatic Heart Disease
HLA Antigens
Genome
Streptococcus
5 Citations (Scopus)
Open Access
17 Citations (Scopus)

Toxoplasma Modulates Signature Pathways of Human Epilepsy, Neurodegeneration & Cancer

Ngô, H. M., Zhou, Y., Lorenzi, H., Wang, K., Kim, T. K., Zhou, Y., Bissati, K. E., Mui, E., Fraczek, L., Rajagopala, S. V., Roberts, C. W., Henriquez, F. L., Montpetit, A., Blackwell, J. M., Jamieson, S. E., Wheeler, K., Begeman, I. J., Naranjo-Galvis, C., Alliey-Rodriguez, N., Davis, R. G. & 12 othersSoroceanu, L., Cobbs, C., Steindler, D. A., Boyer, K., Noble, A. G., Swisher, C. N., Heydemann, P. T., Rabiah, P., Withers, S., Soteropoulos, P., Hood, L. & McLeod, R., 1 Dec 2017, In : Scientific Reports. 7, 1, 11496.

Research output: Contribution to journalArticle

Open Access
Toxoplasma
Epilepsy
Brain
Neoplasms
Congenital Toxoplasmosis
2016
2 Citations (Scopus)

Candidate gene analysis supports a role for polymorphisms at TCF7L2 as risk factors for type 2 diabetes in Sudan

Ibrahim, A. T., Hussain, A., Salih, M. A. M., Ibrahim, O. A., Jamieson, S. E., Ibrahim, M. E., Blackwell, J. M. & Mohamed, H. S., 2016, In : Journal of Diabetes and Metabolic Disorders. 15, 1, p. 4 4 p.

Research output: Contribution to journalArticle

Open Access
Sudan
Genetic Association Studies
Type 2 Diabetes Mellitus
Single Nucleotide Polymorphism
Odds Ratio

Epigenetics in Infectious diseases

Syn, W. F., Blackwell, J. & Jamieson, S., 2016, Epigenetic Biomarkers and Diagnostics. G-G. JL. (ed.). London, UK: Academic Press, p. 377-400 24 p. (Translational epigenetics series).

Research output: Chapter in Book/Conference paperChapter

2 Citations (Scopus)

Fine mapping under linkage peaks for symptomatic or asymptomatic outcomes of Leishmania infantum infection in Brazil

Weirather, J. L., Duggal, P., Nascimento, E. L., Monteiro, G. R., Martins, D. R., Lacerda, H. G., Fakiola, M., Blackwell, J., Jeronimo, S. M. B. & Wilson, M. E., 2016, In : Infection, Genetics and Evolution. 43, p. 1-5

Research output: Contribution to journalArticle

Leishmania infantum
Chromosome Mapping
visceral leishmaniasis
leishmaniasis
Single Nucleotide Polymorphism

Immunogenetics of Parasitic and Bacterial Disease

Blackwell, J., 2016, Encyclopedia of Immunobiology: immunity to pathogens and tumors. Biron, C., Finn, O. & Kaye, P. (eds.). United Kingdom: Academic Press, Vol. 4. p. 7-15 9 p.

Research output: Chapter in Book/Conference paperChapter

14 Citations (Scopus)

Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children

Rautanen, A., Pirinen, M., Mills, T. C., Rockett, K. A., Strange, A., Ndungu, A. W., Naranbhai, V., Gilchrist, J. J., Bellenguez, C., Freeman, C., Band, G., Bumpstead, S. J., Edkins, S., Giannoulatou, E., Gray, E., Dronov, S., Hunt, S. E., Langford, C., Pearson, R. D., Su, Z. & 37 othersVukcevic, D., Macharia, A. W., Uyoga, S., Ndila, C., Mturi, N., Njuguna, P., Mohammed, S., Berkley, J. A., Mwangi, I., Mwarumba, S., Kitsao, B. S., Lowe, B. S., Morpeth, S. C., Khandwalla, I., Blackwell, J., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Deloukas, P., Peltonen, L., Williams, T. N., Scott, J. A. G., Chapman, S. J., Donnelly, P., Hill, A. V. S. & Spencer, C. C. A., 2016, In : American Journal of Human Genetics. 98, 6, p. 1092-1100

Research output: Contribution to journalArticle

Open Access
Long Noncoding RNA
Bacteremia
Africa South of the Sahara
Kenya
Genome-Wide Association Study
12 Citations (Scopus)

Reference genotype and exome data from an Australian Aboriginal population for health-based research

Tang, D., Anderson, D., Francis, R., Syn, G., Jamieson, S., Lassmann, T. & Blackwell, J., 12 Apr 2016, In : Scientific Data. 3, p. 1-7 7 p., 160023.

Research output: Contribution to journalArticle

Open Access
Nucleotides
Genotype
Sequencing
Health
Genomics
3 Citations (Scopus)

The -308 bp TNF gene polymorphism influences tumor necrosis factor expression in leprosy patients in Bahia State, Brazil

Oliveira, J. M., Rêgo, J. L., De Lima Santana, N., Braz, M., Jamieson, S., Vieira, T. S., Magalhães, T. L., Machado, P. R. L., Blackwell, J. & Castellucci, L. C., 2016, In : Infection, Genetics and Evolution. 39, p. 147-154

Research output: Contribution to journalArticle

leprosy
tumor necrosis factors
Leprosy
tumor
Brazil
22 Citations (Scopus)

The rare and undiagnosed diseases diagnostic service - application of massively parallel sequencing in a state-wide clinical service

Baynam, G., Pachter, N., McKenzie, F., Townshend, S., Slee, J., Kiraly-Borri, C., Vasudevan, A., Hawkins, A., Broley, S., Schofield, L., Verhoef, H., Walker, C. E. E., Molster, C., Blackwell, J. M., Jamieson, S., Tang, D., Lassmann, T., Mina, K., Beilby, J., Davis, M. & 5 othersLaing, N., Murphy, L., Weeramanthri, T., Dawkins, H. & Goldblatt, J., 2016, In : Orphanet Journal of Rare Diseases. 11, 7 p., 77.

Research output: Contribution to journalArticle

Genetic Services
Diagnostic Services
High-Throughput Nucleotide Sequencing
Rare Diseases
Western Australia
2 Citations (Scopus)

Translating aboriginal genomics — four letters closing the gap

Baynam, G. S., Pearson, G. & Blackwell, J., 17 Oct 2016, In : Medical Journal of Australia. 205, 8, p. 379-379.e1 1 p.

Research output: Contribution to journalLetter

2015
19 Citations (Scopus)
137 Downloads (Pure)

First genome-wide association study in an Australian Aboriginal population provides insights into genetic risk factors for body mass index and type 2 diabetes

Anderson, D., Cordell, H. J., Fakiola, M., Francis, R. W., Syn, G., Scaman, E. S. H., Davis, E., Miles, S. J., Mcleay, T., Jamieson, S. & Blackwell, J., 2015, In : PLoS One. 10, 3, p. 1-25

Research output: Contribution to journalArticle

Open Access
File
Genome-Wide Association Study
Medical problems
noninsulin-dependent diabetes mellitus
Type 2 Diabetes Mellitus
body mass index

Genome-wide association study of IgG1 responses to the choline-binding protein PspC of Streptococcus pneumoniae

Anderson, D., Fakiola, M., Hales, B., Pennell, C., Thomas, W. & Blackwell, J., Jul 2015, In : Genes and Immunity. 16, 5, p. 289-296 8 p.

Research output: Contribution to journalArticle

Genome-Wide Association Study
HLA Antigens
Choline
Streptococcus pneumoniae
Protein C
1 Citation (Scopus)

Wound healing genes and susceptibility to cutaneous leishmaniasis in Brazil: Role of COL1A1

Almeida, L. M., Oliveira, J. V. A., Guimarães, L. H., Carvalho, E. M. R. D., Blackwell, J. & Castellucci, L. C., 2015, In : Infection, Genetics and Evolution. 30, p. 225-229

Research output: Contribution to journalArticle

leishmaniasis
cutaneous leishmaniasis
Cutaneous Leishmaniasis
tissue repair
Leishmaniasis
2014
27 Citations (Scopus)

A Genome-wide Association Analysis of a Broad Psychosis Phenotype Identifies Three Loci for Further Investigation

Bramon, E., Pirinen, M., Strange, A., Lin, K., Freeman, C., Bellenguez, C., Su, Z., Band, G., Pearson, R., Vukcevic, D., Langford, C., Deloukas, P., Hunt, S., Gray, E., Dronov, S., Potter, S. C., Tashakkori-Ghanbaria, A., Edkins, S., Bumpstead, S. J., Arranz, M. J. & 79 othersBakker, S., Bender, S., Bruggeman, R., Cahn, W., Chandler, D., Collier, D. A., Crespo-Facorro, B., Dazzan, P., De Haan, L., Di Forti, M., Dragovic, M., Giegling, I., Hall, J., Iyegbe, C., Jablensky, A., Kahn, R. S., Kalaydjieva, L., Kravariti, E., Lawrie, S., Linszen, D. H., Mata, I., Mcdonald, C., Mcintosh, A., Myin-Germeys, I., Ophoff, R. A., Pariante, C. M., Paunio, T., Picchioni, M., Ripke, S., Rujescu, D., Sauer, H., Shaikh, M., Sussmann, J., Suvisaari, J., Tosato, S., Toulopoulou, T., Van Os, J., Walshe, M., Weisbrod, M., Whalley, H., Wiersma, D., Blackwell, J., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J. A. Z., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Wood, N., Barrosso, I., Peltonen, L., Lewis, C. M., Murray, R. M., Donnelly, P., Powell, J., Spencer, C., Viswanathan, A. C., Hellenthal, G., Giannoulatou, E., Gwilliam, R., Blackburn, H., Gillman, M., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Ravindrarajah, R., Ricketts, M., Waller, M., Weston, P., Widaa, S., Whittaker, P. & Mccarthy, M. I., 2014, In : Biological Psychiatry. 75, 5, p. 386-397 12 p.

Research output: Contribution to journalArticle

51 Citations (Scopus)

Comparison of Methods to Account for Relatedness in Genome-Wide Association Studies with Family-Based Data

Eu-Ahsunthornwattana, J., Miller, E. N., Fakiola, M., Jeronimo, S. M. B., Blackwell, J. & Cordell, H. J., 2014, In : PLoS Genetics. 10, 7, p. e1004445

Research output: Contribution to journalArticle

Open Access
3 Citations (Scopus)

Examining ERBB2 as a candidate gene for susceptibility to leprosy (Hansen's disease) in Brazil

Araújo, S. R. F., Jamieson, S., Dupnik, K. M., Monteiro, G. R., Nobre, M. L., Dias, M. S., Neto, P. B. T., Queiroz, M. C. P., Gomes, C. E. M., Blackwell, J. & Jeronimo, S. M. B., 2014, In : Memorias do Instituto Oswaldo Cruz. 109, 2, p. 7pp

Research output: Contribution to journalArticle

Open Access
5 Citations (Scopus)

Genetic and functional evidence for a locus controlling otitis media at chromosome 10q26.3

Rye, M., Scaman, E. S. H., Thornton, R., Vijayasekaran, S., Coates, H., Francis, R., Pennell, C., Blackwell, J. & Jamieson, S., 2014, In : BMC Medical Genetics. 15, 1, 18 p.

Research output: Contribution to journalArticle

Open Access
Otitis Media
Chromosomes
Single Nucleotide Polymorphism
Adenoids
Otitis Media with Effusion
26 Citations (Scopus)
Genome-Wide Association Study
Vitamin D
Cohort Studies
Chromosomes
Pregnancy
23 Citations (Scopus)

Host genetic factors in American cutaneous leishmaniasis: A critical appraisal of studies conducted in an endemic area of Brazil

Castellucci, L. C., De Almeida, L. F., Jamieson, S., Fakiola, M., De Carvalho, E. M. & Blackwell, J., 2014, In : Memorias do Instituto Oswaldo Cruz. 109, 3, p. 279-288

Research output: Contribution to journalArticle

Open Access
Cutaneous Leishmaniasis
Brazil
Genes
Leishmania braziliensis
Disease Vectors
3 Citations (Scopus)

Insights into the possible role of IFNG and IFNGR1 in Kala-azar and Post Kala-azar Dermal Leishmaniasis in Sudanese patients

Salih, M. A., Fakiola, M., Abdelraheem, M. H., Younis, B. M., Musa, A. M., Elhassan, A. M., Blackwell, J., Ibrahim, M. E. & Mohamed, H. S., 2014, In : BMC Infectious Diseases. 41, 1, p. 662

Research output: Contribution to journalArticle

Open Access
42 Citations (Scopus)

The correlation between reading and mathematics ability at age twelve has a substantial genetic component

Davis, O. S. P., Band, G., Pirinen, M., Haworth, C. M. A., Meaburn, E. L., Kovas, Y., Harlaar, N., Docherty, S. J., Hanscombe, K. B., Trzaskowski, M., Curtis, C. J. C., Strange, A., Freeman, C., Bellenguez, C., Su, Z., Pearson, R., Vukcevic, D., Langford, C., Deloukas, P., Hunt, S. & 32 othersGray, E., Dronov, S., Potter, S. C., Tashakkori-Ghanbaria, A., Edkins, S., Bumpstead, S. J., Blackwell, J., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J. A. Z., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Barroso, I., Peltonen, L., Dale, P. S., Petrill, S. A., Schalkwyk, L. S., Craig, I. W., Lewis, C. M., Price, T. S., Donnelly, P., Plomin, R. & Spencer, C. C. A., 2014, In : Nature Communications. 5, p. 4204

Research output: Contribution to journalArticle

Open Access
2013
22 Citations (Scopus)

A "Candidate-Interactome" Aggregate Analysis of Genome-Wide Association Data in Multiple Sclerosis

Mechelli, R., Umeton, R., Policano, C., Annibali, V., Coarelli, G., Ricigliano, V. A. G., Vittori, D., Fornasiero, A., Buscarinu, M. C., Sawcer, S., Hellenthal, G., Pirinen, M., Spencer, C. C. A., Patsopoulos, N. A., Moutsianas, L., Dilthey, A., Su, Z., Freeman, C., Hunt, S. E., Edkins, S. & 233 othersGray, E., Booth, D. R., Potter, S. C., Goris, A., Band, G., Oturai, A. B., Strange, A., Saarela, J., Bellenguez, C., Fontaine, B., Gillman, M., Hemmer, B., Gwilliam, R., Zipp, F., Jayakumar, A., Martin, R., Leslie, S., Hawkins, S., Giannoulatou, E., D'Alfonso, S., Blackburn, H., Boneschi, F. M., Liddle, J., Harbo, H. F., Perez, M. L., Spurkland, A., Waller, M. J., Mycko, M. P., Ricketts, M., Comabella, M., Hammond, N., Kockum, I., Mccann, O. T., Ban, M., Whittaker, P., Kemppinen, A., Weston, P., Hawkins, C., Widaa, S., Zajicek, J., Dronov, S., Robertson, N., Bumpstead, S. J., Barcellos, L. F., Ravindrarajah, R., Abraham, R., Alfredsson, L., Ardlie, K., Aubin, C., Baker, A., Baker, K., Baranzini, S. E., Bergamaschi, L., Bergamaschi, R., Bernstein, A., Berthele, A., Boggild, M., Bradfield, J. P., Brassat, D., Broadley, S. A., Buck, D., Butzkueven, H., Capra, R., Carroll, W. M., Cavalla, P., Celius, E. G., Cepok, S., Chiavacci, R., Clerget-Darpoux, F., Clysters, K., Comi, G., Cossburn, M., Cournu-Rebeix, I., Cox, M. B., Cozen, W., Cree, B. A. C., Cross, A. H., Cusi, D., Daly, M. J., Davis, E., De Bakker, P. I. W., Debouverie, M., D'Hooghe, M. B., Dixon, K., Dobosi, R., Dubois, B., Ellinghaus, D., Elovaara, I., Esposito, F., Fontenille, C., Foote, S., Franke, A., Galimberti, D., Ghezzi, A., Glessner, J., Gomez, R., Gout, O., Graham, C., Grant, S. F. A., Guerini, F. R., Hakonarson, H., Hall, P., Hamsten, A., Hartung, H-P., Heard, R. N., Heath, S., Hobart, J., Hoshi, M., Infante-Duarte, C., Ingram, G., Ingram, W., Islam, T., Jagodic, M., Kabesch, M., Kermode, A., Kilpatrick, T. J., Kim, C., Klopp, N., Koivisto, K., Larsson, M., Lathrop, M., Lechner-Scott, J. S., Leone, M. A., Leppä, V., Liljedahl, U., Bomfim, I. L., Lincoln, R. R., Link, J., Liu, J., Lorentzen, Å. R., Lupoli, S., Macciardi, F., Mack, T., Marriott, M., Martinelli, V., Mason, D., Mccauley, J. L., Mentch, F., Mero, I-L., Mihalova, T., Montalban, X., Mottershead, J., Myhr, K-M., Naldi, P., Ollier, W., Page, A., Palotie, A., Pelletier, J., Piccio, L., Pickersgill, T., Piehl, F., Pobywajlo, S., Quach, H. L., Ramsay, P. P., Reunanen, M., Reynolds, R., Rioux, J. D., Rodegher, M., Roesner, S., Rubio, J. P., Rückert, I-M., Salvi, E., Santaniello, A., Schaefer, C. A., Schreiber, S., Schulze, C., Scott, R. J., Sellebjerg, F., Selmaj, K. W., Sexton, D., Shen, L., Simms-Acuna, B., Skidmore, S., Sleiman, P. M. A., Smestad, C., Sørensen, P. S., Søndergaard, H. B., Stankovich, J., Strange, R. C., Sulonen, A-M., Sundqvist, E., Syvänen, A-C., Taddeo, F., Taylor, B., Blackwell, J., Tienari, P., Bramon, E., Tourbah, A., Brown, M. A., Tronczynska, E., Casas, J. P., Tubridy, N., Corvin, A., Vickery, J., Jankowski, J., Villoslada, P., Markus, H. S., Wang, K., Mathew, C. G., Wason, J., Palmer, C. N. A., Wichmann, H-E., Plomin, R., Willoughby, E., Rautanen, A., Winkelmann, J., Wittig, M., Trembath, R. C., Yaouanq, J., Viswanathan, A. C., Zhang, H., Wood, N. W., Zuvich, R., Deloukas, P., Langford, C., Duncanson, A., Oksenberg, J. R., Pericak-Vance, M. A., Haines, J. L., Olsson, T., Hillert, J., Ivinson, A. J., De Jager, P. L., Peltonen, L., Stewart, G. J., Hafler, D. A., Hauser, S. L., Mcvean, G., Donnelly, P., Compston, A., Romano, S., Salvetti, M. & Ristori, G., 2013, In : PLoS One. 8, 5, p. 9pp

Research output: Contribution to journalArticle

Open Access
18 Citations (Scopus)

A Genome-Wide Search for Type 2 Diabetes Susceptibility Genes in an Extended Arab Family

Al Safar, H. S., Cordell, H. J., Jafer, O., Anderson, D., Jamieson, S., Fakiola, M., Khazanehdari, K., Tay, G. & Blackwell, J., 2013, In : Annals of Human Genetics. 77, 6, p. 488-503

Research output: Contribution to journalArticle

30 Citations (Scopus)

Association of a NOD2 gene polymorphism and T-helper 17 cells with presumed ocular toxoplasmosis

Dutra, M. S., Béla, S. R., Peixoto-Rangel, A. L., Fakiola, M., Cruz, A. G., Gazzinelli, A., Quites, H. F., Bahia-Oliveira, L. M. G., Peixe, R. G., Campos, W. R., Higino-Rocha, A. C., Miller, N. E., Blackwell, J., Antonelli, L. R. & Gazzinelli, R. T., 2013, In : Journal of Infectious Diseases. 207, 1, p. 152-163

Research output: Contribution to journalArticle

65 Citations (Scopus)

Common variants in the HLA-DRB1-HLA-DQA1 HLA class II region are associated with susceptibility to visceral leishmaniasis

Fakiola, M., Strange, A., Cordell, H. J., Miller, E. N., Pirinen, M., Su, Z., Mishra, A., Mehrotra, S., Monteiro, G. R., Band, G., Bellenguez, C., Dronov, S., Edkins, S., Freeman, C., Giannoulatou, E., Gray, E., Hunt, S. E., Lacerda, H. G., Langford, C., Pearson, R. & 31 othersPontes, N. N., Rai, M., Singh, S. P., Smith, L., Sousa, O., Vukcevic, D., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Wilson, M. E., Deloukas, P., Peltonen, L., Christiansen, F., Witt, C., Jeronimo, S. M. B., Sundar, S., Spencer, C. C. A., Blackwell, J. & Donnelly, P., 2013, In : Nature Genetics. 45, 2, p. 208-213

Research output: Contribution to journalArticle

5 Citations (Scopus)
865 Citations (Scopus)

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

Ripke, S., O'Dushlaine, C., Chambert, K., Moran, J. L., Kähler, A. K., Akterin, S., Bergen, S. E., Collins, A. L., Crowley, J. J., Fromer, M., Kim, Y., Lee, S. H., Magnusson, P. K. E., Sanchez, N., Stahl, E. A., Williams, S., Wray, N. R., Xia, K., Bettella, F., Borglum, A. D. & 147 othersBulik-Sullivan, B. K., Cormican, P., Craddock, N., De Leeuw, C., Durmishi, N., Gill, M., Golimbet, V., Hamshere, M. L., Holmans, P., Hougaard, D. M., Kendler, K. S., Lin, K., Morris, D. W., Mors, O., Mortensen, P. B., Neale, B. M., O'Neill, F. A., Owen, M. J., Milovancevic, M. P., Posthuma, D., Powell, J., Richards, A. L., Riley, B. P., Ruderfer, D., Rujescu, D., Sigurdsson, E., Silagadze, T., Smit, A. B., Stefansson, H., Steinberg, S., Suvisaari, J., Tosato, S., Verhage, M., Walters, J. T., Levinson, D. F., Gejman, P. V., Laurent, C., Mowry, B. J., O'Donovan, M. C., Pulver, A. E., Schwab, S., Wildenauer, D., Dudbridge, F., Shi, J., Albus, M., Alexander, M., Campion, D., Cohen, D., Dikeos, D., Duan, J., Eichhammer, P., Godard, S., Hansen, M., Lerer, F. B., Liang, K-Y., Maier, W., Mallet, J., Nertney, D. A., Nestadt, G., Norton, N., Papadimitriou, G. N., Ribble, R., Sanders, A. R., Silverman, J. M., Walsh, D., Williams, N. M., Wormley, B., Arranz, M. J., Bakker, S., Bender, S., Bramon, E., Collier, D., Crespo-Facorro, B., Hall, J., Iyegbe, C., Jablensky, A., Kahn, R. S., Kalaydjieva, L., Lawrie, S., Lewis, C. M., Linszen, D. H., Mata, I., Mcintosh, A., Murray, R. M., Ophoff, R. A., Van Os, J., Walshe, M., Weisbrod, M., Wiersma, D., Donnelly, P., Barroso, I., Blackwell, J., Brown, M. A., Casas, J. P., Corvin, A. P., Deloukas, P., Duncanson, A., Jankowski, J., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N. W., Spencer, C. C. A., Band, G., Bellenguez, C., Freeman, C., Hellenthal, G., Giannoulatou, E., Pirinen, M., Pearson, R. D., Strange, A., Su, Z., Vukcevic, D., Langford, C., Hunt, S. E., Edkins, S., Gwilliam, R., Blackburn, H., Bumpstead, S. J., Dronov, S., Gillman, M., Gray, E., Hammond, N., Jayakumar, A., Mccann, O. T., Liddle, J., Potter, S. C., Ravindrarajah, R., Ricketts, M., Tashakkori-Ghanbaria, A., Waller, M. J., Weston, P., Widaa, S., Whittaker, P., Mccarthy, M. I., Stefansson, K., Scolnick, E., Purcell, S., Mccarroll, S. A., Sklar, P., Hultman, C. M. & Sullivan, P. F., 2013, In : Nature Genetics. 45, p. 1150-1159

Research output: Contribution to journalArticle

20 Citations (Scopus)

Genome-wide association study of intraocular pressure identifies the GLCCI1/ICA1 region as a glaucoma susceptibility locus

Strange, A., Bellenguez, C., Sim, X., Luben, R., Hysi, P. G., Ramdas, W. D., Van Koolwijk, L. M. E., Freeman, C., Pirinen, M., Su, Z., Band, G., Pearson, R., Vukcevic, D., Langford, C., Deloukas, P., Hunt, S., Gray, E., Dronov, S., Potter, S. C., Tashakkori-Ghanbaria, A. & 36 othersEdkins, S., Bumpstead, S. J., Blackwell, J., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Jankowski, J. A. Z., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Wood, N. W., Barroso, I., Peltonen, L., Healey, P., Mcguffin, P., Topouzis, F., Klaver, C. C. W., Van Duijn, C. M., Mackey, D., Young, T. L., Hammond, C. J., Khaw, K-T., Wareham, N., Wang, J. J., Wong, T. Y., Foster, P. J., Mitchell, P., Spencer, C. C. A., Donnelly, P. & Viswanathan, A. C., 2013, In : Human Molecular Genetics. 22, 22, p. 4653-4660

Research output: Contribution to journalArticle

Open Access
2012
115 Citations (Scopus)

Common variants at the MHC locus and at chromosome 16q24.1 predispose to Barrett's esophagus

Su, Z., Gay, L. J., Strange, A., Palles, C., Band, G., Whiteman, D. C., Lescai, F., Langford, C., Nanji, M., Edkins, S., Van Der Winkel, A., Levine, D., Sasieni, P., Bellenguez, C., Howarth, K., Freeman, C., Trudgill, N., Tucker, A. T., Pirinen, M., Peppelenbosch, M. P. & 124 othersVan Der Laan, L. J. W., Kuipers, E. J., Drenth, J. P. H., Peters, W. H., Reynolds, J. V., Kelleher, D. P., Mcmanus, R., Grabsch, H., Prenen, H., Bisschops, R., Krishnadath, K., Siersema, P. D., Van Baal, J. W. P. M., Middleton, M., Petty, R., Gillies, R., Burch, N., Bhandari, P., Paterson, S., Edwards, C., Penman, I., Vaidya, K., Ang, Y., Murray, I., Patel, P., Ye, W., Mullins, P., Wu, A. H., Bird, N. C., Dallal, H., Shaheen, N. J., Murray, L. J., Koss, K., Bernstein, L., Romero, Y., Hardie, L. J., Zhang, R., Winter, H., Corley, D. A., Panter, S., Risch, H. A., Reid, B. J., Sargeant, I., Gammon, M. D., Smart, H., Dhar, A., Mcmurtry, H., Ali, H., Liu, G., Casson, A. G., Chow, W-H., Rutter, M., Tawil, A., Morris, D., Nwokolo, C., Isaacs, P., Rodgers, C., Ragunath, K., Macdonald, C., Haigh, C., Monk, D., Davies, G., Wajed, S., Johnston, D., Gibbons, M., Cullen, S., Church, N., Langley, R., Griffin, M., Alderson, D., Deloukas, P., Hunt, S. E., Gray, E., Dronov, S., Potter, S. C., Tashakkori-Ghanbaria, A., Anderson, M., Brooks, C., Blackwell, J., Bramon, E., Brown, M. A., Casas, J. P., Corvin, A., Duncanson, A., Markus, H. S., Mathew, C. G., Palmer, C. N. A., Plomin, R., Rautanen, A., Sawcer, S. J., Trembath, R. C., Viswanathan, A. C., Wood, N., Trynka, G., Wijmenga, C., Cazier, J-B., Atherfold, P., Nicholson, A. M., Gellatly, N. L., Glancy, D., Cooper, S. C., Cunningham, D., Lind, T., Hapeshi, J., Ferry, D., Rathbone, B., Brown, J., Love, S., Attwood, S., Macgregor, S., Watson, P., Sanders, S., Ek, W., Harrison, R. F., Moayyedi, P., De Caestecker, J., Barr, H., Stupka, E., Vaughan, T. L., Peltonen, L., Spencer, C. C. A., Tomlinson, I., Donnelly, P. & Jankowski, J. A. Z., 1 Oct 2012, In : Nature Genetics. 44, 10, p. 1131-1136

Research output: Contribution to journalArticle

Barrett Esophagus
Chromosomes
Odds Ratio
Confidence Intervals
Hiatal Hernia