• 2581 Citations
  • 27 h-Index
20062020
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Research Output 2006 2019

2019

Analysis of the Epigenome in Multiplex Pre-eclampsia Families Identifies SORD, DGKI, and ICA1 as Novel Candidate Risk Genes

Ariff, A., Melton, P. E., Brennecke, S. P. & Moses, E. K., 19 Mar 2019, In : Frontiers in Genetics. 10, 11 p., 227.

Research output: Contribution to journalArticle

Open Access

GENOME-WIDE ASSOCIATION META-ANALYSIS OF AUTISTIC TRAITS IN THE GENERAL POPULATION

Bralten, J., Cadby, G., Jones, R., Whitehouse, A., Moses, E., Shumskaya, E., Buitelaar, J., Franke, B. & Poelmans, G., 2019, In : European Neuropsychopharmacology. 29, p. S754-S754 1 p.

Research output: Contribution to journalAbstract/Meeting Abstract

Identification of novel sarcoma risk genes using a two-stage genome wide DNA sequencing strategy in cancer cluster families and population case and control cohorts

International Sarcoma Kindred Study, 3 May 2019, In : BMC Medical Genetics. 20, 1, 10 p., 69.

Research output: Contribution to journalArticle

Open Access
Population Control
DNA Sequence Analysis
Sarcoma
Genome
Genes

INCREASED PREDICTED C4A EXPRESSION IS ASSOCIATED WITH COGNITIVE DEFICIT IN BOTH SCHIZOPHRENIA AND ALZHEIMER'S DISEASE

McCarthy, N., Laws, S. M., Porter, T., Burnham, S. C., Moses, E. K. & Jablensky, A., 2019, In : European Neuropsychopharmacology. 29, p. S871-S871 1 p.

Research output: Contribution to journalAbstract/Meeting Abstract

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways (vol 9, 4774, 2018)

Melanoma GWAS Consortium, 14 Jan 2019, In : Nature Communications. 10, 3 p., 299.

Research output: Contribution to journalComment/debate

Open Access

To test, or not to test: that is the question for the future of lipoprotein(a)

Ellis, K. L., Chakraborty, A., Moses, E. K. & Watts, G. F., 3 Apr 2019, In : Expert Review of Cardiovascular Therapy. 17, 4, p. 241-250 10 p.

Research output: Contribution to journalReview article

Lipoprotein(a)
Cardiovascular Diseases
Guidelines
Genetically Modified Animals
Expert Testimony

Whole-exome sequencing in multiplex preeclampsia families identifies novel candidate susceptibility genes

Melton, P. E., Johnson, M. P., Gokhale-Agashe, D., Rea, A. J., Ariff, A., Cadby, G., Peralta, J. M., Mcnab, T. J., Allcock, R. J., Abraham, L. J., Blangero, J., Brennecke, S. P. & Moses, E. K., 9 Jan 2019, In : Journal of Hypertension. 15 p.

Research output: Contribution to journalArticle

Exome
Pre-Eclampsia
Genes
Chromosomes, Human, Pair 1
Open Reading Frames
2018
1 Citation (Scopus)
34 Downloads (Pure)
Open Access
File
Personality Assessment
Endophenotypes
Cognition
Schizophrenia
Personality
3 Citations (Scopus)
Open Access
Congenital Heart Defects
MicroRNAs
Atrial Heart Septal Defects
Defects
Cardiovascular Diseases
1 Citation (Scopus)

Genetic approaches in preeclampsia

Yong, H. E. J., Murthi, P., Brennecke, S. P. & Moses, E. K., 1 Jan 2018, Genetic Approaches in Preeclampsia. Murthi, P. & Vaillancourt, C. (eds.). Humana Press, Vol. 1710. p. 53-72 20 p. (Methods in Molecular Biology; vol. 1710).

Research output: Chapter in Book/Conference paperChapter

Pre-Eclampsia
Causality
Genes
Research Personnel
Genome
51 Downloads (Pure)

Identification of Pre-eclampsia susceptibility genes

Gokhale-Agashe, D. S., 2018, (Unpublished)

Research output: ThesisDoctoral Thesis

File
Pre-Eclampsia
Genes
Collagen Type IV
Genome
Pregnancy
2 Citations (Scopus)

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Melanoma GWAS Consortium, 1 Dec 2018, In : Nature Communications. 9, 1, 4774.

Research output: Contribution to journalArticle

Open Access
Nevi and Melanomas
loci
Nevus
Melanoma
genes
1 Citation (Scopus)

Pleiotropy of cardiometabolic syndrome with obesity-related anthropometric traits determined using empirically derived kinships from the Busselton Health Study

Cadby, G., Melton, P. E., McCarthy, N. S., Almeida, M., Williams-Blangero, S., Curran, J. E., VandeBerg, J. L., Hui, J., Beilby, J., Musk, A. W., James, A. L., Hung, J., Blangero, J. & Moses, E. K., 2018, In : Human Genetics. 137, 1, p. 45–53 9 p.

Research output: Contribution to journalArticle

Obesity
Health
Single Nucleotide Polymorphism
Triglycerides
Body Mass Index
1 Citation (Scopus)
Genetic Heterogeneity
Schizophrenia
Genome
Psychotic Disorders
Base Pairing
2017
3 Citations (Scopus)

ADAM19: A novel target for metabolic syndrome in humans and mice

Weerasekera, L., Rudnicka, C., Sang, Q. X., Curran, J. E., Johnson, M. P., Moses, E. K., Göring, H. H. H., Blangero, J., Hricova, J., Schlaich, M. & Matthews, V. B., 7 Feb 2017, In : Mediators of Inflammation. 2017, 9 p., 7281986.

Research output: Contribution to journalArticle

Open Access
Disintegrins
Metalloproteases
Insulin Resistance
Obesity
Type 2 Diabetes Mellitus
3 Citations (Scopus)

Environment changes genetic effects on respiratory conditions and allergic phenotypes

Song, Y., Schwager, M. J., Backer, V., Guo, J., Porsbjerg, C., Khoo, S. K., Laing, I. A., Moses, E. K., LeSouëf, P. & Zhang, G., 24 Jul 2017, In : Scientific Reports. 7, 1, 6342.

Research output: Contribution to journalArticle

Open Access
Bronchitis
Phenotype
Single Nucleotide Polymorphism
Population
Genetic Association Studies
6 Citations (Scopus)
Exome
Schizophrenia
Genetic Association Studies
Gene Frequency
Population
Open Access
3 Citations (Scopus)

The antihypertensive MTHFR gene polymorphism rs17367504-G is a possible novel protective locus for preeclampsia

Thomsen, L. C. V., McCarthy, N. S., Melton, P. E., Cadby, G., Austgulen, R., Nygård, O. K., Johnson, M. P., Brennecke, S., Moses, E. K., Bjørge, L. & Iversen, A-C., Jan 2017, In : Journal of Hypertension. 35, 1, p. 132-139 8 p.

Research output: Contribution to journalArticle

Open Access
Methylenetetrahydrofolate Reductase (NADPH2)
Pre-Eclampsia
Antihypertensive Agents
Genes
Single Nucleotide Polymorphism
3 Citations (Scopus)

The Ark: a customizable web-based data management tool for health and medical research

Bickerstaffe, A., Ranaweera, T., Endersby, T., Ellis, C., Maddumarachchi, S., Gooden, G. E., White, P., Moses, E. K., Hewitt, A. W. & Hopper, J. L., 15 Feb 2017, In : Bioinformatics. 33, 4, p. 624-626 3 p.

Research output: Contribution to journalArticle

7 Citations (Scopus)

TRAK2, a novel regulator of ABCA1 expression, cholesterol efflux and HDL biogenesis

Lake, N. J., Taylor, R. L., Trahair, H., Harikrishnan, K. N., Curran, J. E., Almeida, M., Kulkarni, H., Mukhamedova, N., Hoang, A., Low, H., Murphy, A. J., Johnson, M. P., Dyer, T. D., Mahaney, M. C., Göring, H. H. H., Moses, E. K., Sviridov, D., Blangero, J., Jowett, J. B. M. & Bozaoglu, K., 21 Dec 2017, In : European Heart Journal. 38, 48, p. 3579–3587

Research output: Contribution to journalArticle

ATP Binding Cassette Transporter 1
Kinesin
Protein Binding
HDL Cholesterol
Cholesterol
2016
1 Citation (Scopus)
71 Downloads (Pure)

Finding potential cis-regulatory loci using allele-specific chromatin accessibility as weights in a kernel-based variance component test

Peralta, J. M., Almeida, M., Abraham, L. J., Moses, E. & Blangero, J., 2016, BMC Proceedings. Greenwood, C. M. T., MacCluer, J. W. & Almasy, L. (eds.). S7 ed. London: BioMed Central, Vol. 10. 50

Research output: Chapter in Book/Conference paperConference paper

Open Access
File
Deoxyribonuclease I
Polymorphism
Chromatin
Single Nucleotide Polymorphism
Nucleotides

Genetic Correlation of Lung Function with Anthropometric Measures in the Busselton Health Study

Cadby, G., Melton, P. E., McCarthy, N. S., Hui, J., Beilby, J., Musk, A. B., James, A. L., Hung, J., Blangero, J. & Moses, E. K., Nov 2016, In : Genetic Epidemiology. 40, 7, p. 625-626 2 p.

Research output: Contribution to journalAbstract/Meeting Abstract

3 Citations (Scopus)

GWAS and transcriptional analysis prioritize ITPR1 and CNTN4 for a serum uric acid 3p26 QTL in Mexican Americans

Chittoor, G., Kent, J. W., Almeida, M., Puppala, S., Farook, V. S., Cole, S. A., Haack, K., Göring, H. H. H., MacCluer, J. W., Curran, J. E., Carless, M. A., Johnson, M. P., Moses, E. K., Almasy, L., Mahaney, M. C., Lehman, D. M., Duggirala, R., Comuzzie, A. G., Blangero, J. & Voruganti, V. S., 2016, In : BMC Genomics. 17, 1, 276.

Research output: Contribution to journalArticle

Genome-Wide Association Study
Uric Acid
Serum
Kidney Calculi
Gout
9 Citations (Scopus)

Omics-squared: Human genomic, transcriptomic and phenotypic data for genetic analysis workshop 19

Blangero, J., Teslovich, T. M., Sim, X., Almeida, M. A., Jun, G., Dyer, T. D., Johnson, M. P., Peralta, J. M., Manning, A. K., Wood, A. R., Fuchsberger, C., Kent, J. W., Aguilar, D. A., Below, J. E., Farook, V. S., Arya, R., Fowler, S., Blackwell, T. W., Puppala, S., Kumar, S. & 13 othersGlahn, D. C., Moses, E. K., Curran, J. E., Thameem, F., Jenkinson, C. P., DeFronzo, R. A., Lehman, D. M., Hanis, C., Abecasis, G. R., Boehnke, M., Göring, H. H. H., Duggirala, R. & Almasy, L., 18 Oct 2016, Genetic Analysis Workshop 19: Sequence, Blood Pressure and Expression Data: Proceedings. 20 ed. BMC Proceedings, Vol. 10 (Supplement 7). p. 71-77

Research output: Chapter in Book/Conference paperConference paper

Open Access
Exome
Genes
Blood Pressure
Phenotype
Education

Preeclampsia does not share common risk alleles in 9p21 with coronary artery disease and type 2 diabetes

Kaartokallio, T., Lokki, A. I., Peterson, H., Kivinen, K., Hiltunen, L., Salmela, E., Lappalainen, T., Maanselkä, P., Heino, S., Knuutila, S., Sayed, A., Poston, L., Brennecke, S. P., Johnson, M. P., Morgan, L., Moses, E., Kere, J. & Laivuori, H., 25 Apr 2016, In : Annals of Medicine. 48, 5, p. 330-336 7 p.

Research output: Contribution to journalArticle

Pre-Eclampsia
Type 2 Diabetes Mellitus
Coronary Artery Disease
Alleles
Single Nucleotide Polymorphism
2015
16 Citations (Scopus)

Absence of germline mutations in BAP1 in sporadic cases of malignant mesothelioma

Sneddon, S., Leon, J., Dick, I., Cadby, G., Olsen, N., Brims, F., Allcock, R., Moses, E., Melton, P., De Klerk, N., Musk, A., Robinson, B. & Creaney, J., 25 May 2015, In : Gene. 563, 1, p. 103-105

Research output: Contribution to journalArticle

Open Access
Germ-Line Mutation
Mesothelioma
Exome
High-Throughput Nucleotide Sequencing
Neoplasms

A genetic connection between preeclampsia and chronic hypertension in Norwegian families.

Thomsen, L. C., Mccarthy, N., Melton, P., Tollaksen, K., Lyslo, I., Solberg, P., Roten, L. T., Nygard, O. K., Cadby, G., Austgulen, R., Moses, E., Iversen, A. C. & Bjorge, L., 2015, Abstracts of the XIXth World Congress for the Study of Hypertension in Pregnancy Preeclampsia/Hypertension - Future Risks and Novel Therapies. Netherlands: Elsevier, Vol. 5. p. 1

Research output: Chapter in Book/Conference paperConference paper

6 Citations (Scopus)

Effects of copy number variable regions on local gene expression in white blood cells of Mexican Americans

Blackburn, A., Almeida, M., Dean, A., Curran, J. E., Johnson, M. P., Moses, E., Abraham, L., Carless, M. A., Dyer, T. D., Kumar, S., Almasy, L., Mahaney, M. C., Comuzzie, A., Williams-Blangero, S., Blangero, J., Lehman, D. M. & Göring, H. H. H., 2015, In : European Journal of Human Genetics. 23, p. 1229-1235

Research output: Contribution to journalArticle

5 Citations (Scopus)

Genome-wide genetic investigation of serological measures of common infections

Rubicz, R., Yolken, R., Drigalenko, E., Carless, M. A., Dyer, T. D., Kent Jr, J., Curran, J. E., Johnson, M. P., Cole, S. A., Fowler, S. P., Arya, R., Puppala, S., Almasy, L., Moses, E., Kraig, E., Duggirala, R., Blangero, J., Leach, C. T. & Göring, H. H. H., 2015, In : European Journal of Human Genetics. 23, p. 1544-1548

Research output: Contribution to journalArticle

81 Citations (Scopus)

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma

Law, M. H., Bishop, D. T., Lee, J. E., Brossard, M., Martin, N. G., Moses, E., Song, F., Barrett, J. H., Kumar, R., Easton, D. F., Pharoah, P. D. P., Swerdlow, A. J., Kypreou, K. P., Taylor, J. C., Harland, M., Randerson-Moor, J., Akslen, L. A., Andresen, P. A., Avril, M. F., Azizi, E. & 55 othersScarrà, G. B., Brown, K. M., Dębniak, T., Duffy, D. L., Elder, D. E., Fang, S., Friedman, E., Galan, P., Ghiorzo, P., Gillanders, E. M., Goldstein, A. M., Gruis, N. A., Hansson, J., Helsing, P., Hočevar, M., Höiom, V., Ingvar, C., Kanetsky, P. A., Chen, W. V., Landi, M. T., Lang, J., Lathrop, G. M., Lubiński, J., Mackie, R. M., Mann, G. J., Molven, A., Montgomery, G. W., Novaković, S., Olsson, H., Puig, S., Puig-Butille, J. A., Qureshi, A. A., Radford-Smith, G. L., Van Der Stoep, N., Van Doorn, R., Whiteman, D. C., Craig, J. E., Schadendorf, D., Simms, L. A., Burdon, K. P., Nyholt, D. R., Pooley, K. A., Orr, N., Stratigos, A. J., Cust, A. E., Ward, S., Hayward, N. K., Han, J., Schulze, H. J., Dunning, A. M., Bishop, J. A. N., Demenais, F., Amos, C. I., Macgregor, S. & Iles, M. M., 2015, In : Nature Genetics. 47, 9, p. 987-995

Research output: Contribution to journalArticle

Meta-Analysis
Genome
Genome-Wide Association Study
Quantitative Trait Loci
Melanocytes

Genome-wide transcriptome directed pathway analysis of maternal preeclampsia susceptibility genes

Yong, H. E. J., Melton, P., Johnson, M. P., Freed, K. A., Kalionis, B., Murthi, P., Brennecke, S. P., Keogh, R. J. & Moses, E., 2015, XIXth World Congress for the Study of Hypertension in Pregnancy — Preeclampsia/Hypertension - Future Risks and Novel Therapies. Netherlands: Elsevier, Vol. 5. p. 1

Research output: Chapter in Book/Conference paperConference paper

19 Citations (Scopus)

Genome-wide transcriptome directed pathway analysis of maternal pre-eclampsia susceptibility genes

Yong, H. E. J., Melton, P., Johnson, M. P., Freed, K. A., Kalionis, B., Murthi, P., Brennecke, S. P., Keogh, R. J. & Moses, E., 26 May 2015, In : PLoS One. 10, 5, p. 1-15

Research output: Contribution to journalArticle

Open Access
pre-eclampsia
Pre-Eclampsia
Transcriptome
transcriptome
Genes
6 Citations (Scopus)

Refined phenotyping identifies links between preeclampsia and related diseases in a Norwegian preeclampsia family cohort

Thomsen, L. C. V., Melton, P., Tollaksen, K., Lyslo, I., Roten, L. T., Odland, M. L., Strand, K. M., Nygard, O., Sun, C., Iversen, A. C., Austgulen, R., Moses, E. & Bjørge, L., 2015, In : Journal of Hypertension. 33, 11, p. 2294-2302

Research output: Contribution to journalArticle

Open Access
Pre-Eclampsia
Gestational Age
Phenotype
Cardiovascular Diseases
Lung Diseases
125 Citations (Scopus)

The transcriptional landscape of age in human peripheral blood

Peters, M. J., Joehanes, R., Pilling, L. C., Schurmann, C., Conneely, K. N., Powell, J., Reinmaa, E., Sutphin, G. L., Zhernakova, A., Schramm, K., Wilson, Y. A., Kobes, S., Tukiainen, T., Ramos, Y. F., Göring, H. H. H., Fornage, M., Liu, Y., Gharib, S. A., Stranger, B. E., De Jager, P. L. & 52 othersAviv, A., Levy, D., Murabito, J. M., Munson, P. J., Huan, T., Hofman, A., Uitterlinden, A. G., Rivadeneira, F., Van Rooij, J., Stolk, L., Broer, L., Verbiest, M. M. P. J., Jhamai, M., Arp, P., Metspalu, A., Tserel, L., Milani, L., Samani, N. J., Peterson, P., Kasela, S., Codd, V., Peters, A., Ward-Caviness, C. K., Herder, C., Waldenberger, M., Roden, M., Singmann, P., Zeilinger, S., Illig, T., Homuth, G., Grabe, H. J., Völzke, H., Steil, L., Kocher, T., Murray, A., Melzer, D., Yaghootkar, H., Bandinelli, S., Moses, E., Kent, J. W., Curran, J. E., Johnson, M. P., Williams-Blangero, S., Westra, H. J., Mcrae, A. F., Smith, J. A., Kardia, S. L. R., Hovatta, I., Perola, M., Ripatti, S., Salomaa, V. & Henders, A. K., 2015, In : Nature Communications. 6, p. 8570

Research output: Contribution to journalArticle

Open Access
gene expression
Gene expression
genes
blood
methylation
2014

FURTHER EVIDENCE FOR THE INVOLVEMENT OF TWO FUNCTIONAL POLYMORPHISMS IN FOLATE METABOLISING GENES, SHMT1(1420)T AND MTRR(66)A, WITH AN INCREASED RISK OF EARLY SPONTANEOUS PRETERM BIRTH FROM THE PGP CONSORTIUM GWAS: PS512

Cunneen, R. J., Ang, Q. W., White, M. K., Menon, R., Merialdi, M., Williams, S. M., Katz, M., Lye, S. J., Olson, D., Moses, E. K., Pennell, C. E. & McCarthy, N., 2014, p. 44.

Research output: Contribution to conferencePoster

Further Evidence for the Involvement of Two Functional Polymorphisms in Folate Metabolising Genes, SHMT1 (1420) T and MTRR (66) A, with an Increased Risk of Early Spontaneous Preterm Birth from the PGP Consortium GWAS: T-076

McCarthy, N., Cunneen, R. J., Ang, W., White, M. K., Merialdi, M., Katz, M., Williams, S., Olson, D., Lye, S. J., Menon, R., Moses, E. & Pennell, C. E., 2014, p. 154A.

Research output: Contribution to conferencePoster

3 Citations (Scopus)

Genome-wide genetic and transcriptomic investigation of variation in antibody response to dietary antigens

Rubicz, R. C., Yolken, R. H., Alaedini, A., Drigalenko, E. I., Charlesworth, J. C., Carless, M. A., Severance, E. G., Krivogorsky, B., Dyer, T. D., Kent, J. W., Curran, J. E., Johnson, M. P., Cole, S. A., Almasy, L., Moses, E., Blangero, J. & Göring, H. H. H., 2014, In : Genetic Epidemiology. 38, 5, p. 439-446

Research output: Contribution to journalArticle

Antibody Formation
Genome
Antigens
Immunoglobulin G
Antibodies
12 Citations (Scopus)

Increased decidual mRNA expression levels of candidate maternal pre-eclampsia susceptibility genes are associated with clinical severity

Yong, H. E. J., Murthi, P., Borg, A., Kalionis, B., Moses, E., Brennecke, S. P. & Keogh, R. J., 2014, In : Placenta. 35, 2, p. 117-124

Research output: Contribution to journalArticle

27 Citations (Scopus)

MACROD2 gene associated with autistic-like traits in a general population sample

Jones, R., Cadby, G., Blangero, J., Abraham, L., Whitehouse, A. & Moses, E., Dec 2014, In : Psychiatric Genetics. 24, 6, p. 241-248

Research output: Contribution to journalArticle

Open Access
Autistic Disorder
Single Nucleotide Polymorphism
Population
Genes
Cohort Studies
29 Citations (Scopus)

Meta-analysis of human methylation data for evidence of sex-specific autosomal patterns

Mccarthy, N., Melton, P., Cadby, G., Yazar, S., Franchina, M., Moses, E., Mackey, D. & Hewitt, A., 18 Nov 2014, In : BMC Genomics. 15, p. 1-11 12 p., 981.

Research output: Contribution to journalArticle

Open Access
5 Citations (Scopus)

Molecular prioritization strategies to identify functional genetic variants in the cardiovascular disease-associated expression QTL Vanin-1

Kaskow, B. J., Diepeveen, L. A., Michael Proffitt, J. M., Rea, S., Ulgiati, D., Blangero, J., Moses, E. & Abraham, L., 2014, In : European Journal of Human Genetics. In Press, p. 8pp

Research output: Contribution to journalArticle

5 Citations (Scopus)

Plasma levels of soluble interleukin 1 receptor accessory protein are reduced in obesity

Bozaoglu, K., Attard, C., Kulkarni, H., Cummings, N., Diego, V. P., Carless, M. A., Shields, K. A., Johnson, M. P., Kowlessur, S., Dyer, T. D., Comuzzie, A. G., Almasy, L., Zimmet, P., Moses, E., Göring, H. H. H., Curran, J. E., Blangero, J. & Jowett, J. B. M., 2014, In : Journal of Clinical Endocrinology and Metabolism. 99, p. 3435-3443

Research output: Contribution to journalArticle

7 Citations (Scopus)

Preeclampsia and cardiovascular disease share genetic risk factors on chromosome 2q22

Løset, M., Johnson, M. P., Melton, P., Ang, W., Huang, R-C., Mori, T., Beilin, L., Pennell, C., Roten, L. T., Iversen, A. C., Austgulen, R., East, C. E., Blangero, J. C., Brennecke, S. P. & Moses, E., 2014, In : Pregnancy Hypertension. 4, 2, p. 178-185

Research output: Contribution to journalArticle

Pre-Eclampsia
Single Nucleotide Polymorphism
Cardiovascular Diseases
Chromosomes
Mothers
7 Citations (Scopus)
67 Citations (Scopus)

The effect on melanoma risk of genes previously associated with telomere length

Iles, M. M., Bishop, D. T., Taylor, J. C., Hayward, N. K., Brossard, M., Cust, A. E., Dunning, A. M., Lee, J. E., Moses, E., Akslen, L. A., Andresen, P. A., Avril, M. F., Azizi, E., Scarrà, G. B., Brown, K. M., Debniak, T., Elder, D. E., Friedman, E., Ghiorzo, P., Gillanders, E. M. & 36 othersGoldstein, A. M., Gruis, N. A., Hansson, J., Harland, M., Helsing, P., Hočevar, M., Höiom, V., Ingvar, C., Kanetsky, P. A., Landi, M. T., Lang, J., Lathrop, G. M., Lubiński, J., Mackie, R. M., Martin, N. G., Molven, A., Montgomery, G. W., Novaković, S., Olsson, H., Puig, S., Puig-Butille, J. A., Radford-Smith, G. L., Randerson-Moor, J., Van Der Stoep, N., Van Doorn, R., Whiteman, D. C., Macgregor, S., Pooley, K. A., Ward, S., Mann, G. J., Amos, C. I., Pharoah, P. D., Demenais, F., Law, M. H., Newton Bishop, J. A. & Barrett, J. H., Oct 2014, In : Journal of the National Cancer Institute. 106, 10, p. 1-5

Research output: Contribution to journalArticle

Open Access
Telomere
Melanoma
Single Nucleotide Polymorphism
Genes
Israel
269 Citations (Scopus)

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

Thompson, P. M., Stein, J. L., Medland, S. E., Hibar, D. P., Vasquez, A. A., Renteria, M. E., Toro, R., Jahanshad, N., Schumann, G., Franke, B., Wright, M. J., Martin, N. G., Agartz, I., Alda, M., Alhusaini, S., Almasy, L., Almeida, J., Alpert, K., Andreasen, N. C., Andreassen, O. A. & 269 othersApostolova, L. G., Appel, K., Armstrong, N. J., Aribisala, B., Bastin, M. E., Bauer, M., Bearden, C. E., Bergmann, O., Binder, E. B., Blangero, J., Bockholt, H. J., Bøen, E., Bois, C., Boomsma, D. I., Booth, T., Bowman, I. J., Bralten, J., Brouwer, R. M., Brunner, H. G., Brohawn, D. G., Buckner, R. L., Buitelaar, J., Bulayeva, K., Bustillo, J. R., Calhoun, V. D., Cannon, D. M., Cantor, R. M., Carless, M. A., Caseras, X., Cavalleri, G. L., Chakravarty, M. M., Chang, K. D., Ching, C. R. K., Christoforou, A., Cichon, S., Clark, V. P., Conrod, P., Coppola, G., Crespo-Facorro, B., Curran, J. E., Czisch, M., Deary, I. J., De Geus, E. J. C., Den Braber, A., Delvecchio, G., Depondt, C., De Haan, L., De Zubicaray, G. I., Dima, D., Dimitrova, R., Djurovic, S., Dong, H., Donohoe, G., Duggirala, R., Dyer, T. D., Ehrlich, S., Ekman, C. J., Elvsåshagen, T., Emsell, L., Erk, S., Espeseth, T., Fagerness, J., Fears, S., Fedko, I., Fernández, G., Fisher, S. E., Foroud, T., Fox, P. T., Francks, C., Frangou, S., Frey, E. M., Frodl, T., Frouin, V., Garavan, H., Giddaluru, S., Glahn, D. C., Godlewska, B., Goldstein, R. Z., Gollub, R. L., Grabe, H. J., Grimm, O., Gruber, O., Guadalupe, T., Gur, R. E., Gur, R. C., Göring, H. H. H., Hagenaars, S., Hajek, T., Hall, G. B., Hall, J., Hardy, J., Hartman, C. A., Hass, J., Hatton, S. N., Haukvik, U. K., Hegenscheid, K., Heinz, A., Hickie, I. B., Ho, B-C., Hoehn, D., Hoekstra, P. J., Hollinshead, M., Holmes, A. J., Homuth, G., Hoogman, M., Hong, L. E., Hosten, N., Hottenga, J-J., Hulshoff Pol, H. E., Hwang, K. S., Jack Jr., C. R., Jenkinson, M., Johnston, C., Jönsson, E. G., Kahn, R. S., Kasperaviciute, D., Kelly, S., Kim, S., Kochunov, P., Koenders, L., Krämer, B., Kwok, J. B. J., Lagopoulos, J., Laje, G., Landen, M., Landman, B. A., Lauriello, J., Lawrie, S. M., Lee, P. H., Le Hellard, S., Lemaître, H., Leonardo, C. D., Li, C., Liberg, B., Liewald, D. C., Liu, X., Lopez, L. M., Loth, E., Lourdusamy, A., Luciano, M., Macciardi, F., Machielsen, M. W. J., Macqueen, G. M., Malt, U. F., Mandl, R., Manoach, D. S., Martinot, J-L., Matarin, M., Mather, K. A., Mattheisen, M., Mattingsdal, M., Meyer-Lindenberg, A., Mcdonald, C., Mcintosh, A. M., Mcmahon, F. J., Mcmahon, K. L., Meisenzahl, E., Melle, I., Milaneschi, Y., Mohnke, S., Montgomery, G. W., Morris, D. W., Moses, E., Mueller, B. A., Muñoz Maniega, S., Mühleisen, T. W., Müller-Myhsok, B., Mwangi, B., Nauck, M., Nho, K., Nichols, T. E., Nilsson, L-G., Nugent, A. C., Nyberg, L., Olvera, R. L., Oosterlaan, J., Ophoff, R. A., Pandolfo, M., Papalampropoulou-Tsiridou, M., Papmeyer, M., Paus, T., Pausova, Z., Pearlson, G. D., Penninx, B. W., Peterson, C. P., Pfennig, A., Phillips, M., Pike, G. B., Poline, J-B., Potkin, S. G., Pütz, B., Ramasamy, A., Rasmussen, J., Rietschel, M., Rijpkema, M., Risacher, S. L., Roffman, J. L., Roiz-Santiañez, R., Romanczuk-Seiferth, N., Rose, E. J., Royle, N. A., Rujescu, D., Ryten, M., Sachdev, P. S., Salami, A., Satterthwaite, T. D., Savitz, J., Saykin, A. J., Scanlon, C., Schmaal, L., Schnack, H. G., Schork, A. J., Schulz, S. C., Schür, R., Seidman, L., Shen, L., Shoemaker, J. M., Simmons, A., Sisodiya, S. M., Smith, C., Smoller, J. W., Soares, J. C., Sponheim, S. R., Sprooten, E., Starr, J. M., Steen, V. M., Strakowski, S., Strike, L., Sussmann, J., Sämann, P. G., Teumer, A., Toga, A. W., Tordesillas-Gutierrez, D., Trabzuni, D., Trost, S., Turner, J., Van Den Heuvel, M., Van Der Wee, N. J., Van Eijk, K., Van Erp, T. G. M., Van Haren, N. E. M., Van 'T Ent, D., Van Tol, M-J., Valdés Hernández, M. C., Veltman, D. J., Versace, A., Völzke, H., Walker, R., Walter, H., Wang, L., Wardlaw, J. M., Weale, M. E., Weiner, M. W., Wen, W., Westlye, L. T., Whalley, H. C., Whelan, C. D., White, T., Winkler, A. M., Wittfeld, K., Woldehawariat, G., Wolf, C., Zilles, D., Zwiers, M. P., Thalamuthu, A., Schofield, P. R., Freimer, N. B., Lawrence, N. S. & Drevets, W., 2014, In : Brain Imaging and Behavior. 8, p. 153-82

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