Mechanical isolation of the inner cell mass is effective in derivation of new human embryonic stem cell lines
Ström, Susanne, Inzunza, José, Grinnemo, Karl-Henrik, Holmberg, Kerstin, Matilainen, Eija, Strömberg, Anne-Marie, Blennow, Elisabeth, Hovatta, Outi
Published in Human reproduction (Oxford) (01.12.2007)
Published in Human reproduction (Oxford) (01.12.2007)
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In vitro culture conditions favoring selection of chromosomal abnormalities in human ES cells
Imreh, M.P., Gertow, K., Cedervall, J., Unger, C., Holmberg, K., Szöke, K., Csöregh, L., Fried, G., Dilber, S., Blennow, E., Ährlund-Richter, L.
Published in Journal of cellular biochemistry (01.10.2006)
Published in Journal of cellular biochemistry (01.10.2006)
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One-cell biopsy significantly improves the outcome of preimplantation genetic diagnosis (PGD) treatment: retrospective analysis of 569 PGD cycles at the Stockholm PGD centre
Haapaniemi Kouru, K., Malmgren, H., Nordenskjöld, M., Fridström, M., Csemiczky, G., Blennow, E.
Published in Human reproduction (Oxford) (01.09.2012)
Published in Human reproduction (Oxford) (01.09.2012)
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The frequency and prognostic impact of dic(9;20)(p13.2;q11.2) in childhood B-cell precursor acute lymphoblastic leukemia: results from the NOPHO ALL-2000 trial
ZACHARIADIS, V, GAUFFIN, F, CAVELIER, L, PALMQVIST, L, LÖNNERHOLM, G, NORDENSKJÖLD, M, JOHANSSON, B, FORESTIER, E, NORDGREN, A, KUCHINSKAYA, E, HEYMAN, M, SCHOUMANS, J, BLENNOW, E, GUSTAFSSON, B, BARBANY, G, GOLOVLEVA, I, EHRENCRONA, H
Published in Leukemia (01.04.2011)
Published in Leukemia (01.04.2011)
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Detailed molecular and clinical characterization of three patients with 21q deletions
Lindstrand, A, Malmgren, H, Sahlén, S, Schoumans, J, Nordgren, A, Ergander, U, Holm, E, Anderlid, BM, Blennow, E
Published in Clinical genetics (01.02.2010)
Published in Clinical genetics (01.02.2010)
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Preimplantation genetic diagnosis: twenty years of practice
Iwarsson, E, Malmgren, H, Blennow, E
Published in Seminars in fetal & neonatal medicine (01.04.2011)
Published in Seminars in fetal & neonatal medicine (01.04.2011)
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Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long‐term cultivation
Inzunza, J., Sahlén, S., Holmberg, K., Strömberg, A.‐M., Teerijoki, H., Blennow, E., Hovatta, O., Malmgren, H.
Published in Molecular human reproduction (01.06.2004)
Published in Molecular human reproduction (01.06.2004)
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Improved structural characterization of chromosomal breakpoints using high resolution custom array-CGH
Lindstrand, A, Schoumans, J, Gustavsson, P, Hanemaaijer, N, Malmgren, H, Blennow, E
Published in Clinical genetics (01.06.2010)
Published in Clinical genetics (01.06.2010)
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Frequent amplification of the Telomerase reverse transcriptase gene in human tumors
ANJU ZHANG, CHENGYUN ZHENG, NORDENSKJÖLD, Magnus, ZETTERBERG, Anders, BJÖRKHOLM, Magnus, GRUBER, Astrid, DAWEI XU, LINDVALL, Charlotta, MI HOU, EKEDAHL, Jessica, LEWENSOHN, Rolf, ZHONGQUN YAN, XIAOYAN YANG, HENRIKSSON, Marie, BLENNOW, Elisabeth
Published in Cancer research (Chicago, Ill.) (15.11.2000)
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Published in Cancer research (Chicago, Ill.) (15.11.2000)
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Tiling-resolution array-CGH reveals the pattern of DNA copy number alterations in acute lymphoblastic leukemia with 21q amplification: the result of telomere dysfunction and breakage fusion breakage cycles?
KUCHINSKAYA, E, NORDGREN, A, BLENNOW, E, HEYMAN, M, SCHOUMANS, J, CORCORAN, M, STAAF, J, BORG, A, SÖDERHALL, S, GRANDER, D, NORDENSKJÖLD, N
Published in Leukemia (01.06.2007)
Published in Leukemia (01.06.2007)
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Molecular cytogenetic characterization of a constitutional, highly complex intrachromosomal rearrangement of chromosome 1, with 14 breakpoints and a 0.5 Mb submicroscopic deletion
Lindstrand, A., Malmgren, H., Sahlén, S., Xin, H., Schoumans, J., Blennow, E.
Published in American journal of medical genetics. Part A (15.12.2008)
Published in American journal of medical genetics. Part A (15.12.2008)
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Limitations of Chromosome Classification by Multicolor Karyotyping
Lee, Charles, Gisselsson, David, Jin, Charlotte, Nordgren, Ann, Ferguson, David O., Blennow, Elisabeth, Fletcher, Jonathan A., Morton, Cynthia C.
Published in American journal of human genetics (01.04.2001)
Published in American journal of human genetics (01.04.2001)
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The position of t(11;22)(q23;q11) constitutional translocation breakpoint is conserved among its carriers
TAPIA-PAEZ, I, KOST-ALIMOVA, M, HU, P, ROE, B. A, BLENNOW, E, FEDOROVA, L, IMREH, S, DUMANSKI, J. P
Published in Human genetics (01.08.2001)
Published in Human genetics (01.08.2001)
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The performance of CGH array for the detection of cryptic constitutional chromosome imbalances
Schoumans, J, Anderlid, B-M, Blennow, E, Teh, B T, Nordenskjöld, M
Published in Journal of medical genetics (01.03.2004)
Published in Journal of medical genetics (01.03.2004)
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DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets
Mantripragada, Kiran Kumar, Tapia-Páez, Isabel, Blennow, Elisabeth, Nilsson, Peter, Wedell, Anna, Dumanski, Jan P
Published in International journal of molecular medicine (01.02.2004)
Published in International journal of molecular medicine (01.02.2004)
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Single cell CGH analysis reveals a high degree of mosaicism in human embryos from patients with balanced structural chromosome aberrations
Malmgren, H., Sahlén, S., Inzunza, J., Aho, M., Rosenlund, B., Fridström, M., Hovatta, O., Ährlund-Richter, L., Nordenskjöld, M., Blennow, E.
Published in Molecular human reproduction (01.05.2002)
Published in Molecular human reproduction (01.05.2002)
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Children and adults with acute lymphoblastic leukaemia have similar gene expression profiles
Kuchinskaya, E., Heyman, M., Grandér, D., Linderholm, M., Söderhäll, S., Zaritskey, A., Nordgren, A., Porwit-MacDonald, A., Zueva, E., Pawitan, Y., Corcoran, M., Nordenskjöld, M., Blennow, E.
Published in European journal of haematology (01.06.2005)
Published in European journal of haematology (01.06.2005)
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