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1. Full Text The whole side of it--an interview with Neil Risch by Jane Gitschier
by Risch, Neil
PLoS genetics, ISSN 1553-7390, 07/2005, Volume 1, Issue 1, p. e14
Genetics, Population | Genetic Predisposition to Disease | History, 21st Century | Molecular Epidemiology | United States
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2. Full Text The whole side of it--an interview with Neil Risch. Interview by Jane Gitschier
by Risch, Neil
PLoS genetics, ISSN 1553-7390, 07/2005, Volume 1, Issue 1, p. 3
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3. Full Text Presidential Address: All in the Family, or "Gee, Our Old LaSalle Ran Great".sup.1
by Risch, Neil
American Journal of Human Genetics, ISSN 0002-9297, 03/2016, Volume 98, Issue 3, p. 407
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.ajhg.2016.02.009 Byline: Neil Risch Author Affiliation: (2)... 
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4. Full Text Presidential Address: All in the Family, or “Gee, Our Old LaSalle Ran Great”
by Risch, Neil
The American Journal of Human Genetics, ISSN 0002-9297, 03/2016, Volume 98, Issue 3, pp. 407 - 416
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5. Full Text Presidential Address: All in the Family, or “Gee, Our Old LaSalle Ran Great” 1
by Risch, Neil
The American Journal of Human Genetics, ISSN 0002-9297, 03/2016, Volume 98, Issue 3, pp. 407 - 416
ASHG Awards and Addresses
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6. Full Text Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
by Botstein, David and Botstein, David and Risch, Neil and Risch, Neil
Nature Genetics, ISSN 1061-4036, 03/2003, Volume 33, Issue 3S, pp. 228 - 237
The past two decades have witnessed an explosion in the identification, largely by positional cloning, of genes associated with mendelian diseases. The roughly... 
MARIE-TOOTH-DISEASE | HUMAN GENOME | SEQUENCE VARIATION | GENETICS & HEREDITY | FRAGMENT LENGTH POLYMORPHISMS | LINKAGE-DISEQUILIBRIUM | FOUNDER POPULATIONS | FANCONI-ANEMIA | HUNTINGTONS-DISEASE | SINGLE-NUCLEOTIDE POLYMORPHISMS | CYSTIC-FIBROSIS GENE | History, 21st Century | History, 20th Century | Humans | Genetic Diseases, Inborn - genetics | Genotype | Chromosome Mapping | Genomics - history | Genetic Diseases, Inborn - history | Linkage Disequilibrium | Phenotype | Alleles | Cloning, Molecular | Polymorphism, Single Nucleotide | Mutation | Genomics - trends | Physiological aspects | Research | DNA | Human genetics
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7. Full Text Presidential Address: All in the Family, or "Gee, Our Old LaSalle Ran Great"
by Risch, N
AMERICAN JOURNAL OF HUMAN GENETICS, ISSN 0002-9297, 03/2016, Volume 98, Issue 3, pp. 407 - 416
GENETICS & HEREDITY | HEALTH | Societies, Medical - organization & administration | Demography | Genome, Human | Humans
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8. Full Text Searching for genetic determinants in the new millennium
by Risch, Neil J
Nature, ISSN 0028-0836, 06/2000, Volume 405, Issue 6788, pp. 847 - 856
Human genetics is now at a critical juncture. The molecular methods used successfully to identify the genes underlying rare mendelian syndromes are failing to... 
COMPLEX HUMAN-DISEASES | RELATIVE POWER | DEPENDENT DIABETES-MELLITUS | MAPPING GENES | CASE-CONTROL DESIGNS | LINKAGE DISEQUILIBRIUM | MULTIDISCIPLINARY SCIENCES | MARKERS | LOCI | ALLELIC ASSOCIATION | SINGLE-NUCLEOTIDE POLYMORPHISMS | Biotechnology | Genetic Predisposition to Disease | Humans | Computational Biology | Genetic Diseases, Inborn - genetics | Genetics, Medical - trends | Genome, Human | Genetics | Medical disorders | Genes | Genomics
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9. Full Text Dissecting Racial and Ethnic Differences
by Risch, Neil
The New England Journal of Medicine, ISSN 0028-4793, 01/2006, Volume 354, Issue 4, pp. 408 - 411
It is well known that disease does not affect the population equally. Assessing variation in the rates of disease according to demographic factors such as sex... 
GENETIC-STRUCTURE | MEDICINE, GENERAL & INTERNAL | CYP2A6 | METABOLISM | NICOTINE | RACE | POPULATIONS | HEALTH DISPARITIES | Lung Neoplasms - genetics | Smoking - adverse effects | Lung Neoplasms - ethnology | United States - epidemiology | European Continental Ancestry Group - genetics | Gene Frequency | Humans | Hispanic Americans | African Americans - genetics | Hawaii | Male | Risk | Incidence | Smoking - ethnology | Asian Americans - genetics | Lung Neoplasms - etiology | Female | Oceanic Ancestry Group
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10. Full Text Structured mating: Patterns and implications
by Sebro, Ronnie and Peloso, Gina M and Dupuis, Josée and Risch, Neil J
PLoS Genetics, ISSN 1553-7390, 04/2017, Volume 13, Issue 4, p. e1006655
Genetic similarity of spouses can reflect factors influencing mate choice, such as physical/behavioral characteristics, and patterns of social endogamy. Spouse... 
HEART | HUMAN HEIGHT | POPULATION STRATIFICATION | GENETICS & HEREDITY | SPOUSAL CONCORDANCE | EUROPEAN AMERICANS | TRAITS | SELECTION | ASSOCIATION | ANCESTRY | HERITABILITY | European Continental Ancestry Group - genetics | Genome-Wide Association Study | Phenotype | Humans | Female | Genotype | Male | Spouses | Polymorphism, Single Nucleotide | Genome, Human | Jews - genetics | Linkage Disequilibrium | Single nucleotide polymorphisms | Research | Health aspects | Chromosomes | Genomics | Married people | Heart | Assortative mating | Clines | Linkage disequilibrium | Principal components analysis | Cardiovascular disease | Genomes | Single-nucleotide polymorphism | Mate selection | Mating | Studies | Progeny | Genotype & phenotype | Population | Heritability | Health risk assessment | Public health | Polymorphism
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11. Full Text Interaction Between the Serotonin Transporter Gene (5-HTTLPR), Stressful Life Events, and Risk of Depression: A Meta-analysis
by Risch, Neil and Herrell, Richard and Lehner, Thomas and Liang, Kung-Yee and Eaves, Lindon and Hoh, Josephine and Griem, Andrea and Kovacs, Maria and Ott, Jurg and Merikangas, Kathleen Ries
JAMA, ISSN 0098-7484, 06/2009, Volume 301, Issue 23, pp. 2462 - 2471
CONTEXT Substantial resources are being devoted to identify candidate genes for complex mental and behavioral disorders through inclusion of environmental... 
REGION 5-HTTLPR | SOCIAL SUPPORTS | MEDICINE, GENERAL & INTERNAL | POLYMORPHISM 5-HTTLPR | PSYCHIATRIC-DISORDERS | PROMOTER POLYMORPHISM | MALTREATED CHILDREN | HUMAN-DISEASES | MAJOR DEPRESSION | THREATENING EXPERIENCES | X ENVIRONMENT INTERACTION | Stress, Psychological - genetics | Serotonin Plasma Membrane Transport Proteins - genetics | Depressive Disorder, Major - genetics | Humans | Life Change Events | Risk Factors | Female | Genotype | Male | Studies | Genotype & phenotype | Mental depression | Stress | Meta-analysis | Depressive Disorders | Neurotransmitters | Multiple Traumatic Events | Predisposition | Survivors | Genetic Markers | Meta Analysis | Females | Males | Stressors
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12. Full Text The Beaker phenomenon and the genomic transformation of northwest Europe
by Olalde, Iñigo and Brace, Selina and Allentoft, Morten E and Armit, Ian and Kristiansen, Kristian and Booth, Thomas and Rohland, Nadin and Mallick, Swapan and Szécsényi-Nagy, Anna and Mittnik, Alissa and Altena, Eveline and Lipson, Mark and Lazaridis, Iosif and Harper, Thomas K and Patterson, Nick and Broomandkhoshbacht, Nasreen and Diekmann, Yoan and Faltyskova, Zuzana and Fernandes, Daniel and Ferry, Matthew and Harney, Eadaoin and De Knijff, Peter and Michel, Megan and Oppenheimer, Jonas and Stewardson, Kristin and Barclay, Alistair and Alt, Kurt Werner and Liesau, Corina and Rios, Patricia and Blasco, Concepcion and Miguel, Jorge Vega and Garcia, Roberto Menduina and Fernandez, Azucena Aviles and Banffy, Eszter and Bernabo-Brea, Maria and Billoin, David and Bonsall, Clive and Bonsall, Laura and Allen, Tim and Buster, Lindsey and Carver, Sophie and Navarro, Laura Castells and Craig, Oliver E and Cook, Gordon T and Cunliffe, Barry and Denaire, Anthony and Dinwiddy, Kirsten Egging and Dodwell, Natasha and Ernee, Michal and Evans, Christopher and Kucharik, Milan and Farre, Joan Frances and Fowler, Chris and Gazenbeek, Michiel and Pena, Rafael Garrido and Haber-Uriarte, Maria and Haduch, Elzbieta and Hey, Gill and Jowett, Nick and Knowles, Timothy and Massy, Ken and Pfrengle, Saskia and Lefranc, Philippe and Lemercier, Olivier and Lefebvre, Arnaud and Martinez, Cesar Heras and Olmo, Virginia Galera and Ramirez, Ana Bastida and Maurandi, Joaquin Lomba and Majo, Tona and McKinley, Jacqueline I and McSweeney, Kathleen and Mende, Balazs Gusztav and Mod, Alessandra and Kulcsar, Gabriella and Kiss, Viktoria and Czene, Andras and Patay, Robert and Endrodi, Anna and Kohler, Kitti and Hajdu, Tamas and Szeniczey, Tamas and Dani, Janos and Bernert, Zsolt and Hoole, Maya and Cheronet, Olivia and Keating, Denise and Veleminsky, Petr and Dobe, Miroslav and Candilio, Francesca and Brown, Fraser and Fernandez, Raul Flores and Herrero-Corral, Ana-Mercedes and Tusa, Sebastiano and Carnieri, Emiliano and Lentini, Luigi and Valenti, Antonella and Zanini, Alessandro and Waddington, Clive and Delibes, German and ... and Institutionen för historiska studier and Humanistiska fakulteten and Göteborgs universitet and Gothenburg University and Faculty of Arts and Department of Historical Studies
Nature, ISSN 0028-0836, 03/2018, Volume 555, Issue 7695, pp. 190 - 196
From around 2750 to 2500 bc, Bell Beaker pottery became widespread across western and central Europe, before it disappeared between 2200 and 1800 bc. The... 
MIGRATION | EARLY FARMERS | ORIGIN | DNA | PERSISTENCE | MULTIDISCIPLINARY SCIENCES | SEQUENCE | DIVERSITY | ANCIENT BONES | ADMIXTURE | HISTORY | Haplotypes | Genetics, Population | History, Ancient | Europe | Gene Pool | Genomics | Humans | Male | Cultural Evolution - history | Genome, Human - genetics | Human Migration - history | Chromosomes, Human, Y - genetics | DNA, Ancient | Spatio-Temporal Analysis | Europeans | Genetic aspects | Genetic transformation | Research | Transformation | Migration | Gene pool | Principal components analysis | Genomes | Ceramics | Neolithic | Artifacts | Archaeology | S gene | Artefacts | Pottery | Stone Age | Copper | Bioinformatics | Deoxyribonucleic acid--DNA | Geography | Environmental Engineering | Humanities and Social Sciences | Biodiversity and Ecology | Environmental and Society | Environmental Sciences | Global Changes | Arkeologi | admixture | 1st farmers | Science & Technology - Other Topics | history | Genetik | ancient bones | dna | migration | Genetics | persistence | eurasia | populations | early farmers
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13. Full Text Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation
by Hoffmann, Thomas J and Ehret, Georg B and Nandakumar, Priyanka and Ranatunga, Dilrini and Schaefer, Catherine and Kwok, Pui-Yan and Iribarren, Carlos and Chakravarti, Aravinda and Risch, Neil
Nature Genetics, ISSN 1061-4036, 01/2017, Volume 49, Issue 1, pp. 54 - 64
Longitudinal electronic health records on 99,785 Genetic Epidemiology Research on Adult Health and Aging (GERA) cohort individuals provided 1,342,814 systolic... 
MEAN ARTERIAL | INDIVIDUALS | METAANALYSIS | VARIANTS | GENETICS & HEREDITY | COMMON | GENETIC-LOCI | AFRICAN | PULSE PRESSURE | TRAITS | HYPERTENSION | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Prevalence | Blood Pressure - genetics | Humans | Middle Aged | Genetic Loci - genetics | Male | Phenotype | Ethnic Groups - genetics | Polymorphism, Single Nucleotide - genetics | Adult | Female | Hypertension - epidemiology | Hypertension - genetics | Electronic Health Records | Longitudinal Studies | Cohort Studies | Medical records | Genome-wide association studies | Blood pressure | Management | Analysis | Studies | Body mass index | Genotype & phenotype | Genealogy | Hispanic Americans | African Americans | Genomes | Research | Electronic health records | Age | blood pressure | electronic health records | hypertension | genome-wide association study
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14. Full Text The Future of Genetic Studies of Complex Human Diseases
by Neil Risch and Kathleen Merikangas
Science, ISSN 0036-8075, 9/1996, Volume 273, Issue 5281, pp. 1516 - 1517
Risch and Merikangas argue that the method that linkage analysis has limited power to detect genes of modest effect, but association studies, which utilize... 
Alleles | Medical genetics | Parents | Disease risk | Genetic loci | Perspectives | Genetic diseases | Alzheimers disease | Epidemiology | Human genetics | Siblings | TRAITS | MULTIDISCIPLINARY SCIENCES | Genetic Predisposition to Disease | Humans | Genetic Diseases, Inborn - genetics | Probability | Genotype | Heterozygote | Genetic Techniques | Genome, Human | Genetic Linkage | Polymorphism, Genetic | Genetic disorders | Research | Methods | Genetics | Statistical analysis | Disease | Genes
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15. Full Text Gene-set meta-analysis of lung cancer identifies pathway related to systemic lupus erythematosus
by Rosenberger, Albert and Sohns, Melanie and Friedrichs, Stefanie and Hung, Rayjean J and Fehringer, Gord and McLaughlin, John and Amos, Christopher I and Brennan, Paul and Risch, Angela and Brüske, Irene and Caporaso, Neil E and Landi, Maria Teresa and Christiani, David C and Wei, Yongyue and Bickeböller, Heike
PLoS ONE, ISSN 1932-6203, 03/2017, Volume 12, Issue 3, p. e0173339
Introduction Gene-set analysis (GSA) is an approach using the results of single-marker genome-wide association studies when investigating pathways as a whole... 
RISK-FACTORS | POLYMORPHISMS | VARIANTS | INFLAMMATION | MULTIDISCIPLINARY SCIENCES | POOLED ANALYSIS | SUSCEPTIBILITY LOCUS | NEVER-SMOKERS | 15Q25 | DNA-REPAIR | ASSOCIATION | Lung Neoplasms - genetics | Computational Biology - methods | Gene Expression | Genetic Predisposition to Disease | Genome-Wide Association Study | Signal Transduction | Humans | Lupus Erythematosus, Systemic - metabolism | Chromosome Mapping | Gene Expression Profiling | Case-Control Studies | Lupus Erythematosus, Systemic - genetics | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Genetic aspects | Systemic lupus erythematosus | Analysis | Lung cancer | Risk factors | Genes | Linkage disequilibrium | Encyclopedias | Genomes | Epidemiology | DNA repair | Consortia | Pathways | Cell cycle | Genetics | Public health | Deoxyribonucleic acid--DNA | Lupus | Medical research | Rheumatic diseases | Chromosome 6 | Lung carcinoma | Studies | Pleiotropy | Chronic conditions | Information processing | Autoimmune diseases | Cancer | Deoxyribonucleic acid | DNA
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