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Dr. rer. nat. Arif Bülent Ekici
List of publications:
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Institute of Human Genetics
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(7)
Publications
(289)
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Journal article
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Genetic variants in the glucocorticoid pathway genes and birth weight (2020)
Schneider M, Hübner T, Pretscher J, Goecke TW, Schwitulla J, Häberle L, Kornhuber J, et al.
Journal article
Variants in SCAF4 Cause a Neurodevelopmental Disorder and Are Associated with Impaired mRNA Processing (2020)
Fliedner A, Kirchner P, Wiesener A, van de Beek I, Waisfisz Q, van Haelst M, Scott DA, et al.
Journal article
Mendelian randomization analyses suggest a role for cholesterol in the development of endometrial cancer (2020)
Kho PF, Amant F, Annibali D, Ashton K, Attia J, Auer PL, Beckmann M, et al.
Journal article
Rare Loss-of-Function Mutation in SERPINA3 in Generalized Pustular Psoriasis (2020)
Frey S, Sticht H, Wilsmann-Theis D, Gerschütz A, Wolf K, Löhr S, Haskamp S, et al.
Journal article
Genetic studies of urinary metabolites illuminate mechanisms of detoxification and excretion in humans (2020)
Schlosser P, Li Y, Sekula P, Raffler J, Grundner-Culemann F, Pietzner M, Cheng Y, et al.
Journal article
The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer (2019)
Figlioli G, Bogliolo M, Catucci I, Caleca L, Lasheras SV, Pujol R, Kiiski JI, et al.
Journal article
Two truncating variants in FANCC and breast cancer risk (2019)
Dork T, Peterlongo P, Mannermaa A, Bolla MK, Wang Q, Dennis J, Ahearn T, et al.
Journal article
In Vivo Protein Complementation Demonstrates Presynaptic α-Synuclein Oligomerization and Age-Dependent Accumulation of 8–16-mer Oligomer Species (2019)
Kiechle M, von Einem B, Höfs L, Voehringer P, Grozdanov V, Markx D, Parlato R, et al.
Journal article
CRISPR/Cas9-mediated knock-out of krasG12D mutated pancreatic cancer cell lines (2019)
Lentsch E, Li L, Pfeffer S, Ekici AB, Taher L, Pilarsky C, Grützmann R
Journal article
Prenatal diagnosis of HNF1B-associated renal cysts: Is there a need to differentiate intragenic variants from 17q12 microdeletion syndrome? (2019)
Vasileiou G, Hoyer J, Thiel C, Schaefer JT, Zapke M, Krumbiegel M, Kraus C, et al.
Journal article
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