Publications by authors named "Elisabeth Blennow"

43Publications

Clonal culturing of human embryonic stem cells on laminin-521/E-cadherin matrix in defined and xeno-free environment.

Nat Commun 2014 ;5:3195

1] Division of Matrix Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institute, Stockholm SE-171 77, Sweden [2] Cardiovascular and Metabolic Disorders Program, Duke-NUS, Singapore City 169857, Singapore.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/ncomms4195DOI Listing
October 2015

Inherited mosaicism for the supernumerary marker chromosome in cat eye syndrome: inter- and intra-individual variation and correlation to the phenotype.

Am J Med Genet A 2012 May 11;158A(5):1111-7. Epub 2012 Apr 11.

Clinical Genetics Unit, Department of Molecular Medicine and Surgery, Karolinska Institute, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ajmg.a.35311
Publisher Site
http://dx.doi.org/10.1002/ajmg.a.35311DOI Listing
May 2012

Hidden mosaicism for a structural chromosome rearrangement: a rare explanation for recurrent miscarriages and affected offspring?

Fertil Steril 2011 Feb 16;95(2):806-8. Epub 2010 Oct 16.

Department of Molecular Medicine and Surgery, Clinical Genetics Unit, Karolinska Institutet, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.fertnstert.2010.09.022DOI Listing
February 2011

Chimerism resulting from parthenogenetic activation and dispermic fertilization.

Am J Med Genet A 2010 Sep;152A(9):2277-86

Department of Molecular Medicine and Surgery and Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.33594DOI Listing
September 2010

Molecular and clinical characterization of patients with overlapping 10p deletions.

Am J Med Genet A 2010 May;152A(5):1233-43

Clinical Genetics Unit, Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.33366DOI Listing
May 2010

[More than 10 years with preimplantation genetic diagnosis in Sweden. An alternative when there is great risk of congenital diseases].

Lakartidningen 2008 Apr 2-8;105(14):1008-10

Klinisk genetik, Karolinska Universitetssjukhuset, Solna.

View Article

Download full-text PDF

Source
May 2008

Mechanical isolation of the inner cell mass is effective in derivation of new human embryonic stem cell lines.

Hum Reprod 2007 Dec 24;22(12):3051-8. Epub 2007 Oct 24.

Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/humrep/dem335DOI Listing
December 2007

Distal 3p deletion syndrome: detailed molecular cytogenetic and clinical characterization of three small distal deletions and review.

Am J Med Genet A 2007 Sep;143A(18):2143-9

Department of Molecular Medicine and Surgery, Clinical Genetics Unit, Karolinska Institutet, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.31902DOI Listing
September 2007

PGD for dystrophin gene deletions using fluorescence in situ hybridization.

Mol Hum Reprod 2006 May 11;12(5):353-6. Epub 2006 Apr 11.

Department of Molecular Medicine and Surgery, Clinical Genetics Unit, Karolinska Institutet and Fertility Unit, Karolinska University Hospital, Huddinge, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/molehr/gal039DOI Listing
May 2006

Molecular cytogenetic characterization of an insertional translocation, ins(6;7)(p25;q33q34): deletion/duplication of 7q33-34 and clinical correlations.

Am J Med Genet A 2005 Nov;139(1):25-31

Department of Molecular Medicine, Clinical Genetics Unit, Karolinska Institutet, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.30983DOI Listing
November 2005

Derivation of human embryonic stem cell lines in serum replacement medium using postnatal human fibroblasts as feeder cells.

Stem Cells 2005 Apr;23(4):544-9

Department of Clinical Sciences, Division of Obstetrics and Gynecology, Karolinska Institutet, Karolinska University Hospital, Huddinge, S-141 86 Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1634/stemcells.2004-0201
Publisher Site
http://dx.doi.org/10.1634/stemcells.2004-0201DOI Listing
April 2005

Combined genetic and transcriptional profiling of acute myeloid leukemia with normal and complex karyotypes.

Haematologica 2004 Sep;89(9):1072-81

Department of Molecular Medicine, Karolinska Hospital and Institutet, Stockholm, Sweden.

View Article

Download full-text PDF

Source
September 2004

A comparison of different metaphase CGH methods for the detection of cryptic chromosome aberrations of defined size.

Eur J Hum Genet 2004 Jun;12(6):447-54

Department of Molecular Medicine, Clinical Genetics Unit, Karolinska Institute, CMM L8:02, Stockholm SE-17176, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/sj.ejhg.5201175DOI Listing
June 2004

Reverse painting highlights the origin of chromosome aberrations.

Chromosome Res 2004 ;12(1):25-33

Department of Clinical Genetics, Karolinska Hospital, SE-171 76 Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1023/b:chro.0000009277.42798.9aDOI Listing
September 2004

DNA copy-number analysis of the 22q11 deletion-syndrome region using array-CGH with genomic and PCR-based targets.

Int J Mol Med 2004 Feb;13(2):273-9

Department of Genetics and Pathology, Rudbeck Laboratory, Uppsala University Hospital, SE-751 85 Uppsala, Sweden.

View Article

Download full-text PDF

Source
February 2004

A culture system using human foreskin fibroblasts as feeder cells allows production of human embryonic stem cells.

Hum Reprod 2003 Jul;18(7):1404-9

Department of Clinical Science, Karolinska Institutet, Huddinge University Hospital, S-141 86 Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/humrep/deg290DOI Listing
July 2003

Cryptic subtelomeric 6p deletion in a girl with congenital malformations and severe language impairment.

Eur J Hum Genet 2003 Jan;11(1):89-92

Department of Molecular Medicine, Clinical Genetics Unit, Karolinska Institutet at Karolinska Hospital, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1038/sj.ejhg.5200907DOI Listing
January 2003

Prenatal diagnosis: molecular genetics and cytogenetics.

Best Pract Res Clin Obstet Gynaecol 2002 Oct;16(5):629-43

Department of Molecular Medicine, Clinical Genetics Unit, Karolinska Institute, Karolinska Hospital, Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1053/beog.2002.0327DOI Listing
October 2002

[New analytic methods provide answers regarding chromosome aberrations in 1-2 days].

Lakartidningen 2002 Sep;99(37):3601-2

Centrum för fostermedicin, kvinnokliniken, Huddinge Universitetssjukhus.

View Article

Download full-text PDF

Source
September 2002

FISH-mapping of a 100-kb terminal 22q13 deletion.

Hum Genet 2002 May 4;110(5):439-43. Epub 2002 Apr 4.

Department of Molecular Medicine, CMM, L8:02, Clinical Genetics Unit, Karolinska Institutet at Karolinska Hospital, 171 76 Stockholm, Sweden.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-002-0713-7DOI Listing
May 2002

[Proposal for ethical guidelines concerning preimplantation genetic diagnosis].

Lakartidningen 2002 Mar;99(14):1568-73

Enheten för klinisk genetik, Sahlgrenska Universitetssjukhuset/Ostra, Göteborg.

View Article

Download full-text PDF

Source
March 2002

A region close to Tp53 shows LOH in familial breast cancer.

Int J Mol Med 2002 Apr;9(4):405-9

Department of Molecular Medicine, Karolinska Institute, 17176 Stockholm, Sweden.

View Article

Download full-text PDF

Source
April 2002