Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: NEUROD2[original query] |
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HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer. British journal of cancer 2006 Dec 95 (12): 1689-95. Benusiglio P R, Pharoah P D, Smith P L, Lesueur F, Conroy D, Luben R N, Dew G, Jordan C, Dunning A, Easton D F, Ponder B A |
Lack of association between SNPs in the NEUROD2 gene and alcohol dependence in a German patient sample. Psychiatry research 2011 May 187 (1-2): 220-3. Zill Peter, Preuss Ulrich W, Koller Gabrielle, Bondy Brigitta, Soyka Micha |
Associations of NEUROD2 polymorphisms and change of cognitive dysfunctions in schizophrenia and schizoaffective disorder after eight weeks of antipsychotic treatment. Cognitive neuropsychiatry 2017 May 1-18. Spellmann Ilja, Riedel Michael, Städtler Julia, Zill Peter, Obermeier Michael, Cerovecki Anja, Dehning Sandra, Schennach Rebecca, Epple Maria, Opgen-Rhein Markus, Müller Norbert, Bondy Brigitta, Möller Hans-Jürgen, Musil Richa |
Genome-wide association study identifies novel recessive genetic variants for high TGs in an Arab population.
Journal of lipid research 2018 Aug . Hebbar Prashantha, Nizam Rasheeba, Melhem Motasem, Alkayal Fadi, Elkum Naser, John Sumi Elsa, Tuomilehto Jaakko, Alsmadi Osama, Thanaraj Thangavel Alphon |
Expansion of NEUROD2 phenotypes to include developmental delay without seizures. American journal of medical genetics. Part A 2021 1 185 (4): 1076-1080. Mis Emily K, Sega Annalisa G, Signer Rebecca H, Cartwright Tracy, Ji Weizhen, Martinez-Agosto Julian A, Nelson Stanley F, Palmer Christina G S, Lee Hane, Mitzelfelt Thomas, Konstantino Monica, , Jeffries Lauren, Khokha Mustafa K, Marco Elysa, Martin Martin G, Lakhani Saquib |
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