المؤلفون: Mertens, R., Graupera, M., Gerhardt, H., Bersano, A., Tournier-Lasserve, E., Mensah, M. A., Mundlos, S., Vajkoczy, Peter

المصدر: http://lobid.org/resources/99370675589506441Test#!, 13(1):25-45.

مصطلحات موضوعية: Stroke, Adenosine Triphosphatases/genetics [MeSH], Genetics, Humans [MeSH], RNF 213, Review Article, Moyamoya Disease/genetics [MeSH], Moyamoya disease, Ubiquitin-Protein Ligases/genetics [MeSH], 17q25, Genetic Predisposition to Disease/genetics [MeSH], Moyamoya Disease/diagnostic imaging [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6444154Test; https://doi.org/10.1007/s12975-021-00940-2Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766392Test/

الإتاحة: https://doi.org/10.1007/s12975-021-00940-2Test
https://repository.publisso.de/resource/frl:6444154Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8766392Test/

المؤلفون: Steixner-Kumar, Agnes A., Daguano Gastaldi, Vinicius, Seidel, Jan, Rosenberger, Albert, Begemann, Martin, Ehrenreich, Hannelore

المصدر: http://lobid.org/resources/99370675519006441Test#!, 26(7):3211-3222.

مصطلحات موضوعية: Article, Genetics, Adult [MeSH], Humans [MeSH], Schizophrenia [MeSH], Genetic Association Studies [MeSH], Schizophrenia, Addiction, Polymorphism, Single Nucleotide/genetics [MeSH], Genetic Predisposition to Disease/genetics [MeSH], Genome-Wide Association Study [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6443766Test; https://doi.org/10.1038/s41380-021-01069-2Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505259Test/

الإتاحة: https://doi.org/10.1038/s41380-021-01069-2Test
https://repository.publisso.de/resource/frl:6443766Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8505259Test/

المؤلفون: Winter, Greta, Kirschner-Schwabe, Renate, Groeneveld-Krentz, Stefanie, Escherich, Gabriele, Möricke, Anja, von Stackelberg, Arend, Stanulla, Martin, Bailey, Simon, Richter, Lisa, Steinemann, Doris, Ripperger, Tim, Escudero, Adela, Farah, Roula, Lohi, Olli, Wadt, Karin, Jongmans, Marjolijn, van Engelen, Nienke, Eckert, Cornelia, Kratz, Christian

المصدر: http://lobid.org/resources/99370672770606441Test#!, 35(5):1475-1479.

مصطلحات موضوعية: Adolescent [MeSH], Female [MeSH], Letter, Humans [MeSH], Li-Fraumeni Syndrome/genetics [MeSH], Risk factors, Acute lymphocytic leukaemia, Genetics research, Male [MeSH], Precursor Cell Lymphoblastic Leukemia-Lymphoma/genetics [MeSH], Child [MeSH], Genetic Predisposition to Disease/genetics [MeSH], Child, Preschool [MeSH], Germ-Line Mutation/genetics [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6443850Test; https://doi.org/10.1038/s41375-021-01163-yTest; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102191Test/

الإتاحة: https://doi.org/10.1038/s41375-021-01163-yTest
https://repository.publisso.de/resource/frl:6443850Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8102191Test/

المؤلفون: Rupprecht, Christian, Rupprecht, Rainer, Rammes, Gerhard

المصدر: http://lobid.org/resources/99370678531206441Test#!, 271(5):809-812.

مصطلحات موضوعية: Brain/metabolism [MeSH], Protein Structure, Secondary [MeSH], Complement C1q/metabolism [MeSH], Amyloid beta-Peptides/metabolism [MeSH], Humans [MeSH], Psychiatry, Complement C1q/genetics [MeSH], Alzheimer Disease/metabolism [MeSH], Aging/physiology [MeSH], Neurosciences, Editorial, Genetic Predisposition to Disease/genetics [MeSH]

العلاقة: https://repository.publisso.de/resource/frl:6447286Test; https://doi.org/10.1007/s00406-021-01273-9Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236034Test/

الإتاحة: https://doi.org/10.1007/s00406-021-01273-9Test
https://repository.publisso.de/resource/frl:6447286Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8236034Test/

المؤلفون: Schneider, Susanne A., Hizli, Baccara, Alcalay, Roy N.

المصدر: http://lobid.org/resources/99370674841006441Test#!, 17(4):1378-1392.

مصطلحات موضوعية: TORC1 inhibitor, Deep Brain Stimulation/trends [MeSH], SNCA, GBA, Genetic Parkinson’s disease, Deep Brain Stimulation/methods [MeSH], alpha-Synuclein/genetics [MeSH], clinical trial, Parkinsonian Disorders/therapy [MeSH], Genetic Predisposition to Disease/genetics [MeSH], small molecule compounds, Mutation/genetics [MeSH], Genetic Predisposition to Disease/epidemiology [MeSH], Humans [MeSH], Precision Medicine/methods [MeSH], kinase inhibitor, ambroxol, Genetic Therapy/trends [MeSH], Precision Medicine/trends [MeSH], Leucine-Rich Repeat Serine-Threonine Protein Kinase-2/genetics [MeSH], Clinical Trials as Topic/methods [MeSH], Parkinsonian Disorders/genetics [MeSH], Parkinsonian Disorders/epidemiology [MeSH], Review, Genetic Therapy/methods [MeSH], LRRK2, Venglustat

العلاقة: https://repository.publisso.de/resource/frl:6471320Test; https://doi.org/10.1007/s13311-020-00920-8Test; https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483040Test/

الإتاحة: https://doi.org/10.1007/s13311-020-00920-8Test
https://repository.publisso.de/resource/frl:6471320Test
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7483040Test/

المؤلفون: Hohmann, Sarah, Häge, Alexander, Millenet, Sabina, Banaschewski, Tobias

المصدر: http://lobid.org/resources/99370674607406441Test#!, 50(3):203-217.

مصطلحات موضوعية: ADHD, Genetik, Pleiotropie, Attention Deficit Disorder with Hyperactivity/diagnosis [MeSH], Multifactorial Inheritance/genetics [MeSH], Übersichtsarbeit, Humans [MeSH], genetics, polygenetische Risikoscores, Komorbidität, ADHS, Attention Deficit Disorder with Hyperactivity/genetics [MeSH], comorbidities, Attention Deficit Disorder with Hyperactivity/epidemiology [MeSH], Genome-Wide Association Study [MeSH], Comorbidity [MeSH], pleiotropy, comorbidity, Genetic Predisposition to Disease/genetics [MeSH], polygenic risk scores

العلاقة: https://repository.publisso.de/resource/frl:6475190Test; https://doi.org/10.1024/1422-4917/a000868Test

الإتاحة: https://doi.org/10.1024/1422-4917/a000868Test
https://repository.publisso.de/resource/frl:6475190Test