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Application of custom-designed oligonucleotide array CGH in 145 patients with autistic spectrum disorders.
Wiśniowiecka-Kowalnik B, Kastory-Bronowska M, Bartnik M, Derwińska K, Dymczak-Domini W, Szumbarska D, Ziemka E, Szczałuba K, Sykulski M, Gambin T, Gambin A, Shaw CA, Mazurczak T, Obersztyn E, Bocian E, Stankiewicz P. Wiśniowiecka-Kowalnik B, et al. Among authors: gambin t, gambin a. Eur J Hum Genet. 2013 Jun;21(6):620-5. doi: 10.1038/ejhg.2012.219. Epub 2012 Oct 3. Eur J Hum Genet. 2013. PMID: 23032108 Free PMC article.
National and subnational short-term forecasting of COVID-19 in Germany and Poland during early 2021.
Bracher J, Wolffram D, Deuschel J, Görgen K, Ketterer JL, Ullrich A, Abbott S, Barbarossa MV, Bertsimas D, Bhatia S, Bodych M, Bosse NI, Burgard JP, Castro L, Fairchild G, Fiedler J, Fuhrmann J, Funk S, Gambin A, Gogolewski K, Heyder S, Hotz T, Kheifetz Y, Kirsten H, Krueger T, Krymova E, Leithäuser N, Li ML, Meinke JH, Miasojedow B, Michaud IJ, Mohring J, Nouvellet P, Nowosielski JM, Ozanski T, Radwan M, Rakowski F, Scholz M, Soni S, Srivastava A, Gneiting T, Schienle M. Bracher J, et al. Among authors: gambin a. Commun Med (Lond). 2022 Oct 31;2(1):136. doi: 10.1038/s43856-022-00191-8. Commun Med (Lond). 2022. PMID: 36352249 Free PMC article.
Application of array comparative genomic hybridization in 102 patients with epilepsy and additional neurodevelopmental disorders.
Bartnik M, Szczepanik E, Derwińska K, Wiśniowiecka-Kowalnik B, Gambin T, Sykulski M, Ziemkiewicz K, Kędzior M, Gos M, Hoffman-Zacharska D, Mazurczak T, Jeziorek A, Antczak-Marach D, Rudzka-Dybała M, Mazurkiewicz H, Goszczańska-Ciuchta A, Zalewska-Miszkurka Z, Terczyńska I, Sobierajewicz M, Shaw CA, Gambin A, Mierzewska H, Mazurczak T, Obersztyn E, Bocian E, Stankiewicz P. Bartnik M, et al. Among authors: gambin t, gambin a. Am J Med Genet B Neuropsychiatr Genet. 2012 Oct;159B(7):760-71. doi: 10.1002/ajmg.b.32081. Epub 2012 Jul 23. Am J Med Genet B Neuropsychiatr Genet. 2012. PMID: 22825934
Inverted low-copy repeats and genome instability--a genome-wide analysis.
Dittwald P, Gambin T, Gonzaga-Jauregui C, Carvalho CM, Lupski JR, Stankiewicz P, Gambin A. Dittwald P, et al. Among authors: gambin t, gambin a. Hum Mutat. 2013 Jan;34(1):210-20. doi: 10.1002/humu.22217. Epub 2012 Oct 11. Hum Mutat. 2013. PMID: 22965494 Free PMC article.
Assessment of the role of copy-number variants in 150 patients with congenital heart defects.
Derwińska K, Bartnik M, Wiśniowiecka-Kowalnik B, Jagła M, Rudziński A, Pietrzyk JJ, Kawalec W, Ziółkowska L, Kutkowska-Kaźmierczak A, Gambin T, Sykulski M, Shaw CA, Gambin A, Mazurczak T, Obersztyn E, Bocian E, Stankiewicz P. Derwińska K, et al. Among authors: gambin t, gambin a. Med Wieku Rozwoj. 2012 Jul-Sep;16(3):175-82. Med Wieku Rozwoj. 2012. PMID: 23378395
NAHR-mediated copy-number variants in a clinical population: mechanistic insights into both genomic disorders and Mendelizing traits.
Dittwald P, Gambin T, Szafranski P, Li J, Amato S, Divon MY, Rodríguez Rojas LX, Elton LE, Scott DA, Schaaf CP, Torres-Martinez W, Stevens AK, Rosenfeld JA, Agadi S, Francis D, Kang SH, Breman A, Lalani SR, Bacino CA, Bi W, Milosavljevic A, Beaudet AL, Patel A, Shaw CA, Lupski JR, Gambin A, Cheung SW, Stankiewicz P. Dittwald P, et al. Among authors: gambin t, gambin a. Genome Res. 2013 Sep;23(9):1395-409. doi: 10.1101/gr.152454.112. Epub 2013 May 8. Genome Res. 2013. PMID: 23657883 Free PMC article.
Functional performance of aCGH design for clinical cytogenetics.
Gambin T, Stankiewicz P, Sykulski M, Gambin A. Gambin T, et al. Among authors: gambin a. Comput Biol Med. 2013 Jul;43(6):775-85. doi: 10.1016/j.compbiomed.2013.02.008. Epub 2013 Mar 16. Comput Biol Med. 2013. PMID: 23668354
87 results