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1
المؤلفون: Kathrin A. Giehl, M.P. Birch, Markus M. Nöthen, Rachid Tazi-Ahnini, Andrew G. Messenger, Regina C. Betz, Silke Redler, Dmitriy Drichel, Stefan Herms, Tim Becker, Helmut H. Wolff, Felix F. Brockschmidt, Markus Böhm, Melanie Refke, Gerhard Lutz, Rudolf Kruse, K. Dobson, Nadine Kluck
المصدر: British Journal of Dermatology. 166:1314-1318
مصطلحات موضوعية: Genetics, Candidate gene, Genetic predisposition, Case-control study, medicine, SNP, Male-pattern baldness, Locus (genetics), Single-nucleotide polymorphism, Dermatology, Allele, Biology, medicine.disease
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2
المؤلفون: Felix F. Brockschmidt, Rachid Tazi-Ahnini, Markus M. Nöthen, Hans Wolff, Kathrin A. Giehl, Nadine Kluck, Mary P. Birch, Silke Redler, Melanie Refke, K. Dobson, Regina C. Betz, Andrew G. Messenger, Tim Becker, Markus Böhm, Dmitriy Drichel, Roland Kruse, Gerhard Lutz
المصدر: Experimental dermatology 21(5), 390-393 (2012). doi:10.1111/j.1600-0625.2012.01469.x
مصطلحات موضوعية: medicine.medical_specialty, SRD5A2 protein, human, genetics [3-Oxo-5-alpha-Steroid 4-Dehydrogenase], Dermatology, Biology, Biochemistry, genetics [Estrogen Receptor beta], 3-Oxo-5-alpha-Steroid 4-Dehydrogenase, Germany, Internal medicine, Progesterone receptor, medicine, Humans, Estrogen Receptor beta, ddc:610, SRD5A1 protein, human, Receptor, estrogen receptor alpha, human, Molecular Biology, Alleles, genetics [Alopecia], Estrogen Receptor alpha, Genetic Variation, Membrane Proteins, Alopecia, medicine.disease, genetics [Genetic Variation], United Kingdom, ethnology [Alopecia], genetics [Membrane Proteins], Endocrinology, Hair loss, Receptors, Estrogen, Hormone receptor, Sex steroid, Case-Control Studies, SRD5A2, genetics [Receptors, Progesterone], Female, genetics [Estrogen Receptor alpha], genetics [Receptors, Estrogen], Receptors, Progesterone, Estrogen receptor alpha, Hormone
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3
المؤلفون: Lutz Priebe, Margrieta A. Alblas, Rami Abou Jamra, Nadine Kluck, Sibylle Eigelshoven, Susanne Moebus, Felix F. Brockschmidt, Stefanie Heilmann, Raimund Erbel, Tim Becker, Christine Herold, Holger Fröhlich, Stephen B. Harrap, Axel M. Hillmer, Christian Meesters, Karl-Heinz Jöckel, Rudolf Kruse, B. Lippke, Justine A. Ellis, Franziska Degenhardt, Sandra Hanneken, Markus M. Nöthen, Johannes Schumacher
المصدر: British Journal of Dermatology. 165:1293-1302
مصطلحات موضوعية: Genetics, Candidate gene, Hair cycle, HDAC9, medicine, Male-pattern baldness, Genome-wide association study, Single-nucleotide polymorphism, Locus (genetics), Dermatology, Biology, medicine.disease, Gene
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4
المؤلفون: Andreas Ziegler, Andreas Warnke, Gerd Schulte-Körne, Myriam Peyrard-Janvid, Nadine Kluck, Heidi Anthoni, Faten Dahdouh, Malou Manthey, Helmut Remschmidt, Juha Kere, Axel M. Hillmer, Marco Zucchelli, Sven Cichon, Markus M. Nöthen, Ellen Plume, Jutta Hülsmann, Peter Propping, Cecilia M. Lindgren, Johannes Schumacher, Inke R. König
المصدر: The American Journal of Human Genetics. 78(1):52-62
مصطلحات موضوعية: Central Nervous System, Genetic Markers, Linkage disequilibrium, Genotype, Molecular Sequence Data, Nerve Tissue Proteins, Locus (genetics), Biology, Linkage Disequilibrium, Genetic determinism, Dyslexia, 03 medical and health sciences, 0302 clinical medicine, DCDC2, Germany, medicine, Genetics, Humans, Genetic Predisposition to Disease, Genetics(clinical), Genetics (clinical), DNA Primers, 030304 developmental biology, 0303 health sciences, Base Sequence, Haplotype, Sequence Analysis, DNA, Articles, Blotting, Northern, medicine.disease, Doublecortin, Gene Components, Phenotype, Haplotypes, biology.protein, Chromosomes, Human, Pair 6, Microtubule-Associated Proteins, 030217 neurology & neurosurgery
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5
المؤلفون: Nadine Kluck, J Winantea, Peter Propping, Markus M. Nöthen, Jan Freudenberg, Sven Cichon, Yun Freudenberg-Hua, Michael Brüss
المصدر: The Pharmacogenomics Journal. 5:183-192
مصطلحات موضوعية: Bipolar Disorder, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, Receptors, G-Protein-Coupled, Databases, Genetic, Genetics, Humans, SNP, Genetic variability, Gene, Genotyping, Alleles, Pharmacology, Reverse Transcriptase Polymerase Chain Reaction, Haplotype, Genetic Variation, DNA, SNP genotyping, Haplotypes, Pharmacogenetics, Data Interpretation, Statistical, Schizophrenia, Molecular Medicine, Human genome, Software, Central Nervous System Agents, Signal Transduction
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6
المؤلفون: Rudolf Kruse, K. Dobson, Tim Becker, Markus M. Nöthen, Helmut H. Wolff, Gerhard Lutz, Nadine Kluck, Dmitriy Drichel, Felix F. Brockschmidt, Kathrin A. Giehl, Rachid Tazi-Ahnini, Regina C. Betz, Andrew G. Messenger, Silke Redler, M.P. Birch
المصدر: British Journal of Dermatology. 165:703-705
مصطلحات موضوعية: medicine.medical_specialty, biology, business.industry, MEDLINE, Dermatology, medicine.disease, Bioinformatics, Hair loss, Endocrinology, Text mining, Internal medicine, medicine, biology.protein, Aromatase, business, Gene
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7
المؤلفون: Peter Propping, Martin Scheer, Michael Knapp, Stefan Herms, Carlotta Baluardo, Sandra Barth, Thomas Meitinger, Bettina Blaumeiser, Simone Pötzsch, Markus M. Nöthen, Jessica Becker, Bert Braumann, Per Hoffmann, Thomas F. Wienker, Sven Cichon, Melissa Ferrian, Peter A. Mossey, Stefan Schreiber, Michele Rubini, Nadine Kluck, Michael Steffens, Régine P.M. Steegers-Theunissen, Michael Krawczak, Nilma Almeida de Assis, Anna Paul, Stefanie Birnbaum, Heiko Reutter, Gül Schmidt, Manuel Mattheisen, Kerstin U. Ludwig, Rudolf H. Reich, Carola Lauster, Hans Erich Wichmann, Taofik Al Chawa, Elisabeth Mangold, Susanne Moebus, Franz Josef Kramer, Alexander Hemprich
المساهمون: Obstetrics & Gynecology
المصدر: Nature Genetics, 42(1), 24-26. Nature Publishing Group
Nature geneticsمصطلحات موضوعية: Genome-wide association study, Cleft Lip, Medizin, Locus (genetics), Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Cleft lip and palate, Genotype, Genetics, Humans, GWAS, Genetic Predisposition to Disease, genetics, birth defects, NOG, VAX1, 030304 developmental biology, 0303 health sciences, 030305 genetics & heredity, Chromosome Mapping, Cleft Palate, Relative risk, nonsyndromic cleft lip, Susceptibility locus, IRF6, Human medicine, Congenital disease
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8
المؤلفون: Sven Cichon, Nadine Kluck, Manuel Mattheisen, Thomas F. Wienker, Sandra Barth, Elisabeth Mangold, Nikolaos Daratsianos, Anna Paul, Jessica Becker, Taofik AlChawa, Simone Pötzsch, Peter A. Mossey, Mary L. Marazita, Margrieta A. Alblas, Terri H. Beaty, Markus M. Nöthen, Rudolf H. Reich, Stefanie Nowak, Entessar Nasser, Bert Braumann, Bettina Blaumeiser, Franz Josef Kramer, Alan F. Scott, Ingo Ruczinski, Kerstin U. Ludwig, Thomas Kreusch, Christoph Lange, Carola Lauster, Jeffrey C. Murray, Per Hoffmann, Ruth Herberz, Régine P.M. Steegers-Theunissen, Alexander Hemprich, Heiko Reutter, Peter Propping, Michael Knapp, Michele Rubini, Stefan Herms, Anne C. Böhmer
المساهمون: Obstetrics & Gynecology, Epidemiology
المصدر: Nature Genetics, 44(9), 968-971. Nature Publishing Group
Nature geneticsمصطلحات موضوعية: Adult, Male, Parents, Cleft Lip, Biology, Polymorphism, Single Nucleotide, Genome, Article, Genetica, labiopalatoschisi, malformazioni congenite, GWAS, 03 medical and health sciences, 0302 clinical medicine, Risk Factors, Genetics, Humans, Genetic Predisposition to Disease, Child, 030304 developmental biology, Genetic association, 0303 health sciences, Syndrome, 030206 dentistry, Confidence interval, Cleft Palate, Relative risk, Female, IRF6, Human medicine, Genetic risk factor, Genome-Wide Association Study
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9
المؤلفون: Heiko Reutter, Stefanie Nowak, Elisabeth Mangold, Markus M. Nöthen, Bert Braumann, Kerstin U. Ludwig, Nadine Kluck, Carola Lauster, Nilma Almeida de Assis, Per Hoffmann, Thomas F. Wienker, Rudolf H. Reich, Alexander Hemprich, Jennifer Vollmer, Michael Knapp, Franz-Josef Kramer, Stefanie Heilmann
المصدر: International journal of pediatric otorhinolaryngology. 75(1)
مصطلحات موضوعية: Male, Candidate gene, Genotype, Cleft Lip, SUMO-1 Protein, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, 03 medical and health sciences, Humans, Genetic Predisposition to Disease, Europe, Eastern, Allele, Genotyping, Alleles, Genetic Association Studies, 030304 developmental biology, Genetic association, Genetics, 0303 health sciences, Incidence, 030305 genetics & heredity, Haplotype, Case-control study, Genetic Variation, General Medicine, Pedigree, Cleft Palate, Otorhinolaryngology, Case-Control Studies, Pediatrics, Perinatology and Child Health, Female
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10
المؤلفون: Markus M. Nöthen, Peter Propping, Nadine Kluck, Jan Freudenberg, Yun Freudenberg-Hua, Sven Cichon
المصدر: Genome research
مصطلحات موضوعية: Nonsynonymous substitution, Candidate gene, Biology, Polymorphism, Single Nucleotide, Gene Frequency, Central Nervous System Diseases, Untranslated Regions, Genetic variation, Databases, Genetic, Genetics, Humans, Genetic Testing, Letters, Allele, Transversion, Codon, Allele frequency, Genetics (clinical), Alleles, Transition (genetics), Genetic Variation, Minor allele frequency, Genes, Population Surveillance, DNA, Intergenic
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f2902598542ce291855392550e56e7ca
https://hdl.handle.net/10067/428980151162165141
Full Text via ClinicalKey