A Novel Multilocus Genetic Model Can Predict Muscle Fibers Composition

Borisov, O, Kulemin, N, Ahmetov, I, and Generozov, E (2018).

In: Advances in Intelligent Systems and Computing, vol. 663, pp. 164–168, Springer (ISBN: 9783319678450).

Rank miRNA: A web tool for identifying polymorphisms altering miRNA target sites

Beretta, S, Maj, C, and Merelli, I (2017).

Procedia Computer Science, 108(C):1125–1134.

An analysis of six pharmacogenomic association studies revealed significant correlation between allele frequency and corresponding odds ratios

Borisov, O and Generozov, E (2017).

Clinical Therapeutics, 39 (8 Supp(8):e89.

Study of Microrna-Related Single-Nucleotide Polymorphisms in Major Depressive Disorder

Maffioletti, E, Congiu, C, Bonvicini, C, Maj, C, Minelli, A, Bortolomasi, M, Maina, G, Bocchio-Chiavetto, L, and Gennarelli, M (2017).

In: European Neuropsychopharmacology, vol. 27, pp. S212—-S213, ELSEVIER SCIENCE BV PO BOX 211, 1000 AE AMSTERDAM, NETHERLANDS.

Study of the in vitro modulation exerted by the antidepressant drug escitalopram on the expression of candidate microRNAs and their target genes.

Maffioletti, E, Salvi, A, Conde, I, Maj, C, Gennarelli, M, De Petro, G, and Bocchio-Chiavetto, L (2017).

Molecular and cellular neurosciences, 85:220–225.

RNA-Sequencing of Bipolar Disorder Patients Lymphoblastoid Cell Lines Implicates A Novel Neurotrophic Factor In The Efficacy of Lithium As Mood Stabilizing Drug

Milanesi, E, Voinsky, I, Hadar, A, Maj, C, Kelsoe, JR, Shekhtman, T, Zandi, P, Goes, F, Potash, JB, Greshovits, M, Gilad, S, Gennarelli, M, Schulze, TG, and Gurwitz, D (2017).

European Neuropsychopharmacology, 27:S391–S392.

RNA sequencing of bipolar disorder lymphoblastoid cell lines implicates the neurotrophic factor HRP-3 in lithium's clinical efficacy

Milanesi, E, Voinsky, I, Hadar, A, Srouji, A, Maj, C, Shekhtman, T, Gershovits, M, Gilad, S, Chillotti, C, Squassina, A, Potash, JB, Schulze, TG, Goes, FS, Zandi, P, Kelsoe, JR, and Gurwitz, D (2017).

World Journal of Biological Psychiatry:1–13.

Mutations in MYO1H cause a recessive form of central hypoventilation with autonomic dysfunction

Spielmann, M, Hernandez-Miranda, LR, Ceccherini, I, Weese-Mayer, DE, Kragesteen, BK, Harabula, I, Krawitz, P, Birchmeier, C, Leonard, N, and Mundlos, S (2017).

Journal of Medical Genetics, 54(11):754–761.

A Novel de novo FZD2 Mutation in a Patient with Autosomal Dominant Omodysplasia

Türkmen, S, Spielmann, M, Güneş, N, Knaus, A, Flöttmann, R, Mundlos, S, and Tüysüz, B (2017).

Molecular Syndromology, 8(6):318–324.

Chromatin-remodeling factor SMARCD2 regulates transcriptional networks controlling differentiation of neutrophil granulocytes

Nature Genetics, 49(5):742–752.

Witzel, M, Petersheim, D, Fan, Y, Bahrami, E, Racek, T, Rohlfs, M, Puchałka, J, Mertes, C, Gagneur, J, Ziegenhain, C, Enard, W, Stray-Pedersen, A, Arkwright, PD, Abboud, MR, Pazhakh, V, Lieschke, GJ, Krawitz, PM, Dahlhoff, M, Schneider, MR, Wolf, E, Horny, HP, Schmidt, H, Schäffer, AA, and Klein, C (2017).

Reduced cell surface levels of GPI-linked markers in a new case with PIGG loss of function

Zhao, JJ, Halvardson, J, Knaus, A, Georgii-Hemming, P, Baeck, P, Krawitz, PM, Thuresson, AC, and Feuk, L (2017).

Human Mutation, 38(10):1394–1401.

Estimating the correlation between the accuracy of simulation-based genetic risk modelling and its principal prediction parameters interrelationship

Borisov, O, Babalyan, K, Kulemin, N, and Generozov, E ().

Investigative Ophthalmology & Visual Science, 63(7):1161--1161.

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