المؤلفون: J. Gheuens, J. J. Martin, Michael Mullan, Gerd Multhaup, N.G. Irving, Antoon Vandenberghe, Hugh Gurling, W. Van Hul, A. Genthe, John Hardy, A. Wehnert, A. Barton, M. Salbaum, Bernhard Horsthemke, Marc Bruyland, H Backhovens, S. J. Richards, Konrad Beyreuther, C. Van Broeckhoven, A. Holland, Robert Williamson, Colin L. Masters, Peter Raeymaekers, Patrick Cras

المصدر: Nature

مصطلحات موضوعية: Adult, Male, Amyloid, Chromosomes, Human, Pair 21, Genetic Linkage, Locus (genetics), Disease, Biology, Alzheimer Disease, Genetic linkage, medicine, Humans, Senile plaques, Protein Precursors, Genetics, Amyloid beta-Peptides, Polymorphism, Genetic, Multidisciplinary, Molecular pathology, Chromosome Mapping, medicine.disease, Pedigree, Genes, Female, Alzheimer's disease, Chromosome 21, Engineering sciences. Technology

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f73777dee0f802153a1b26c3c1a5967aTest
https://doi.org/10.1038/329153a0Test

المؤلفون: Jeroen Aerssens, Peter Raeymaekers, Hugo Geerts, Frank Konings, Sean Lilienfeld, Wim Parys

المصدر: Dementia and Geriatric Cognitive Disorders. 12:69-77

مصطلحات موضوعية: Apolipoprotein E, medicine.medical_specialty, education.field_of_study, Mini–Mental State Examination, medicine.diagnostic_test, Cognitive Neuroscience, Cognitive disorder, Population, medicine.disease, Psychiatry and Mental health, chemistry.chemical_compound, chemistry, Internal medicine, Sabeluzole, medicine, Galantamine, Dementia, Geriatrics and Gerontology, Alzheimer's disease, Psychology, education, Psychiatry, medicine.drug

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::5c4e8d71dbd32f1ddd19434422db4b4aTest
https://doi.org/10.1159/000051238Test

المؤلفون: Christiane Hilger, Olivier Lipp, D. Dikeos, Alessandro Serretti, Julien Mendlewicz, Isabelle Massat, Manfred Ackenheil, Luc Staner, Sybille Fuchshuber, Sylvie Blairy, Fabio Macciardi, Daniel Souery, Radka Kaneva, Miro Jakovljević, Christine Van Broeckhoven, V. Milanova, Lilijana Oruc, Peter Raeymaekers, Georgio Papadimitriou, G.R. Verheyen

المصدر: American Journal of Medical Genetics. 96:136-140

مصطلحات موضوعية: Genetics, Candidate gene, Genotype, medicine, Genetic predisposition, Bipolar disorder, Allele, Biology, medicine.disease, Allele frequency, Genetics (clinical), Genetic determinism, Genotype frequency

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9fc87838986ef8aa417571fa456b1419Test
https://doi.org/10.1002Test/(sici)1096-8628(20000403)96:2<136::aid-ajmg2>3.0.co;2-s

المؤلفون: Sandra M. Villafuerte, Christine Van Broeckhoven, Peter Raeymaekers, G.R. Verheyen, Daniel Souery, Jurgen Del-Favero, Julien Mendlewicz

المصدر: European Journal of Human Genetics. 7:427-434

مصطلحات موضوعية: Genetic Markers, Genetics, Yeast artificial chromosome, Bipolar Disorder, Contig, Genetic Linkage, Haplotype, Biology, Contig Mapping, Haplotypes, Chromosome (genetic algorithm), Genetic distance, Chromosome 18, Humans, Family, Allele, Chromosomes, Human, Pair 18, Chromosomes, Artificial, Yeast, Gene, Genetics (clinical)

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f8e6b87b20a50121abb30ae9ff29255Test
https://doi.org/10.1038/sj.ejhg.5200318Test

المؤلفون: Roderick H. J. Houwen, Nelson B. Freimer, Jenneke Juyn, Kathleen Blankenship, Siamak Baharloo, Lodewijk A. Sandkuijl, Peter Raeymaekers

المصدر: Nature Genetics. 8:380-386

مصطلحات موضوعية: Male, Genetics, Linkage disequilibrium, Genotype, Haplotype, Benign Recurrent Intrahepatic Cholestasis, Chromosome Mapping, Locus (genetics), Cholestasis, Intrahepatic, Biology, Genome, Pedigree, Haplotypes, Gene mapping, Recurrence, Chromosome 18, Humans, Female, Chromosomes, Human, Pair 18, Gene, Probability

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::14bbf814fa46f95f361bbc7d812352c5Test
https://doi.org/10.1038/ng1294-380Test

المؤلفون: Vincent Timmerman, Jean-Jacques Martin, Chantal Ceuterick, Eva Nelis, Ludo Muylle, Peter Raeymaekers, Peter De Jonghe, Christine Van Broeckhoven

المصدر: Journal of the neurological sciences

مصطلحات موضوعية: Genetic Markers, Male, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Pathology, Charcot-Marie-Tooth Disease, Genetic linkage, Humans, Medicine, Genes, Dominant, Motor Neurons, Genetics, business.industry, Cytogenetics, Chromosome, Spinal muscular atrophies, medicine.disease, SMA, Autosomal dominant form, Pedigree, nervous system diseases, Neurology, Chromosomes, Human, Pair 1, Chromosomes, Human, Pair 5, Female, Neurology (clinical), Lod Score, Hereditary Sensory and Motor Neuropathy, business, Chromosomes, Human, Pair 19, Motor neuropathy, Chromosomes, Human, Pair 17

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6620ced9e3cea0a05beb6b56b4e2a99Test
https://doi.org/10.1016/0022-510xTest(92)90091-x

المؤلفون: Guy P. Mannaerts, Peter Marynen, Paul P. Van Veldhoven, Peter Raeymaekers, Marc Fransen

المصدر: Genomics. 30:366-368

مصطلحات موضوعية: Genetics, Chromosomes, Human, Pair 12, Base Sequence, Peroxisome-Targeting Signal 1 Receptor, medicine.diagnostic_test, Molecular Sequence Data, Chromosome Mapping, Receptors, Cytoplasmic and Nuclear, Hybrid Cells, Biology, Gene mutation, Molecular biology, Loss of heterozygosity, Gene mapping, Cosmid, medicine, Humans, Gene, Peroxisomal targeting signal, Alleles, In Situ Hybridization, Fluorescence, Chromosome 12, DNA Primers, Fluorescence in situ hybridization

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ca78c1eebc7dd2f297742e1fb644886Test
https://doi.org/10.1006/geno.1995.0032Test

المؤلفون: Ilya, Chumakov, Marta, Blumenfeld, Oxana, Guerassimenko, Laurent, Cavarec, Marta, Palicio, Hadi, Abderrahim, Lydie, Bougueleret, Caroline, Barry, Hiroaki, Tanaka, Philippe, La Rosa, Anne, Puech, Nadia, Tahri, Annick, Cohen-Akenine, Sylvain, Delabrosse, Sébastien, Lissarrague, Françoise-Pascaline, Picard, Karelle, Maurice, Laurent, Essioux, Philippe, Millasseau, Pascale, Grel, Virginie, Debailleul, Anne-Marie, Simon, Dominique, Caterina, Isabelle, Dufaure, Kattayoun, Malekzadeh, Maria, Belova, Jian-Jian, Luan, Michel, Bouillot, Jean-Luc, Sambucy, Gwenael, Primas, Martial, Saumier, Nadia, Boubkiri, Sandrine, Martin-Saumier, Myriam, Nasroune, Hélène, Peixoto, Arnaud, Delaye, Virginie, Pinchot, Mariam, Bastucci, Sophie, Guillou, Magali, Chevillon, Ricardo, Sainz-Fuertes, Said, Meguenni, Joan, Aurich-Costa, Dorra, Cherif, Anne, Gimalac, Cornelia, Van Duijn, Denis, Gauvreau, Gail, Ouellette, Isabel, Fortier, John, Raelson, Tatiana, Sherbatich, Nadejda, Riazanskaia, Evgeny, Rogaev, Peter, Raeymaekers, Jeroen, Aerssens, Frank, Konings, Walter, Luyten, Fabio, Macciardi, Pak C, Sham, Richard E, Straub, Daniel R, Weinberger, Nadine, Cohen, Daniel, Cohen, Gail, Ouelette, John, Realson

المساهمون: Epidemiology

المصدر: Proceedings of the National Academy of Sciences of the U.S.A., 99, 13675-13680. National Academy of Sciences

مصطلحات موضوعية: Genetic Markers, D-Amino-Acid Oxidase, Chromosomes, Artificial, Bacterial, Receptor expression, Molecular Sequence Data, Population, Models, Neurological, D-amino acid oxidase, Single-nucleotide polymorphism, In Vitro Techniques, Biology, Polymorphism, Single Nucleotide, Receptors, N-Methyl-D-Aspartate, Two-Hybrid System Techniques, Humans, Amino Acid Sequence, Cloning, Molecular, education, Gene, Peptide sequence, Genetics, education.field_of_study, Multidisciplinary, Chromosomes, Human, Pair 13, Sequence Homology, Amino Acid, Mental Disorders, Chromosome Mapping, Biological Sciences, Molecular biology, Enzyme Activation, Dysbindin, Genetic marker, Case-Control Studies, Commentary, Schizophrenia, Signal Transduction

وصف الملف: application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::83667f3c76d9cca850cd3d8b7c5233eeTest
https://pure.eur.nl/en/publications/0848e3a4-4a47-4286-aca4-f79574228a30Test

المؤلفون: Stephan Claes, Jean-Jacques Cassiman, Koenraad Devriendt, Peter Raeymaekers, Jean-Pierre Fryns, P Volcke, Maureen Holvoet

المصدر: American journal of medical genetics

مصطلحات موضوعية: Genetics, Linkage (software), congenital, hereditary, and neonatal diseases and abnormalities, business.industry, Heterozygote advantage, medicine.disease, Genetic determinism, Developmental disorder, Gene mapping, Genetic linkage, Medicine, business, Gene, Genetics (clinical), X chromosome

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80226b5298351b64d52e12577433981aTest
https://hdl.handle.net/10067/380280151162165141Test

المؤلفون: Toril Fagerheim, Finn Egil Tønnessen, Peter Raeymaekers, Herbert A. Lubs

المصدر: Neuropsychology and Cognition ISBN: 9789401059671

مصطلحات موضوعية: Linkage (software), Genetics, Reading disability, media_common.quotation_subject, Dyslexia, Norwegian, medicine.disease, language.human_language, Spelling, Test (assessment), Developmental psychology, Chromosome 15, Reading (process), medicine, language, Psychology, psychological phenomena and processes, media_common

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::312739bac3d72cfceff890d4a84293aaTest
https://doi.org/10.1007/978-94-011-4667-8_11Test