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Genetic Predisposition to Disease [MeSH]
(63)
Humans [MeSH]
(61)
Female [MeSH]
(30)
Male [MeSH]
(29)
Polymorphism, Single Nucleotide [MeSH]
(20)
Article
(14)
Mutation [MeSH]
(11)
Genotype [MeSH]
(11)
Phenotype [MeSH]
(10)
Risk Factors [MeSH]
(6)
Publikationstyp
Artikel
(63)
Erscheinungsjahr
2022
(1)
2021
(36)
2020
(25)
2019
(1)
Institution
Leibniz-Institut für Alternsforschung
(2)
Hessische Stiftung Friedens- und Konfliktforschung
(1)
63 Treffer
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Kurzansicht
E-Jahr
Zugriff
Typ
Operations
Multifaceted Microcephaly-Related Gene MCPH1
2022 .
Kristofova, Martina
|
Ori, Alessandro
|
Wang, Zhao-Qi
2022
http://purl.org/ontology/bibo/Article
Need for psychiatric phenotyping in patients with rare genetic disorders
2021 .
Degenhardt, Franziska
|
Gradl-Dietsch, Gertraud
|
Hebebrand, Johannes
2021
http://purl.org/ontology/bibo/Article
Human genetic variant E756del in the ion channel PIEZO1 not associated with protection from severe malaria in a large Ghanaian study
2021 .
Thye, Thorsten
|
Evans, Jennifer A.
|
Ruge, Gerd
|
Loag, Wibke
|
Ansong, Daniel
|
Agbenyega, Tsiri
|
Horstmann, Rolf D.
|
May, Jürgen
|
Schuldt, Kathrin
2021
http://purl.org/ontology/bibo/Article
Effective identification of cancer predisposition syndromes in children with cancer employing a questionnaire
2021 .
Schwermer, Miriam
|
Behnert, Astrid
|
Dörgeloh, Beate
|
Ripperger, Tim
|
Kratz, Christian
2021
http://purl.org/ontology/bibo/Article
Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family
2021 .
Carrion-Castillo, Amaia
|
B. Estruch, Sara
|
Maassen, Ben
|
Franke, Barbara
|
Francks, Clyde
|
Fisher, Simon
2021
http://purl.org/ontology/bibo/Article
Hormone replacement therapy in BRCA mutation carriers and risk of ovarian, endometrial, and breast cancer: a systematic review
2021 .
Huber, D.
|
Seitz, S.
|
Kast, K.
|
Emons, G.
|
Ortmann, Olaf
2021
http://purl.org/ontology/bibo/Article
SWI/SNF-deficient undifferentiated/rhabdoid carcinoma of the gallbladder carrying a POLE mutation in a 30-year-old woman: a case report
2021 .
Gerber, Tiemo S.
|
Agaimy, Abbas
|
Hartmann, Arndt
|
Habekost, Michael
|
Roth, Wilfried
|
Stenzinger, Albrecht
|
Schirmacher, Peter
|
Straub, Beate K.
2021
http://purl.org/ontology/bibo/Article
Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies
2021 .
Decker, Melanie
|
Lammens, Tim
|
Ferster, Alina
|
Erlacher, Miriam
|
Yoshimi, Ayami
|
Niemeyer, Charlotte
|
Ernst, Martijn P. T.
|
Raaijmakers, Marc H. G. P.
|
Duployez, Nicolas
|
Flaum, Andreas
|
Steinemann, Doris
|
Schlegelberger, Brigitte
|
Illig, Thomas
|
Ripperger, Tim
2021
http://purl.org/ontology/bibo/Article
Genetic factors influencing a neurobiological substrate for psychiatric disorders
2021 .
Andlauer, Till
|
Mühleisen, Thomas W
|
Hoffstaedter, Felix
|
Teumer, Alexander
|
Wittfeld, Katharina
|
Teuber, Anja
|
Reinbold, Céline S.
|
Grotegerd, Dominik
|
Bülow, Robin
|
Caspers, Svenja
|
Dannlowski, Udo
|
Herms, Stefan
|
Hoffmann, Per
|
Kircher, Tilo
|
Minnerup, Heike
|
Moebus, Susanne
|
Nenadić, Igor
|
Teismann, Henning
|
Völker, Uwe
|
Etkin, Amit
|
Berger, Klaus
|
Grabe, Hans J
|
Nöthen, Markus M.
|
Amunts, Katrin
|
Eickhoff, Simon B.
|
Sämann, Philipp G.
|
Müller-Myhsok, Bertram
|
Cichon, Sven
2021
http://purl.org/ontology/bibo/Article
Novel bi-allelic variants expand the SPTBN4-related genetic and phenotypic spectrum
2021 .
Buelow, Markus
|
Süßmuth, David
|
Smith, Laurie D.
|
Aryani, Omid
|
CASTIGLIONI, CLAUDIA
|
Stenzel, Werner
|
Bertini, Enrico
|
Schuelke, Markus
|
Knierim, Ellen
2021
http://purl.org/ontology/bibo/Article
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