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1. Analysis of human genetic linkage
by Ott, Jurg
1991, Rev. ed. --, Johns Hopkins series in contemporary medicine and public health., ISBN 0801842573, xxii, 302
Human genetics | Linkage (Genetics)
Book
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2. Analysis of human genetic linkage
by Ott, Jurg
1999, 3rd ed., ISBN 9780801861406, xxiii, 382
Human genetics | Linkage (Genetics)
Book
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3. Analysis of human genetic linkage
by Ott, Jurg
1985, The Johns Hopkins series contemporary medicine and public health, ISBN 0801824850, xii, 223
Human genetics | Linkage (Genetics)
Book
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4. To aggregate or not, that is the question. A commentary on single-nucleotide variant proportion in genes: A new concept to explore major depression based on DNA sequencing data
by Ott, Jurg
Journal of Human Genetics, ISSN 1434-5161, 04/2017, Volume 62, Issue 5, pp. 523 - 523
DISEASE | GENETICS & HEREDITY | Genetic Predisposition to Disease | Polymorphism, Single Nucleotide | High-Throughput Nucleotide Sequencing - methods | Depressive Disorder, Major - genetics | Sequence Analysis, DNA - methods | Humans
Journal Article
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5. Handbook of human genetic linkage
by Terwilliger, Joseph Douglas and Ott, Jurg
1994, ISBN 0801848032, x, 307
Data processing | Linkage (Genetics) | Human genetics | Computer programs
Book
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6. 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 | Index Medicus | Abridged Index Medicus
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7. Full Text OBITUARY: Richard S. Spielman 1946-2009
by Jurg Ott
Nature Genetics, ISSN 1061-4036, 11/2009, Volume 41, Issue 11, p. 1159
  Here, Spielman again showed his interest in characterizing genetic variation, and his productive combination of statistical models with these early genetic... 
Studies | Linguistics | Statistical methods | Biology | Mutation | Population genetics
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8. Full Text Richard S. Spielman 1946-2009
by Ott, Jurg
Nature Genetics, ISSN 1061-4036, 11/2009, Volume 41, Issue 11, pp. 1159 - 1159
College teachers
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9. Full Text Association of genetic loci: Replication or not, that is the question
by Ott, Jurg
Neurology, ISSN 0028-3878, 09/2004, Volume 63, Issue 6, pp. 955 - 958
OBESITY | CLINICAL NEUROLOGY | DISEASE | Humans | False Positive Reactions | Anticonvulsants - pharmacology | Case-Control Studies | Haplotypes - genetics | Chromosome Mapping - standards | Ethnic Groups - genetics | Chromosome Mapping - methods | Publication Bias | Epilepsy - genetics | Reproducibility of Results | Drug Resistance, Multiple - genetics | Gene Frequency | Anticonvulsants - therapeutic use | Genotype | Probability Theory | ATP Binding Cassette Transporter, Subfamily B, Member 1 - genetics | Linkage Disequilibrium | Polymorphism, Genetic | Sample Size | Confounding Factors (Epidemiology) | Publishing - standards | Selection Bias | Epilepsy - drug therapy | Polymorphism, Single Nucleotide | ATP Binding Cassette Transporter, Subfamily B, Member 1 - physiology | Amino Acid Substitution | Index Medicus | Abridged Index Medicus
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10. Full Text Complement Factor H Polymorphism in Age-Related Macular Degeneration
by Robert J. Klein and Caroline Zeiss and Emily Y. Chew and Jen-Yue Tsai and Richard S. Sackler and Chad Haynes and Alice K. Henning and John Paul SanGiovanni and Shrikant M. Mane and Susan T. Mayne and Michael B. Bracken and Frederick L. Ferris and Jurg Ott and Colin Barnstable and Josephine Hoh
Science, ISSN 0036-8075, 4/2005, Volume 308, Issue 5720, pp. 385 - 389
Age-related macular degeneration (AMD) is a major cause of blindness in the elderly. We report a genome-wide screen of 96 cases and 50 controls for... 
Haplotypes | Drusen | Linkage disequilibrium | Genes | Alleles | Medical genetics | P values | Research Articles | Magnetic fields | Chromosomes | Genotypes | EXTENDED FAMILIES | DRUSEN | ACTIVATION | PROJECT | GENOMEWIDE-SCAN | ASSOCIATIONS | PROTEIN | MULTIDISCIPLINARY SCIENCES | DISEASE | REGIONS | SUSCEPTIBILITY LOCI | Oligonucleotide Array Sequence Analysis | Exons | Pigment Epithelium of Eye - immunology | Humans | Male | Case-Control Studies | Aged, 80 and over | Aging | Female | Chromosomes, Human, Pair 1 - genetics | Genetic Predisposition to Disease | Complement Factor H - physiology | Introns | Risk Factors | Histidine - genetics | Genotype | Genetic Markers | Immunity, Innate | Linkage Disequilibrium | Polymorphism, Genetic | Macular Degeneration - genetics | Complement Membrane Attack Complex - analysis | Choroid - immunology | Aged | Polymorphism, Single Nucleotide | Complement Factor H - genetics | Amino Acid Substitution | Complement Factor H - chemistry | Smoking | Proteins | Macular degeneration | Care and treatment | Genomes | Research | Risk factors | Genotype & phenotype | Older people | Polymorphism | Index Medicus
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11. Full Text A14520 The joint effects of cardiovascular disease related SNPs on ischemic stroke
by Liu, Xin and Xu, Ke and Ott, Jurg and Wang, Xingyu
Journal of Hypertension, ISSN 0263-6352, 10/2018, Volume 36 Suppl 3, pp. e71 - e71
OBJECTIVES:Previous studies have revealed multiple common variants associated with known risk factors for cardiovascular disease (CVD). Ischemic stroke (IS)... 
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12. Full Text AprioriGWAS, a New Pattern Mining Strategy for Detecting Genetic Variants Associated with Disease through Interaction Effects
by Zhang, Qingrun and Long, Quan and Ott, Jurg
PLoS Computational Biology, ISSN 1553-734X, 2014, Volume 10, Issue 6, pp. e1003627 - e1003627
Identifying gene-gene interaction is a hot topic in genome wide association studies. Two fundamental challenges are: (1) how to smartly identify combinations... 
COMPLEMENT FACTOR-H | BLOOD-RETINAL BARRIER | RECOGNITION | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | MACULAR DEGENERATION | MISSING HERITABILITY | POLYMORPHISM | BIPOLAR DISORDER | RECEPTORS | EPISTASIS | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Humans | Computational Biology | Databases, Genetic | Logistic Models | Genome-Wide Association Study - statistics & numerical data | Bipolar Disorder - genetics | Linkage Disequilibrium | Genetic Variation | Algorithms | Macular Degeneration - genetics | Epistasis, Genetic | Computer Simulation | Data Mining - statistics & numerical data | Models, Genetic | Complement Factor H - genetics | Genome-wide association studies | Genetic aspects | Disease transmission | Research | Genetic variation | Index Medicus | Macular degeneration | Genotype & phenotype | Bipolar disorder | Genes
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13. Full Text Multilocus association mapping using generalized ridge logistic regression
by Liu, Zhe and Shen, Yuanyuan and Ott, Jurg
BMC Bioinformatics, ISSN 1471-2105, 09/2011, Volume 12, Issue 1, pp. 384 - 384
Background: In genome-wide association studies, it is widely accepted that multilocus methods are more powerful than testing single-nucleotide polymorphisms... 
TRUNCATED PRODUCT | BIOCHEMICAL RESEARCH METHODS | MACULAR DEGENERATION | PATTERNS | POLYMORPHISM | P-VALUES | MODELS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | LASSO | MATHEMATICAL & COMPUTATIONAL BIOLOGY | REGULARIZATION | SELECTION | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Disease - genetics | Humans | Logistic Models | Chromosome Mapping | Polymorphism, Single Nucleotide | Case-Control Studies | Linkage Disequilibrium | Usage | Chromosome mapping | Single nucleotide polymorphisms | Research | Applications software | Computational biology | Studies | Variables | Genomes | Statistical methods | Disease | Advantages | Index Medicus
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14. Full Text Dysfunctional nitric oxide signalling increases risk of myocardial infarction
by Erdmann, Jeanette and Stark, Klaus and Esslinger, Ulrike B and Rumpf, Philipp Moritz and Koesling, Doris and DeWit, Cor and Kaiser, Frank J and Braunholz, Diana and Medack, Anja and Fischer, Marcus and Zimmermann, Martina E and Tennstedt, Stephanie and Graf, Elisabeth and Eck, Sebastian and Aherrahrou, Zouhair and Nahrstaedt, Janja and Willenborg, Christina and Bruse, Petra and Brænne, Ingrid and Nöthen, Markus M and Hofmann, Per and Braund, Peter S and Mergia, Evanthia and Reinhard, Wibke and Burgdorf, Christof and Schreiber, Stefan and Balmforth, Anthony J and Hall, Alistair S and Bertram, Lars and Steinhagen-Thiessen, Elisabeth and Li, Shu-Chen and März, Winfried and Reilly, Muredach and Kathiresan, Sekar and McPherson, Ruth and Walter, Ulrich and Ott, Jurg and Samani, Nilesh J and Strom, Tim M and Meitinger, Thomas and Hengstenberg, Christian and Schunkert, Heribert and CARDIoGRAM
Nature, ISSN 0028-0836, 2013, Volume 504, Issue 7480, pp. 432 - 436
Myocardial infarction, a leading cause of death intheWesternworld(1), usually occurs when the fibrous cap overlying an atherosclerotic plaque in a coronary... 
SUSCEPTIBILITY LOCI | ADULTS | SOLUBLE GUANYLATE-CYCLASE | MULTIDISCIPLINARY SCIENCES | CORONARY-ARTERY-DISEASE | GENOME-WIDE ASSOCIATION | Myocardial Infarction - genetics | Receptors, Cytoplasmic and Nuclear - deficiency | Humans | Disease Susceptibility - metabolism | Male | Vasodilation | Chaperonin Containing TCP-1 - genetics | HEK293 Cells | Female | Myocardial Infarction - physiopathology | Chaperonin Containing TCP-1 - metabolism | Genetic Predisposition to Disease | Reproducibility of Results | Signal Transduction | Solubility | Guanylate Cyclase - metabolism | Soluble Guanylyl Cyclase | Receptors, Cytoplasmic and Nuclear - genetics | Myocardial Infarction - metabolism | Mutation - genetics | Exome - genetics | Guanylate Cyclase - deficiency | Thrombosis - metabolism | Animals | Cyclic GMP - metabolism | Pedigree | Platelet Activation | Guanylate Cyclase - genetics | Mice | Nitric Oxide - metabolism | Receptors, Cytoplasmic and Nuclear - metabolism | Proteins | Cardiovascular disease | Genomes | Mutation | Mortality | Blood clots | Index Medicus
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15. HDR: A statistical two-step approach successfully identifies disease genes in autosomal recessive families
by Imai, Atsuko and Kohda, Masakazu and Nakaya, Akihiro and Sakata, Yasushi and Murayama, Kei and Ohtake, Akira and Lathrop, Mark and Okazaki, Yasushi and Ott, Jurg
Journal of Human Genetics, ISSN 1434-5161, 11/2016, Volume 61, Issue 11, pp. 959 - 963
In the search for sequence variants underlying disease, commonly applied filtering steps usually result in a number of candidate variants that cannot further... 
GENOMEWIDE SCANS | HOMOZYGOSITY | DNA | LENGTH | GENETICS & HEREDITY | HAMMING DISTANCE | TRUE | MUTATIONS | SEQUENCING DATA | FALSE-POSITIVE PEAKS | CHILDREN | Computational Biology - methods | Genetic Predisposition to Disease | Pedigree | Humans | Genetic Association Studies - methods | Genotype | Software | Genes, Recessive | Case-Control Studies | Genetic Linkage
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16. Full Text Distribution and characterization of regulatory elements in the human genome
by Majewski, Jacek and Ott, Jurg
Genome Research, ISSN 1088-9051, 12/2002, Volume 12, Issue 12, pp. 1827 - 1836
The regulation of transcription and subsequent gene splicing are crucial to correct gene expression. Although a number of regulatory sequences involved in both... 
SITE SELECTION | BIOCHEMISTRY & MOLECULAR BIOLOGY | CPG METHYLATION | HUMAN GENES | PRE-MESSENGER-RNA | COMPUTATIONAL ANALYSIS | EXONIC SPLICING ENHANCERS | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | INTRONS | IN-VIVO | GENETICS & HEREDITY | VERTEBRATES | MUTATIONS | Introns - genetics | Humans | Databases, Genetic | Exons - genetics | Short Interspersed Nucleotide Elements - genetics | Regulatory Sequences, Nucleic Acid - genetics | Microsatellite Repeats - genetics | Chromosome Mapping - methods | DNA Transposable Elements - genetics | Polymorphism, Single Nucleotide - genetics | Models, Genetic | Base Composition - genetics | Genome, Human | Mutagenesis | Introns | Analysis | Physiological aspects | Genomes | Genetic aspects | Research | Genetic regulation | Gene expression | Methods | Index Medicus | Letter
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17. Full Text Increased OPRM1 DNA methylation in lymphocytes of methadone-maintained former heroin addicts
by Nielsen, David A and Yuferov, Vadim and Hamon, Sara and Jackson, Colin and Ho, Ann and Ott, Jurg and Kreek, Mary Jeanne
Neuropsychopharmacology, ISSN 0893-133X, 2009, Volume 34, Issue 4, pp. 867 - 873
The mu-opioid receptor is the site of action of opiates and opioids. We examined whether there are differences in cytosine : guanine (CpG) dinucleotide... 
CpG | Methadone | Addiction | Gene | Methylation | Heroin | heroin | HYPERMETHYLATION | gene | MESSENGER-RNA EXPRESSION | PSYCHIATRY | addiction | COCAINE | NEUROSCIENCES | MU-OPIOID RECEPTOR | methylation | GENE-EXPRESSION | EPIGENETIC REGULATION | PHARMACOLOGY & PHARMACY | PROMOTER | methadone | UP-REGULATION | CPG ISLANDS | ALCOHOL DEPENDENCE | Lymphocytes - metabolism | Promoter Regions, Genetic | European Continental Ancestry Group - genetics | Heroin Dependence - drug therapy | Receptors, Opioid, mu - metabolism | Humans | Methadone - therapeutic use | Molecular Sequence Data | Male | Sequence Analysis, DNA | DNA Methylation | Base Sequence | CpG Islands | Female | Software | Receptors, Opioid, mu - genetics | Heroin Dependence - genetics | Index Medicus
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18. Full Text The BRCA1-interacting helicase BRIP1 is deficient in Fanconi anemia
by Levran, Orna and Milton, Kelly L and Henry, Rashida T and Neveling, Kornelia and Ott, Jurg and Attwooll, Claire and Rio, Paula and Schindler, Detlev and Petrini, John and Batish, Sat Dev and Auerbach, Arleen D and Velleuer, Eunike and Kalb, Reinhard and Barral, Sandra and Hanenberg, Helmut
Nature Genetics, ISSN 1061-4036, 09/2005, Volume 37, Issue 9, pp. 931 - 933
Seven Fanconi anemia-associated proteins (FANCA, FANCB, FANCC, FANCE, FANCF, FANCG and FANCL) form a nuclear Fanconi anemia core complex that activates the... 
PROTEIN | BRCA1 | DNA-REPAIR | BACH1 | GENETICS & HEREDITY | RNA Helicases - metabolism | Fanconi Anemia Complementation Group D2 Protein | Humans | Cell Cycle Proteins - metabolism | Ubiquitin - metabolism | Male | Nuclear Proteins - metabolism | DNA-Binding Proteins - genetics | Mutation - genetics | Fanconi Anemia Complementation Group Proteins | Blotting, Western | DNA-Binding Proteins - metabolism | Chromosomes, Human, Pair 17 | Pedigree | Cell Cycle Proteins - genetics | Fanconi Anemia Complementation Group C Protein | Female | RNA Helicases - genetics | Fanconi Anemia - genetics | Polymorphism, Single Nucleotide | Nuclear Proteins - genetics | Cell Nucleus | Microsatellite Repeats | Polymerase chain reaction | Usage | BRCA mutations | Genetic aspects | Research | Health aspects | Risk factors | Fanconi's anemia | Index Medicus
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19. Full Text AprioriGWAS, a New Pattern Mining Strategy for Detecting Genetic Variants Associated with Disease through Interaction Effects
: e1003627
by Qingrun Zhang and Quan Long and Jurg Ott
PLoS Computational Biology, ISSN 1553-734X, 06/2014, Volume 10, Issue 6
  Identifying gene-gene interaction is a hot topic in genome wide association studies. Two fundamental challenges are: (1) how to smartly identify combinations... 
Macular degeneration | Genotype & phenotype | Algorithms | Genes | Bipolar disorder
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