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1.
Mapping of breakpoints in balanced chromosomal translocations by shallow whole-genome sequencing points to EFNA5, BAHD1 and PPP2R5E as novel candidates for genes causing human Mendelian disorders.
J Med Genet
; 56(2): 104-112, 2019 02.
Article
in English
| MEDLINE | ID: mdl-30352868
2.
Novel variants identified with next-generation sequencing in Polish patients with cone-rod dystrophy.
Mol Vis
; 24: 326-339, 2018.
Article
in English
| MEDLINE | ID: mdl-29769798
3.
Spaced seeds improve k-mer-based metagenomic classification.
Bioinformatics
; 31(22): 3584-92, 2015 Nov 15.
Article
in English
| MEDLINE | ID: mdl-26209798
4.
Gut Microbiome-How Does Two-Month Consumption of Fiber-Enriched Rolls Change Microbiome in Patients Suffering from MASLD?
Nutrients
; 16(8)2024 Apr 15.
Article
in English
| MEDLINE | ID: mdl-38674864
5.
Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders.
Am J Med Genet B Neuropsychiatr Genet
; 159B(7): 760-71, 2012 Oct.
Article
in English
| MEDLINE | ID: mdl-22825934
6.
Detection of clinically relevant exonic copy-number changes by array CGH.
Hum Mutat
; 31(12): 1326-42, 2010 Dec.
Article
in English
| MEDLINE | ID: mdl-20848651
7.
Truncated Robust Principal Component Analysis and Noise Reduction for Single Cell RNA Sequencing Data.
J Comput Biol
; 26(8): 782-793, 2019 08.
Article
in English
| MEDLINE | ID: mdl-31045436
8.
DNA enrichment and tagmentation method for species-level identification and strain-level differentiation using ON-rep-seq.
Commun Biol
; 2: 369, 2019.
Article
in English
| MEDLINE | ID: mdl-31633060
9.
Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15.
Eur J Med Genet
; 61(10): 596-601, 2018 Oct.
Article
in English
| MEDLINE | ID: mdl-29621621
10.
The association between 38 previously reported polymorphisms and psoriasis in a Polish population: High predicative accuracy of a genetic risk score combining 16 loci.
PLoS One
; 12(6): e0179348, 2017.
Article
in English
| MEDLINE | ID: mdl-28617847
11.
Gene Expression Profile of the Clinically Aggressive Micropapillary Variant of Bladder Cancer.
Eur Urol
; 70(4): 611-620, 2016 10.
Article
in English
| MEDLINE | ID: mdl-26988609
12.
Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability.
J Appl Genet
; 55(1): 125-44, 2014 Feb.
Article
in English
| MEDLINE | ID: mdl-24297458
13.
Functional performance of aCGH design for clinical cytogenetics.
Comput Biol Med
; 43(6): 775-85, 2013 Jul.
Article
in English
| MEDLINE | ID: mdl-23668354
14.
Multiple samples aCGH analysis for rare CNVs detection.
J Clin Bioinforma
; 3(1): 12, 2013 Jun 11.
Article
in English
| MEDLINE | ID: mdl-23758813
15.
Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders.
Eur J Hum Genet
; 21(6): 620-5, 2013 Jun.
Article
in English
| MEDLINE | ID: mdl-23032108
16.
Assessment of the role of copy-number variants in 150 patients with congenital heart defects.
Med Wieku Rozwoj
; 16(3): 175-82, 2012.
Article
in English
| MEDLINE | ID: mdl-23378395
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