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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1993 1
1995 1
1996 2
1998 1
1999 1
2000 1
2001 3
2002 2
2003 5
2004 2
2005 2
2006 3
2007 2
2008 5
2009 3
2010 4
2011 4
2012 3
2013 5
2014 2
2015 3
2016 4
2017 1
2018 1
2019 5
2020 1
2021 2
2024 0

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64 results

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Page 1
The role of MAGT1 in genetic syndromes.
Trapani V, Shomer N, Rajcan-Separovic E. Trapani V, et al. Among authors: rajcan separovic e. Magnes Res. 2015 Jun;28(2):46-55. Magnes Res. 2015. PMID: 26422833 Free article. Review.
Chromosome microarrays in human reproduction.
Rajcan-Separovic E. Rajcan-Separovic E. Hum Reprod Update. 2012 Sep-Oct;18(5):555-67. doi: 10.1093/humupd/dms023. Epub 2012 Jun 2. Hum Reprod Update. 2012. PMID: 22661549 Review.
Comparative genomic hybridization of Wilms' tumor.
Rassekh SR, Rajcan-Separovic E. Rassekh SR, et al. Among authors: rajcan separovic e. Methods Mol Biol. 2013;973:249-65. doi: 10.1007/978-1-62703-281-0_16. Methods Mol Biol. 2013. PMID: 23412795 Review.
A genome-wide DNA methylation signature for SETD1B-related syndrome.
Krzyzewska IM, Maas SM, Henneman P, Lip KVD, Venema A, Baranano K, Chassevent A, Aref-Eshghi E, van Essen AJ, Fukuda T, Ikeda H, Jacquemont M, Kim HG, Labalme A, Lewis SME, Lesca G, Madrigal I, Mahida S, Matsumoto N, Rabionet R, Rajcan-Separovic E, Qiao Y, Sadikovic B, Saitsu H, Sweetser DA, Alders M, Mannens MMAM. Krzyzewska IM, et al. Among authors: rajcan separovic e. Clin Epigenetics. 2019 Nov 4;11(1):156. doi: 10.1186/s13148-019-0749-3. Clin Epigenetics. 2019. PMID: 31685013 Free PMC article.
Genotype-phenotype analysis of 18q12.1-q12.2 copy number variation in autism.
Wang P, Carrion P, Qiao Y, Tyson C, Hrynchak M, Calli K, Lopez-Rangel E, Andrieux J, Delobel B, Duban-Bedu B, Thuresson AC, Annerén G, Liu X, Rajcan-Separovic E, Suzanne Lewis ME. Wang P, et al. Among authors: rajcan separovic e. Eur J Med Genet. 2013 Aug;56(8):420-5. doi: 10.1016/j.ejmg.2013.05.006. Epub 2013 May 29. Eur J Med Genet. 2013. PMID: 23727450 Review.
Genomic characteristics of miscarriage copy number variants.
Bagheri H, Mercier E, Qiao Y, Stephenson MD, Rajcan-Separovic E. Bagheri H, et al. Among authors: rajcan separovic e. Mol Hum Reprod. 2015 Aug;21(8):655-61. doi: 10.1093/molehr/gav030. Epub 2015 Jun 12. Mol Hum Reprod. 2015. PMID: 26071097 Free PMC article.
Genomic imbalances in the placenta are associated with poor fetal growth.
Del Gobbo GF, Yin Y, Choufani S, Butcher EA, Wei J, Rajcan-Separovic E, Bos H, von Dadelszen P, Weksberg R, Robinson WP, Yuen RKC. Del Gobbo GF, et al. Among authors: rajcan separovic e. Mol Med. 2021 Jan 7;27(1):3. doi: 10.1186/s10020-020-00253-4. Mol Med. 2021. PMID: 33413077 Free PMC article.
Autism-associated familial microdeletion of Xp11.22.
Qiao Y, Liu X, Harvard C, Hildebrand MJ, Rajcan-Separovic E, Holden JJ, Lewis ME. Qiao Y, et al. Among authors: rajcan separovic e. Clin Genet. 2008 Aug;74(2):134-44. doi: 10.1111/j.1399-0004.2008.01028.x. Epub 2008 May 21. Clin Genet. 2008. PMID: 18498374
Whole exome sequencing in recurrent early pregnancy loss.
Qiao Y, Wen J, Tang F, Martell S, Shomer N, Leung PC, Stephenson MD, Rajcan-Separovic E. Qiao Y, et al. Among authors: rajcan separovic e. Mol Hum Reprod. 2016 May;22(5):364-72. doi: 10.1093/molehr/gaw008. Epub 2016 Jan 28. Mol Hum Reprod. 2016. PMID: 26826164 Free PMC article.
64 results