Works matching DE "GENETICS -- Risk factors"

Results: 43

Epidemiology of Parkinson's disease.

Published in:

Journal of Neural Transmission, 2017, v. 124, n. 8, p. 901, doi. 10.1007/s00702-017-1686-y

By:

Tysnes, Ole-Bjørn;
Storstein, Anette

Publication type:

Article

Straight talk with...Daniel Levy.

Published in:: Nature Medicine, 2013, v. 19, n. 10, p. 1197, doi. 10.1038/nm1013-1197
Publication type:: Article

Additive and interaction effects at three amino acid positions in HLA-DQ and HLA-DR molecules drive type 1 diabetes risk.

Published in:

Nature Genetics, 2015, v. 47, n. 8, p. 898, doi. 10.1038/ng.3353

By:

Hu, Xinli;
Deutsch, Aaron J;
Lenz, Tobias L;
Onengut-Gumuscu, Suna;
Chen, Wei-Min;
Rich, Stephen S;
Han, Buhm;
Howson, Joanna M M;
Todd, John A;
de Bakker, Paul I W;
Raychaudhuri, Soumya

Publication type:

Article

Corrigendum: Statistical colocalization of genetic risk variants for related autoimmune diseases in the context of common controls.

Published in:

Nature Genetics, 2015, v. 47, n. 8, p. 962, doi. 10.1038/ng0815-962c

By:

Fortune, Mary D;
Guo, Hui;
Burren, Oliver;
Schofield, Ellen;
Walker, Neil M;
Ban, Maria;
Sawcer, Stephen J;
Bowes, John;
Worthington, Jane;
Barton, Anne;
Eyre, Steve;
Todd, John A;
Wallace, Chris

Publication type:

Article

Genetic susceptibility to lung cancer—light at the end of the tunnel?

Published in:

Carcinogenesis, 2013, v. 34, n. 3, p. 487, doi. 10.1093/carcin/bgt016

By:

Marshall, Ariela L.;
Christiani, David C.

Publication type:

Article

Non-Replication of Genome-Wide Based Associations between Common Variants in INSIG2 and PFKP and Obesity in Studies of 18,014 Danes.

Published in:

PLoS ONE, 2008, v. 3, n. 8, p. 1, doi. 10.1371/journal.pone.0002872

By:

Andreasen, Camilla H.;
Mogensen, Mette S.;
Borch-Johnsen, Knut;
Sandbæk, Annelli;
Lauritzen, Torsten;
Sørensen, Thorkild I. A.;
Hansen, Lars;
Almind, Katrine;
Jørgensen, Torben;
Pedersen, Oluf;
Hansen, Torben

Publication type:

Article

Long-Term Follow-Up of Intrauterine Growth Restriction: Cardiovascular Disorders.

Published in:

Fetal Diagnosis & Therapy, 2014, v. 36, n. 2, p. 143, doi. 10.1159/000353633

By:

Demicheva, Elena;
Crispi, Fatima

Publication type:

Article

Simple, standardized incorporation of genetic risk into non-genetic risk prediction tools for complex traits: coronary heart disease as an example.

Published in:

Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00254

By:

Goldstein, Benjamin A.;
Knowles, Joshua W.;
Salfati, Elias;
Ioannidis, John P. A.;
Assimes, Themistocles L.

Publication type:

Article

Poster Session PA3.

Published in:: Alcohol & Alcoholism. Supplement, 2007, v. 42, p. i51, doi. 10.1093/alcalc/agm127
Publication type:: Article

Homozygous truncation of SIX6 causes complex microphthalmia in humans.

Published in:

Clinical Genetics, 2013, v. 84, n. 2, p. 198, doi. 10.1111/cge.12046

By:

Aldahmesh, M A;
Khan, A O;
Hijazi, H;
Alkuraya, F S

Publication type:

Article

Biochemical and genetic aspects of pathogenesis of schizophrenia.

Published in:

Journal of Evolutionary Biochemistry & Physiology, 2011, v. 47, n. 5, p. 407, doi. 10.1134/S0022093011050021

By:

Kambarova, D.;
Golubev, A.

Publication type:

Article

Do Late Bubbles Correspond to Early Hepatopulmonary Syndrome?

Published in:

Annals of Hepatology: Official Journal of the Mexican Association of Hepatology, 2017, v. 16, n. 4, p. 476, doi. 10.5604/01.3001.0010.0268

By:

DuBrock, Hilary M.;
Krowka, Michael J.

Publication type:

Article

Missing heritability and strategies for finding the underlying causes of complex disease.

Published in:

2010

By:

Eichler, Evan E.;
Flint, Jonathan;
Gibson, Greg;
Kong, Augustine;
Leal, Suzanne M.;
Moore, Jason H.;
Nadeau, Joseph H.

Publication type:

research

Use of allele scores as instrumental variables for Mendelian randomization.

Published in:

International Journal of Epidemiology, 2013, v. 42, n. 4, p. 1134, doi. 10.1093/ije/dyt093

By:

Burgess, Stephen;
Thompson, Simon G

Publication type:

Article

Strengthening the reporting of genetic risk prediction studies (GRIPS): explanation and elaboration.

Published in:

European Journal of Human Genetics, 2011, v. 19, n. 5, p. 1, doi. 10.1038/ejhg.2011.27

By:

Janssens, A. Cecile J. W.;
Ioannidis, John P. A.;
Bedrdosian, Sara;
Boffetta, Paolo;
Dolan, Siobhan M.;
Dowling, Nicole;
Fortier, Isabel;
Freedman, Andrew N.;
Grimshaw, Jeremy M.;
Gulcher, Jeffrey;
Gwinn, Marta;
Hlatky, Mark A.;
Janes, Holly;
Kraft, Peter;
Melillo, Stephanie;
O'Donnell, Christopher J.;
Pencina, Michael J.;
Ransohoff, David;
Schully, Sheri D.;
Seminara, Daniela

Publication type:

Article

Loss of asymmetry in D<sub>2</sub> receptors of putamen in unaffected family members at increased genetic risk for schizophrenia.

Published in:

Acta Psychiatrica Scandinavica, 2008, v. 118, n. 3, p. 200, doi. 10.1111/j.1600-0447.2008.01223.x

By:

Lee, K. J.;
Lee, J. S.;
Kim, S. J.;
Correll, C. U.;
Wee, H.;
Yoo, S. Y.;
Jeong, J. M.;
Lee, D. S.;
Lee, S. I.;
Kwon, J. S.

Publication type:

Article

Major psychoses with mixed psychotic and mood symptoms: are mixed psychoses associated with different neurobiological markers?

Published in:

Acta Psychiatrica Scandinavica, 2008, v. 118, n. 3, p. 172, doi. 10.1111/j.1600-0447.2008.01230.x

By:

Bora, E.;
Yucel, M.;
Fornito, A.;
Berk, M.;
Pantelis, C.

Publication type:

Article

A common haplotype of the C-C chemokine receptor 2 gene and HLA-DRB1*0301 are independent genetic risk factors for Löfgren’s syndrome.

Published in:

Journal of Internal Medicine, 2008, v. 264, n. 5, p. 433, doi. 10.1111/j.1365-2796.2008.01984.x

By:

Spagnolo, P.;
Sato, H.;
Grunewald, J.;
Brynedal, B.;
Hillert, J.;
Mañá, J.;
Wells, A. U.;
Eklund, A.;
Welsh, K. I.;
du Bois, R. M.

Publication type:

Article

Strengthening the reporting of genetic risk prediction studies: the GRIPS statement.

Published in:

European Journal of Clinical Investigation, 2011, v. 41, n. 9, p. 1004, doi. 10.1111/j.1365-2362.2011.02494.x

By:

Janssens, A. Cecile J. W.;
Ioannidis, John P. A.;
van Duijn, Cornelia M.;
Little, Julian;
Khoury, Muin J.

Publication type:

Article

Prediction of leprosy in the Chinese population based on a weighted genetic risk score.

Published in:

PLoS Neglected Tropical Diseases, 2018, v. 12, n. 9, p. 1, doi. 10.1371/journal.pntd.0006789

By:

Fu, Xi'an;
Wang, Na;
Yue, Zhenhua;
Wang, Honglei;
Niu, Guiye;
Li, Jinghui;
Li, Zhen;
You, Jiabao;
Liu, Hong;
Zhang, Furen;
Chen, Mingfei;
Li, Furong;
Wang, Zhenzhen;
Wang, Chuan;
Yu, Gongqi;
Liu, Tingting;
Zhang, Huimin;
Li, Lulu;
Liu, Dan;
Zhang, Mingkai

Publication type:

Article

Multi-allelic haplotype model based on genetic partition for genomic prediction and variance component estimation using SNP markers.

Published in:

BMC Genetics, 2015, v. 16, p. 1, doi. 10.1186/s12863-015-0301-1

By:

Yang Da

Publication type:

Article

Machine learning algorithm-based risk prediction model of coronary artery disease.

Published in:

Molecular Biology Reports, 2018, v. 45, n. 5, p. 901, doi. 10.1007/s11033-018-4236-2

By:

Naushad, Shaik Mohammad;
Hussain, Tajamul;
Indumathi, Bobbala;
Samreen, Khatoon;
Alrokayan, Salman A.;
Kutala, Vijay Kumar

Publication type:

Article

The c.−190 C>A transversion in promoter region of protamine1 gene as a genetic risk factor for idiopathic oligozoospermia.

Published in:

Molecular Biology Reports, 2016, v. 43, n. 8, p. 795, doi. 10.1007/s11033-016-4017-8

By:

Jamali, Shirin;
Karimian, Mohammad;
Nikzad, Hossein;
Aftabi, Younes

Publication type:

Article

Genetic variants of eNOS gene may modify the susceptibility to idiopathic male infertility.

Published in:

Biomarkers, 2013, v. 18, n. 5, p. 412, doi. 10.3109/1354750X.2013.805245

By:

Ying, Hou-Qun;
Pu, Xiao-Ying;
Liu, Shuo-Ran;
A, Zhou-Cun

Publication type:

Article

Genetic risk factors for inhibitors in haemophilia A.

Published in:

European Journal of Haematology, 2015, v. 94, p. 7, doi. 10.1111/ejh.12495

By:

Bardi, Edit;
Astermark, Jan

Publication type:

Article

Thrombotic Thrombocytopenic Purpura in Black People: Impact of Ethnicity on Survival and Genetic Risk Factors.

Published in:

PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0156679

By:

Martino, Suella;
Jamme, Mathieu;
Deligny, Christophe;
Busson, Marc;
Loiseau, Pascale;
Azoulay, Elie;
Galicier, Lionel;
Pène, Frédéric;
Provôt, François;
Dossier, Antoine;
Saheb, Samir;
Veyradier, Agnès;
Coppo, Paul;
null, null

Publication type:

Article

Identification of genetic variants associated with dengue or West Nile virus disease: a systematic review and meta-analysis.

Published in:

2018

By:

Cahill, Megan E.;
Conley, Samantha;
DeWan, Andrew T.;
Montgomery, Ruth R.

Publication type:

journal article

Holistic management of osteoarthritis.

Published in:

Practice Nursing, 2008, v. 19, n. 6, p. 298, doi. 10.12968/pnur.2008.19.6.30276

By:

Oliver, Susan M.

Publication type:

Article

Hereditary breast cancer: ever more pieces to the polygenic puzzle.

Published in:

Hereditary Cancer in Clinical Practice, 2013, v. 11, n. 1, p. 1, doi. 10.1186/1897-4287-11-12

By:

Bogdanova, Natalia;
Helbig, Sonja;
Dörk, Thilo

Publication type:

Article

Let the Individuals Directly Concerned Decide: A Solution to Tragic Choices in Genetic Risk Information.

Published in:

Public Health Genomics, 2016, v. 19, n. 5, p. 307, doi. 10.1159/000448913

By:

Oliveri, Serena;
Pravettoni, Gabriella;
Fioretti, Chiara;
Hansson, Mats G.

Publication type:

Article

Applying a Theory-Based Framework to Understand Public Knowledge of Genetic Risk Factors: A Case for the Distinction between How-To Knowledge and Principles Knowledge.

Published in:

Public Health Genomics, 2011, v. 14, n. 4/5, p. 259, doi. 10.1159/000294149

By:

Smerecnik, C.M.R.;
Mesters, I.;
de Vries, N.K.;
de Vries, H.

Publication type:

Article

Is it Useful to Classify Progressive Supranuclear Palsy and Corticobasal Degeneration as Different Disorders? No.

Published in:

Movement Disorders Clinical Practice, 2018, v. 5, n. 2, p. 141, doi. 10.1002/mdc3.12582

By:

Höglinger, Günter U.

Publication type:

Article

Is it Useful to Classify PSP and CBD as Different Disorders? Yes.

Published in:

Movement Disorders Clinical Practice, 2018, v. 5, n. 2, p. 145, doi. 10.1002/mdc3.12581

By:

Ling, Helen;
Macerollo, Antonella

Publication type:

Article

Genetic Risk Factors for Longitudinal Changes in Structural MRI in Former Organolead Workers.

Published in:

Journal of Aging Research, 2011, p. 1, doi. 10.4061/2011/362189

By:

James, Bryan D.;
Caffo, Brian;
Stewart, Walter F.;
Yousem, David;
Davatzikos, Christos;
Schwartz, Brian S.

Publication type:

Article

EVALUATION OF GENETIC RISK FACTORS FOR CHILDHOOD ASTHMA USING GENERALIZED MULTIFACTOR DIMENSIONALITY REDUCTION SOFTWARE.

Published in:

Romanian Journal of Rheumatology / Revista Romana de Reumatologie, 2014, v. 23, n. 2, p. 148

By:

Cirstea, Olga;
Vasilos, Liubov;
Cojocaru, Ala;
Savoschin, Dorina

Publication type:

Article

Discovery of genetic risk factors for disease.

Published in:

Journal of the Royal Society of New Zealand, 2018, v. 48, n. 2/3, p. 191, doi. 10.1080/03036758.2017.1392324

By:

Montgomery, Grant W.

Publication type:

Article

Genetic factor common to schizophrenia and HIV infection is associated with risky sexual behavior: antagonistic vs. synergistic pleiotropic SNPs enriched for distinctly different biological functions.

Published in:

Human Genetics, 2017, v. 136, n. 1, p. 75, doi. 10.1007/s00439-016-1737-8

By:

Wang, Qian;
Polimanti, Renato;
Kranzler, Henry;
Farrer, Lindsay;
Zhao, Hongyu;
Gelernter, Joel

Publication type:

Article

Genetic risk score analysis indicates migraine with and without comorbid depression are genetically different disorders.

Published in:

Human Genetics, 2014, v. 133, n. 2, p. 173, doi. 10.1007/s00439-013-1370-8

By:

Ligthart, Lannie;
Hottenga, Jouke-Jan;
Lewis, Cathryn;
Farmer, Anne;
Craig, Ian;
Breen, Gerome;
Willemsen, Gonneke;
Vink, Jacqueline;
Middeldorp, Christel;
Byrne, Enda;
Heath, Andrew;
Madden, Pamela;
Pergadia, Michele;
Montgomery, Grant;
Martin, Nicholas;
Penninx, Brenda;
McGuffin, Peter;
Boomsma, Dorret;
Nyholt, Dale

Publication type:

Article

Missingness in the T1DGC MHC fine-mapping SNP data: association with HLA genotype and potential influence on genetic association studies.

Published in:

Diabetes, Obesity & Metabolism, 2009, v. 11, p. 101, doi. 10.1111/j.1463-1326.2008.01010.x

By:

James, I.;
McKinnon, E.;
Gaudieri, S.;
Morahan, G.

Publication type:

Article

Results of the MHC Fine Mapping Workshop.

Published in:

Diabetes, Obesity & Metabolism, 2009, v. 11, p. 108, doi. 10.1111/j.1463-1326.2008.01011.x

By:

Rich, S. S.;
Akolkar, B.;
Concannon, P.;
Erlich, H.;
Hilner, J.;
Julier, C.;
Morahan, G.;
Nerup, J.;
Nierras, C.;
Pociot, F.;
Todd, J. A.

Publication type:

Article

Setting the stage.

Published in:

Diabetes, Obesity & Metabolism, 2009, v. 11, p. 1, doi. 10.1111/j.1463-1326.2008.00996.x

By:

Rich, S. S.;
Nierras, C.;
Akolkar, B.

Publication type:

Article

Cancer risk in the relatives of patients with nasopharyngeal carcinoma-a register-based cohort study in Sweden.

Published in:

British Journal of Cancer, 2015, v. 112, n. 11, p. 1827, doi. 10.1038/bjc.2015.140

By:

Liu, Z;
Fang, F;
Chang, E T;
Ye, W

Publication type:

Article

Cdon Mutation and Fetal Ethanol Exposure Synergize to Produce Midline Signaling Defects and Holoprosencephaly Spectrum Disorders in Mice.

Published in:

PLoS Genetics, 2012, v. 8, n. 10, p. 1, doi. 10.1371/journal.pgen.1002999

By:

Mingi Hong;
Krauss, Robert S.

Publication type:

Article