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Molecular portraits of human breast tumours

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The sequence of the human genome

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Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease

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The Future of Genetic Studies of Complex Human Diseases

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A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease

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A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

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Amino Acid Difference Formula to Help Explain Protein Evolution

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Epidemiology in Medicine

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Listening to silence and understanding nonsense: exonic mutations that affect splicing

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Genetic Susceptibility to Neonatal Disease

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Papel de la medicina genómica en las enfermedades del oído medio e interno

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Farmacogenética do tratamento com hormônio de crescimento (GH) em crianças com deficiência de GH

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Interaction of Genetic Susceptibility and Traffic- Related Air Pollution in Cardiovascular Disease

Levinsson, A. (2015) · Gothenburg University Publications Electronic Archive (Gothenburg University)

Variantes genéticas de risco para a dependência de crack/cocaína: estudo de associação do tipo gene candidato e epistasia

Negrão, A. B. (2012) · Digital Library of Theses and Dissertations (Universidade de São Paulo) · doi:10.11606/t.5.2012.tde-25052012-143844

Epidemiologic Considerations in Complex Disease Genetics: Figure 1.Preprint

Gallacher, J. (2011) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top067512

SNP Discovery and Genotyping

Wang, J., Aud, D., Germer, S., & Higuchi, R. (2007) · Humana Press eBooks · doi:10.1007/978-1-59259-930-1_5

Similaridades entre o Transcriptoma Humano e Murino Focando Genes Situados em Regiões de Susceptibilidade ao Diabetes mellitus do Tipo 1

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Biomedical Informatics in chronic infectious and inflammatory disease research: periodontitis as a case study

Loos, B. G., Laine, M. L., van der Palen, C. J. N. M., Lessmann, F., Winkelhoff, A. J. V., van der Velden, U., Crusius, J. B. A., Morré, S. A., Peña, A. S., Brooks, A., et al. (2006) · UvA-DARE (University of Amsterdam)

Investigating the epidemiological and genetic overlap between obesity and alcohol consumption and addiction

Schierup, M. H., Grarup, N., & Johansen, M. (2015)

Genetic analysis in the horse Summer eczema and Dun coat color

Andersson, L. S. (2007)

Variation in sleep behaviour and its underlying causes: a study in a free-living blue tit population

Loës, C. (2012)

GENETICS OF CARDIOVASCULAR DISEASE

Kristiansson, K. (2008)

EDITORIALS Betting Odds and Genetic Associations

Thomas, D. C., & Clayton, D. G. (2013)

«In-vitro» functional studies of the «LTA+80A» leprosy risk factor

Clouatre, E. (2009) · doi:10.82308/40816

Phenotypic Diversity and Genetic Epidemiology of Placental Abruption

Toivonen, S. (2009)

Genetic and Expressional Studies of Alzheimer's Disease

Iivonen, S. (2005)

Statistical methods for family-based association studies for complex human diseases : single-locus and haplotype methods.

Chung, R. (2006) · NCSU Libraries Repository (North Carolina State University Libraries)

Computational prediction of gene targets for fetal alcohol spectrum disorders

Lombard, Z. (2010) · University of the Witwatersrand, Johannesburg Institutional Repository on DSpace (University of the Witwatersrand, Johannesburg)

Genetic association on radiation induced mucosal and skin toxicity in patients with nasopharyngeal carcinoma

Cheuk, I., & Wu, V. (2014) · Journal of Nasopharyngeal Carcinoma · doi:10.15383/jnpc.7

Investigating genetic determinants of phenotypic variation in natural isolates of Saccharomyces cerevisiae

Lee, H. (2012) · eScholarship (California Digital Library)

Development of Haplotype Reconstruction System Using Public Resources

Kim, K. (2010) · Journal of the Korea Academia-Industrial cooperation Society · doi:10.5762/kais.2010.11.2.720

Tumor necrosis factor-a −308 G/A polymorphism in a sample of Egyptian patients with Alzheimer′s disease

Rajab, A., Aty, A. A., Khalil, A., Missiry, A. E., Mohamed, N., & Hamrawy, L. E. (2015) · Egyptian Journal of Psychiatry · doi:10.4103/1110-1105.158116

Genetics of obesity in Hong Kong Chinese : a candidate gene approach focusing on the melanocortin-4 receptor and adiponectin

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Estudi Immunogenètic de les Quimiocines CCL4 i CCL4L: Exemple i Model de la Complexitat de la Superfamília de les Quimiocines

Colobrán, R. (2008) · TDX (Tesis Doctorals en Xarxa)

Personality Genetics and Health in Super-Seniors

Nelson, J. M. T. (2015) · Summit (Simon Fraser University)

Computational Selection and Prioritization of Disease Candidate Genes

Chen, J. (2008) · OhioLink ETD Center (Ohio Library and Information Network)

CANDIDATE GENE STUDY ON NICOTINE DEPENDENCE IN FINNISH SIBPAIRS

Heikkilä, K. (2008) · Jyväskylä University Digital Archive (University of Jyväskylä)

Transcriptional regulation of FEV, a human serotonin neuron developmental control gene

Krueger, K. C. (2009) · OhioLink ETD Center (Ohio Library and Information Network)

Genetic factors influencing bone health in the black South African population

May, A. K. (2012) · University of the Witwatersrand, Johannesburg Institutional Repository on DSpace (University of the Witwatersrand, Johannesburg)

Nutrigenomics: Scientific Discipline

Fogg-Johnson, N., & Kaput, J. (2003)

Comunicación breve Intronic SNP rs3811647 of the human transferrin gene modulates its expression in hepatoma cells

Blanco-Rojo, R., Bayele, H. K., Srai, S. K., & Vaquero, M. P. (2012)

Epigenetic Changes in the Innate Response of Gingival Epithelium

Abdolhosseini, M. (2014) · ScholarlyCommons (University of Pennsylvania)

Genomics of the Liver in Health and Disease

Lazaridis, K. N. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-866-9_8

GENETICS AND CELL BIOLOGY Addictions Biology: Haplotype-Based Analysis for 130 Candidate Genes on a Single Array

Hodgkinson, C. A., Yuan, Q., Shen, P., Heinz, E., Heinz, E., Lobos, E. A., Cubells, J., Ehlers, C. L., Gelernter, J. E., Mann, J., et al. (2008)

EM GENES ASSOCIADOS À APOPTOSE E SUSCEPTIBILIDADE GENÉTICA PARA O CANCRO DA MAMA

Ciências, F. D. (2008)

Análise de polimorfismos das enzimas ciclooxigenase-2 e metilenotetrahidrofolato redutase em pacientes com câncer de esôfago

Zaidan, E. P. (2016) · doi:10.11606/d.5.2016.tde-11042016-110222

The genetic basis for adaptation in natural populations

Lamichhaney, S. (2016) · KTH Publication Database DiVA (KTH Royal Institute of Technology) · doi:10.13140/rg.2.2.17024.84488

Variability of genes involved in inflammatory, immunomodulatory and apoptotic process as a risk factor for head and neck basal cell carcinomas

Kostic, M. (2012) · doi:10.2298/bg20120412kostic

The Nature and Nurture of Wellbeing

Haworth, C. M. A. (2016) · Palgrave Macmillan UK eBooks · doi:10.1057/9781137437327_7

Genetic Epidemiology of Neurologic Disease

Nelson, L. M., Tanner, C. M., Eeden, S. K. V. D., & McGuire, V. M. (2004) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780195133790.003.04

Statistical Approaches to Analysis of Polymorphisms in Multifactorial Conditions

Vandenbroeck, K. (2006) · CRC Press eBooks · doi:10.1201/9781420005325-11

International Efforts on Nutrigenomic Health for Individuals in the Global Community

Kaput, J. (2007) · CRC Press eBooks · doi:10.1201/9781420009170.sec3

Longevity Assurance by Genome Maintenance

Hasty, P., Suh, Y., & Vijg, J. (2013) · CRC Press eBooks · doi:10.1201/b14587-3

Introduction to statistical methods in genome-wide association studies

Yang, C., Li, C., Chung, D., Chen, M., Gelernter, J. E., & Zhao, H. (2015) · Cambridge University Press eBooks · doi:10.1017/cbo9781107337459.005

Reporting and Interpreting Results

Little, J. (2008) · CRC Press eBooks · doi:10.3109/9781420052923-19

Pathogenesis of Periodontal Diseases

Craig, R. G. (2016) · Springer eBooks · doi:10.1007/978-3-662-49699-2_2

Genetic Moderators of Cognitive Decline in the Health and Retirement Study

Runge, S. K. (2016) · Digital Commons - University of South Florida (University of South Florida)

Genetic risk factors for alcohol and nicotine behaviors

Melroy-Greif, W. E. (2015) · CU Scholar (University of Colorado Boulder)

On populations, haplotypes and genome sequencing

Franquin, P. (2012)

Single nucleotide polymorphisms (SNPs) in occupational exposure assessment

Jiang, R. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/vaq3-7v83

GENETIC EPIDEMIOLOGY OF ADIPOSITY AND ABNORMAL GLUCOSE

Vasan, S. K. (2013)

Unravelling the genetic components of late onset Alzheimer's disease.

Hamilton, G. (2005) · OpenGrey (Institut de l'Information Scientifique et Technique)

Polymorphismen in Kandidatengenen der Apoptose als genetische Risikofaktoren für Rheumatoide Arthritis

OESER, C. (2011) · Qucosa (Saxon State and University Library Dresden)

Investigation of genetics and genomics in asthma

Binia, A. (2010) · Spiral (Imperial College London) · doi:10.25560/5593

Towards a Comprehensive Description of the Human Retinal Transcriptome: Identification and Characterization of Differentially Expressed Genes

Würzburg, J.-M.-U. (2003) · Cited by 1

ASSOCIATION BETWEEN NINE IMMUNE SYSTEM GENE POLYMORPHISMS AND TOLERANCE TO ALEUTIAN MINK DISEASE VIRUS INFECTION

Desai, R. (2016) · DalSpace (Dalhousie University)

The Ethical Implications of Emerging Genetic Predictors of Poor Organ Transplant Outcomes

Freeman, M. A. R. (2016) · D-Scholarship@Pitt (University of Pittsburgh)

Effect of indole acetic acid on the in vitro activation and survival of bovine (Bos indicus) preantral follicles.

Blaschi, W., Andrade, E. R., García, J. E., Vilas-Bôas, L. A., Moreira, F., Barreiros, T. R. R., Alfieri, A. F., Alfieri, A. A., & Seneda, M. M. (2010) · Animal Reproduction

SLEEP ALTERATIONS IN MOUSE GENETIC MODELS OF HUMAN DISEASE

Sethi, M. (2016) · UKnowledge (University of Kentucky) · doi:10.13023/etd.2016.522

Einfluss von Keimbahn-Polymorphismen in Genen des TGFβ-Signalwegs und der DNA-Reparatur auf die Strahlenempfindlichkeit Humaner Lymphoblastoider Zellen

Brinkmann, K. M. (2017) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-6154

Análise de polimorfismos da enzima metilenotetrahidrofolato redutase no câncer colorretal

de Souza, D. M. (2017) · doi:10.11606/d.5.2017.tde-03052017-144700

IDENTIFICATION OF NOVEL SLEEP RELATED GENES FROM LARGE SCALE PHENOTYPING EXPERIMENTS IN MICE

Joshi, S. (2017) · UKnowledge (University of Kentucky) · doi:10.13023/etd.2017.159

Genetic Studies of Immunological Diseases in Dogs and Humans

Bianchi, M. (2017) · Uppsala University Publications (Uppsala University)

Functional genomics of the VNN1 gene

Diepeveen, L. A. (2013) · UWA Profiles and Research Repository (UWA)

INTERACTION BETWEEN GENETIC AND OCCUPATIONAL FACTORS IN LUNG CANCER ETIOLOGY.A POPULATION-BASED CASE-CONTROL STUDY.

Matteis, S. D. (2013) · Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano) · doi:10.13130/de-matteis-sara_phd2013-02-07

Leveraging CRISPR/Cas Genome Editing Technology to Identify and Characterize Causal GWAS Variants for Blood Lipids

Raghavan, A. (2017) · Digital Access to Scholarship at Harvard (DASH) (Harvard University)

A Study Evaluating Genetic Trends and Molecular Predisposition to Improved Carcass Quality of Brahman and Brahman Influenced Cattle

Royer, A. (2015) · doi:10.31390/gradschool_theses.3799

Multifactorial Diseases: Asthma Genetics Point the Way Dispatch

Ahmadi, K. R., & Goldstein, D. B. (2002)

Untersuchungen zur Assoziation genetischer Polymorphismen im Gen des Endotoxinrezeptors CD14 mit der transkriptionellen Aktivität

Bregadze, R. (2011) · doi:10.53846/goediss-916

The MAX Statistic is Less Powerful for Genome Wide Association Studies Under Most Alternative Hypotheses

Shifflett, B., Huang, R., & Edland, S. D. (2017) · International Journal of Statistics in Medical Research · doi:10.6000/1929-6029.2017.06.04.2

Genetics of Sedentariness

Huppertz, C., de Geus, E. J. C., & van der Ploeg, H. P. (2017) · Springer series on epidemiology and public health · doi:10.1007/978-3-319-61552-3_27

An Analysis of Genome-Wide Association Studies to Produce Evidence Useful in Guiding Their Reporting and Synthesis

Yurkiewich, A. J. (2012) · uO Research (University of Ottawa) · doi:10.20381/ruor-5448

Association and interplay of genetic and epigenetic variants in smoking behavior

Gupta, R. (2018) · Työväentutkimus Vuosikirja

Association mapping of genes using whole genome polymorphism arrays: Identification of markers of breast cancer susceptibility in Alberta women

Sridharan, M. (2010) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r37d39

Genome-wide search for quantitative trait loci (QTL) and genes for increased growth and improved fatty acid content in salt tolerant tilapia (oreochromis spp.)

Lin, G. (2018) · doi:10.32657/10356/74843

Genetic susceptibility to familial interstitial pneumonia and idiopathic pulmonary fibrosis

Mihalek, A. D., Hunninghake, G. M., & Rosas, I. O. (2015) · doi:10.2217/fmeb2013.14.97

Exploration of SNP-set Interactions in Genome-Wide Association Studies

Alam, S. (2015) · ERA: Education and Research Archive (University of Alberta) · doi:10.7939/r3290k

A study of host genetic determinants of human papillomavirus (HPV) infection, cervical cancer and herpes simplex virus type-2 (HSV-2) infection

Chatterjee, K. (2010) · Open University of Cape Town (University of Cape Town)

Combining genome-wide association studies, polygenic risk scores and SNP-SNP interactions to investigate the genomic architecture of human complex diseases : more than the sum of its parts

Meijsen, J. J. (2018) · ERA

Candidate gene association research on flavones content in hawthorn (Crataegus pinnatifida Bge.)

Zhao, Y., Kia, S., Li-ping, Z., Junpeng, L., & Guo, Y. (2017) · Pakistan Journal of Botany

Exploring the genetic architecture and the chromatin organisation of breast cancer

Leavy, O. C. (2018) · LSHTM Research Online (London School of Hygiene and Tropical Medicine) · doi:10.17037/pubs.04650979

Genetics of Cruciate Ligament Rupture

Baker, L. A., & Muir, P. (2017) · doi:10.1002/9781119261728.ch7

Identification des gènes de susceptibilité à l'asthme à l'aide d'un criblage génomique par association en utilisant des pools d'ADN

Bérubé, J. (2014)

Genetic Variants Associated with the Development of Type 2 Diabetes: Approaches to Their Identification

Stepanova, A. V., Kulebyakin, K. Y., Kochegura, T. N., Shestakova, M. V., & Va, T. (2019) · Annals of the Russian academy of medical sciences · doi:10.15690/vramn1037

Determining the role of the IL2 pathway in susceptibility to juvenile idiopathic arthritis

Taylor, C. J. (2018) · Research Explorer (The University of Manchester)

Genomic and transcriptomic investigations into the feed efficiency phenotype of beef cattle

Higgins, M. G. (2019) · ARAN (University of Galway Research Repository) (Ollscoil na Gaillimhe – University of Galway) · doi:10.13025/16278

Fear learning and extinction

Lonsdorf, T. B. (2019) · Oxford University Press eBooks · doi:10.1093/oso/9780198793014.003.0009

Modifying effects of oxidative stress and DNA repair variants on physical activity and breast cancer risk

McCullough, L. E. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/5z8r-t602

Integrating behavior, hormones and genes associated with the primate HPA-axis

Gutleb, D. R. (2019) · eDiss (Georg-August-Universität Göttingen) · doi:10.53846/goediss-7382

Dose-Finding Designs for Phase I Clinical Trials in Oncology and Use of Selective Phenotypying to Increase Power of Genetic Association Studies

Wang, Y. (2019) · Carolina Digital Repository (University of North Carolina at Chapel Hill) · doi:10.17615/3kcn-qr75

Identification of a genetic contribution to Meniere's disease

Campbell, C. A. (2010) · doi:10.17077/etd.xozz58vv

Exploring the application of psychiatric genetic counselling within the UK.

Spencer-Tansley, R. E. (2016) · Bournemouth University Research Online (Bournemouth University)

Genetic Exploration of Hereditary Immune Diseases

Tian, C. (2018) · doi:10.21007/etd.cghs.2018.0463

Current progress and future direction in the genetics of PTSD: Focus on the development and contributions of the PGC-PTSD working group

Junglen, A. G., Sheerin, C. M., Delahanty, D. L., Hauser, M. A., Lori, A., Morey, R. A., Nievergelt, C. M., Nugent, N. R., Sebat, J. L., Smith, A. K., et al. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-813176-3.00023-7

MORPHOGENETIC CHARACTERIZATION OF WHEAT GERMPLASM FOR DROUGHT TOLERANCE

Muhammad, I. (2015)

Genetics and Aetiology of Atopic Dermatitis

Rodríguez, E., & Weidinger, S. (2019) · Wiley eBooks · doi:10.1002/9781119142812.ch14

Aetiology of Hip Dysplasia: Genetic and Environmental Factors

Thiagarajah, S., Grammatopoulos, G. A., & Wilkinson, J. M. (2020) · Springer eBooks · doi:10.1007/978-3-030-33358-4_1

Mind-reading receptors: The role of the vasopressin receptor 1a gene (AVPR1A) in human empathy, social interaction and health

Morse, A. R. (2019) · ANU Open Research (Australian National University) · doi:10.25911/5f58afa619d23

LOCALIZING GENETIC ELEMENTS ASSOCIATED WITH REPRODUCTIVE PERFORMANCE IN MINK USING A SEQUENCE-BASED SNP PANEL

Konwar, C. (2014) · DalSpace (Dalhousie University)

Epidemiologic Considerations in Complex Disease Genetics: Figure 1.Preprint

Gallacher, J. (2011) · Cold Spring Harbor Protocols · doi:10.1101/pdb.top067512

Association study designs for complex diseases

Cardon, L. R., & Bell, J. I. (2001) · Nature Reviews Genetics · doi:10.1038/35052543 · Cited by 1,395

Genetic Approaches to Studying Common Diseases and Complex Traits

Hirschhorn, J. N. (2005) · Pediatric Research · doi:10.1203/01.pdr.0000159574.98964.87 · Cited by 96

A QUANTITATIVE ANALYSIS OF DISCREPANCIES BETWEEN CANDIDATE GENE AND GENOME-WIDE STUDIES OF COMPLEX TRAITS AND RELATED ENDOPHENOTYPES

Border, R., Johnson, E. C., Sullivan, P. F., Berley, N., & Keller, M. C. (2019) · European Neuropsychopharmacology · doi:10.1016/j.euroneuro.2017.08.121

Genetic association studies.

Austin, M. A., Psaty, B. M., & Schwartz, S. (2013) · CABI eBooks · doi:10.1079/9781780641812.0068