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Page 1
Evolution of genetic techniques: past, present, and beyond.
Durmaz AA, Karaca E, Demkow U, Toruner G, Schoumans J, Cogulu O. Durmaz AA, et al. Among authors: schoumans j. Biomed Res Int. 2015;2015:461524. doi: 10.1155/2015/461524. Epub 2015 Mar 22. Biomed Res Int. 2015. PMID: 25874212 Free PMC article. Review.
Laboratory genetic testing in clinical practice 2014.
Cogulu O, Schoumans J, Toruner G, Demkow U, Karaca E, Durmaz AA. Cogulu O, et al. Among authors: schoumans j. Biomed Res Int. 2015;2015:574798. doi: 10.1155/2015/574798. Epub 2015 Mar 24. Biomed Res Int. 2015. PMID: 25879026 Free PMC article. No abstract available.
Laboratory Genetic Testing in Clinical Practice 2016.
Cogulu O, Schoumans J, Toruner G, Demkow U, Karaca E, Durmaz AA. Cogulu O, et al. Among authors: schoumans j. Biomed Res Int. 2017;2017:5798714. doi: 10.1155/2017/5798714. Epub 2017 Jan 4. Biomed Res Int. 2017. PMID: 28133609 Free PMC article. No abstract available.
Combined spectral karyotyping, comparative genomic hybridization, and in vitro apoptyping of a panel of Burkitt's lymphoma-derived B cell lines reveals an unexpected complexity of chromosomal aberrations and a recurrence of specific abnormalities in chemoresistant cell lines.
Karpova MB, Schoumans J, Blennow E, Ernberg I, Henter JI, Smirnov AF, Nordenskjöld M, Fadeel B. Karpova MB, et al. Among authors: schoumans j. Int J Oncol. 2006 Mar;28(3):605-17. Int J Oncol. 2006. PMID: 16465364
Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice.
Bruno DL, Ganesamoorthy D, Schoumans J, Bankier A, Coman D, Delatycki M, Gardner RJ, Hunter M, James PA, Kannu P, McGillivray G, Pachter N, Peters H, Rieubland C, Savarirayan R, Scheffer IE, Sheffield L, Tan T, White SM, Yeung A, Bowman Z, Ngo C, Choy KW, Cacheux V, Wong L, Amor DJ, Slater HR. Bruno DL, et al. Among authors: schoumans j. J Med Genet. 2009 Feb;46(2):123-31. doi: 10.1136/jmg.2008.062604. Epub 2008 Nov 17. J Med Genet. 2009. PMID: 19015223
t(15;21) translocations leading to the concurrent downregulation of RUNX1 and its transcription factor partner genes SIN3A and TCF12 in myeloid disorders.
L'Abbate A, Tolomeo D, De Astis F, Lonoce A, Lo Cunsolo C, Mühlematter D, Schoumans J, Vandenberghe P, Van Hoof A, Palumbo O, Carella M, Mazza T, Storlazzi CT. L'Abbate A, et al. Among authors: schoumans j. Mol Cancer. 2015 Dec 16;14:211. doi: 10.1186/s12943-015-0484-0. Mol Cancer. 2015. PMID: 26671595 Free PMC article.
The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language.
Anthoni H, Sucheston LE, Lewis BA, Tapia-Páez I, Fan X, Zucchelli M, Taipale M, Stein CM, Hokkanen ME, Castrén E, Pennington BF, Smith SD, Olson RK, Tomblin JB, Schulte-Körne G, Nöthen M, Schumacher J, Müller-Myhsok B, Hoffmann P, Gilger JW, Hynd GW, Nopola-Hemmi J, Leppanen PH, Lyytinen H, Schoumans J, Nordenskjöld M, Spencer J, Stanic D, Boon WC, Simpson E, Mäkelä S, Gustafsson JÅ, Peyrard-Janvid M, Iyengar S, Kere J. Anthoni H, et al. Among authors: schoumans j. Behav Genet. 2012 Jul;42(4):509-27. doi: 10.1007/s10519-012-9532-3. Epub 2012 Mar 17. Behav Genet. 2012. PMID: 22426781 Free PMC article.
94 results