Lena Samuelsson

Lena Samuelsson

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Lena Samuelsson

Lena Samuelsson

Publications by authors named "Lena Samuelsson"

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24Publications

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Hyperestrogenism Affects Adult Height Outcome in Growth Hormone Treated Boys With Silver-Russell Syndrome.

Front Endocrinol (Lausanne) 2018 21;9:780. Epub 2018 Dec 21.

Department of Pediatrics, Göteborg Pediatric Growth Research Center, Institute of Clinical Sciences, The Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.

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http://dx.doi.org/10.3389/fendo.2018.00780DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6308318PMC
December 2018

On the significance of craniosynostosis in a case of Kabuki syndrome with a concomitant KMT2D mutation and 3.2 Mbp de novo 10q22.3q23.1 deletion.

Am J Med Genet A 2017 Aug 7;173(8):2219-2225. Epub 2017 Jun 7.

Department of Plastic Surgery, University of Gothenburg, The Sahlgrenska Academy, Gothenburg, Sweden.

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http://dx.doi.org/10.1002/ajmg.a.38296DOI Listing
August 2017

CTNND2-a candidate gene for reading problems and mild intellectual disability.

J Med Genet 2015 Feb 3;52(2):111-22. Epub 2014 Dec 3.

Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden Department of Clinical Genetics, Karolinska University Hospital, Stockholm, Sweden.

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http://dx.doi.org/10.1136/jmedgenet-2014-102757DOI Listing
February 2015

Inherited 15q24 microdeletion syndrome in twins and their father with phenotypic variability.

Eur J Med Genet 2015 Feb 16;58(2):111-5. Epub 2014 Dec 16.

Department of Pediatrics, Institute of Clinical Sciences, The Queen Silvia Children's Hospital, University of Gothenburg, Göteborg, Sweden; Department of Paediatrics, St. Olavs Hospital, Norway; Department of Laboratory Medicine, Children's and Women's Health, Norwegian University of Science and Technology, Trondheim, Norway. Electronic address:

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http://dx.doi.org/10.1016/j.ejmg.2014.12.006DOI Listing
February 2015

UBE2A deficiency syndrome: a report of two unrelated cases with large Xq24 deletions encompassing UBE2A gene.

Am J Med Genet A 2015 Jan 6;167A(1):204-10. Epub 2014 Oct 6.

Department of Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden.

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http://dx.doi.org/10.1002/ajmg.a.36800DOI Listing
January 2015

An emerging phenotype of Xq22 microdeletions in females with severe intellectual disability, hypotonia and behavioral abnormalities.

J Hum Genet 2014 Jun 20;59(6):300-6. Epub 2014 Mar 20.

1] Department of Clinical Genetics, Sahlgrenska University Hospital, Gothenburg, Sweden [2] Department of Medical and Clinical Genetics, Sahlgrenska Academy, Institute of Biomedicine, University of Gothenburg, Gothenburg, Sweden [3] Department of Clinical Genetics, University Hospital Linköping, Linköping, Sweden.

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http://dx.doi.org/10.1038/jhg.2014.21DOI Listing
June 2014

Surfactant protein A and albumin in particles in exhaled air.

Respir Med 2012 Feb 18;106(2):197-204. Epub 2011 Nov 18.

Occupational and Environmental Medicine, Sahlgrenska Academy, University of Gothenburg, Box 414, 405 30 Göteborg, Sweden.

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http://dx.doi.org/10.1016/j.rmed.2011.10.008DOI Listing
February 2012

Effects on airways of short-term exposure to two kinds of wood smoke in a chamber study of healthy humans.

Inhal Toxicol 2012 Jan;24(1):47-59

Department of Occupational and Environmental Medicine, Sahlgrenska University Hospital and Academy, University of Gothenburg, Gothenburg, Sweden.

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http://dx.doi.org/10.3109/08958378.2011.633281DOI Listing
January 2012

A genome-wide association study identifies new psoriasis susceptibility loci and an interaction between HLA-C and ERAP1.

Nat Genet 2010 Nov 17;42(11):985-90. Epub 2010 Oct 17.

Wellcome Trust Centre for Human Genetics, Oxford, UK.

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http://dx.doi.org/10.1038/ng.694DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3749730PMC
November 2010

Depression in Myotonic Dystrophy type 1: clinical and neuronal correlates.

Behav Brain Funct 2010 May 19;6:25. Epub 2010 May 19.

Neuromuscular Centre, Department of Neurology, Sahlgrenska University Hospital, Göteborg, Sweden.

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http://dx.doi.org/10.1186/1744-9081-6-25DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881877PMC
May 2010

Autism spectrum conditions in myotonic dystrophy type 1: a study on 57 individuals with congenital and childhood forms.

Am J Med Genet B Neuropsychiatr Genet 2008 Sep;147B(6):918-26

Department of Pediatrics, Northern Alvsborg County Hospital, Trollhättan, Sweden.

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http://doi.wiley.com/10.1002/ajmg.b.30698
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http://dx.doi.org/10.1002/ajmg.b.30698DOI Listing
September 2008

Analysis of chromosome 5q31-32 and psoriasis: confirmation of a susceptibility locus but no association with SNPs within SLC22A4 and SLC22A5.

J Invest Dermatol 2006 May;126(5):998-1002

Department of Clinical Genetics, Sahlgrenska University Hospital/Ostra, Smörslottsgatan 1, Göteborg University, Göteborg SE-41685, Sweden.

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http://dx.doi.org/10.1038/sj.jid.5700194DOI Listing
May 2006

Stress and well-being among parents of children with rare diseases: a prospective intervention study.

J Adv Nurs 2006 Feb;53(4):392-402

Assistant Professor, Department of Public Health and Community Medicine, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden.

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http://dx.doi.org/10.1111/j.1365-2648.2006.03736.xDOI Listing
February 2006

Analysis of 6 genetic loci for disease susceptibility in psoriatic arthritis.

J Rheumatol 2004 Nov;31(11):2230-5

Department of Public Health and Clinical Medicine, Rheumatology, University Hospital, Umeå, Sweden.

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November 2004

Multiplex ligation-dependent probe amplification (MLPA) detects large deletions in the MECP2 gene of Swedish Rett syndrome patients.

Genet Test 2003 ;7(4):329-32

Department of Clinical Genetics, Göteborg University, Sahlgrenska University Hospital/East, Göteborg, Sweden.

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http://dx.doi.org/10.1089/109065703322783707DOI Listing
October 2004

Association analysis of cystatin A and zinc finger protein 148, two genes located at the psoriasis susceptibility locus PSORS5.

J Invest Dermatol 2004 Jun;122(6):1399-400

Department of Clinical Genetics, Gothenburg University, East Hospital, Gothenburg, Sweden.

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http://dx.doi.org/10.1046/j.0022-202X.2004.12604.xDOI Listing
June 2004