Ruppert, Ann‐Kathrin
57  results:
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4

Homozygous mutation in TXNRD1 is associated with genetic ge..:

Kudin, Alexei P. ; Baron, Gregor ; Zsurka, Gábor...
Free Radical Biology and Medicine.  106 (2017)  - p. 270-277 , 2017
 
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9

Linkage Evidence for a Two-Locus Inheritance of LQT-Associa..:

Prüss, Harald ; Gessner, Guido ; Heinemann, Stefan H...
info:eu-repo/semantics/altIdentifier/doi/10.3389/fneur.2019.00648.  , 2019
 
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11

No evidence for a BRD2 promoter hypermethylation in blood l..:

Schulz, Herbert ; Ruppert, Ann-Kathrin ; Zara, Federico...
Schulz , H , Ruppert , A-K , Zara , F , Madia , F , Iacomino , M , S Vari , M , Balagura , G , Minetti , C , Striano , P , Bianchi , A , Marini , C , Guerrini , R , Weber , Y G , Becker , F , Lerche , H , Kapser , C , Schankin , C J , Kunz , W S , Møller , R S , Oliver , K L , Bellows , S T , Mullen , S A , Berkovic , S F , Scheffer , I E , Caglayan , H , Ozbek , U , Hoffmann , P , Schramm , S , Tsortouktzidis , D , Becker , A J & Sander , T 2019 , ' No evidence for a BRD2 promoter hypermethylation in blood leukocytes of Europeans with juvenile myoclonic epilepsy ' , Epilepsia , vol. 60 , no. 5 , pp. e31-e36 . https://doi.org/10.1111/epi.14657.  , 2019
 
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13

Analysis of shared heritability in common disorders of the ..:

Anttila, Verneri ; Sullivan, Brenda ; Finucane, Hilary...
info:eu-repo/semantics/altIdentifier/doi/10.1126/science.aap8757.  , 2018
 
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14

Analysis of shared heritability in common disorders of the ..:

Anttila, Verneri ; Sullivan, Brenda ; Finucane, Hilary...
info:eu-repo/semantics/altIdentifier/doi/10.1126/science.aap8757.  , 2018
 
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