November 2017
New publication: Cost-effective screening of DNMT3A coding sequence identifies somatic mutation in pediatric T-cell acute lymphoblastic leukemia.
Szarzyńska-Zawadzka B, Kosmalska M, Sędek Ł, Sonsala A, Twardoch M, Kowalczyk JR, Szczepański T, Witt M, Dawidowska M
Eur J Haematol, 2017, 99 (6): 514-519, IF-2.653, MNiSW-20.
New publication: Genetic factors influencingthe reduction of central corneal thickness in disorders affecting the eye.
Świerkowska J, Gajęcka M
Ophthalmic Genetics, 2017, 38 (6): 501-510, IF-1.277, MNiSW-20
New publication: Longrange PCR-based next-generation sequencing in pharmacokinetics and pharmacodynamics study of propofol among patients under general anaesthesia.
Zakerska-Banaszak O, Skrzypczak-Zielińska M, Tamowicz B, Mikstacki A, Walczak M, Prendecki M, Doroszewska J, Pollak A, Lechowicz U, Oldak M, Huminska-Lisowska K, Molinska-Glura M, Szalata M, Słomski R
Scientific Report, 2017, Nov 13; 7(1):15399. doi: 10.1038/s41598-017-15657-2, IF-4.259, MNiSW-40
New publication: New EPCAM founder deletion in Polish population.
Dymerska D, Gołębiewska K, Kuświk M, Rudnicka H, Scott RJ, Billings R, Pławski A, Boruń P, Siołek M, Kozak-Klonowska B, Szwiec M, Kilar E, Huzarski T, Byrski T, Lubinski J, Kurzawski G
J Clin Genet, 2017, 92 (6): 649-653, IF-3.326, MNiSW-30
„Nature” comments on the paper of Prof. M. Witt
In the latest issue of weekly Nature (2 Nov. 2017, vol. 551, p. 5), the Editorial was published commenting on the upcoming paper of Prof. Michał Witt, to be published in The American Journal of Medicine.