Kristina Lagerstedt Robinson

Kristina Lagerstedt Robinson

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Kristina Lagerstedt Robinson

Kristina Lagerstedt Robinson

Publications by authors named "Kristina Lagerstedt Robinson"

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30Publications

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Genetic analyses supporting colorectal, gastric, and prostate cancer syndromes.

Genes Chromosomes Cancer 2019 11 7;58(11):775-782. Epub 2019 Aug 7.

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

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http://dx.doi.org/10.1002/gcc.22786DOI Listing
November 2019

Altered CSF levels of monoamines in hereditary spastic paraparesis 10: A case series.

Neurol Genet 2019 Aug 12;5(4):e344. Epub 2019 Jun 12.

Department of Neurology (M.A., K.S., G.S., M.P., P.S.), Karolinska University Hospital; Center for Neurology (M.A., P.S.), Academic Specialist Center; Department of Molecular Medicine and Surgery (K.L.-R.), Karolinska Institutet, and Department of Clinical Genetics, Karolinska University Hospital; Department of Clinical Neurophysiology (G.S.), Karolinska University Hospital, Stockholm; Department of Clinical Neuroscience (K.B.), University of Gothenburg; and Department of Clinical Neuroscience (M.A., K.S., G.S., M.P., P.S.), Karolinska Institutet, Stockholm, Sweden.

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http://dx.doi.org/10.1212/NXG.0000000000000344DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6659133PMC
August 2019

Parafibromin immunostainings of parathyroid tumors in clinical routine: a near-decade experience from a tertiary center.

Mod Pathol 2019 Jul 28;32(8):1082-1094. Epub 2019 Mar 28.

Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.

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http://dx.doi.org/10.1038/s41379-019-0252-6DOI Listing
July 2019

Benign paroxysmal torticollis of infancy does not lead to neurological sequelae.

Dev Med Child Neurol 2018 12 28;60(12):1251-1255. Epub 2018 Jun 28.

Department of Women's and Children's Health, Karolinska Institutet, Stockholm, Sweden.

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http://dx.doi.org/10.1111/dmcn.13939DOI Listing
December 2018

Testing strategies to reduce morbidity and mortality from Lynch syndrome.

Scand J Gastroenterol 2018 Dec 20;53(12):1535-1540. Epub 2018 Dec 20.

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

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http://dx.doi.org/10.1080/00365521.2018.1542453DOI Listing
December 2018

Chorea, psychosis, acanthocytosis, and prolonged survival associated with mutations.

Neurology 2018 10 14;91(15):710-712. Epub 2018 Sep 14.

From Karolinska University Hospital (M.P., A.P., C.F., M.D., J.L.-M., H.S., K.L., I.S., A. Wedell, A. Wredenberg, P.S.); Karolinska Institutet (M.P., A.P., C.F., Å.B., K.L., A. Wedell, A. Wredenberg, P.S.), Stockholm, Sweden; James J. Peters Veterans Medical Affair Center (R.H.W.), Bronx; and Mount Sinai School of Medicine (R.H.W.), New York, NY.

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http://www.neurology.org/lookup/doi/10.1212/WNL.000000000000
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http://dx.doi.org/10.1212/WNL.0000000000006320DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6177277PMC
October 2018

Genetic anticipation in Swedish Lynch syndrome families.

PLoS Genet 2017 Oct 31;13(10):e1007012. Epub 2017 Oct 31.

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

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http://dx.doi.org/10.1371/journal.pgen.1007012DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5681299PMC
October 2017

Mismatch repair gene mutation spectrum in the Swedish Lynch syndrome population.

Oncol Rep 2016 Nov 1;36(5):2823-2835. Epub 2016 Sep 1.

Department of Clinical Sciences, Division of Oncology and Pathology, Lund University, SE-22381 Lund, Sweden.

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http://dx.doi.org/10.3892/or.2016.5060DOI Listing
November 2016

Pathogenenic variant in the COL2A1 gene is associated with Spondyloepiphyseal dysplasia type Stanescu.

Am J Med Genet A 2016 Jan 30;170A(1):266-9. Epub 2015 Sep 30.

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

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http://dx.doi.org/10.1002/ajmg.a.37387DOI Listing
January 2016

GSTM1 gene expression correlates to leiomyoma volume regression in response to mifepristone treatment.

PLoS One 2013 4;8(12):e80114. Epub 2013 Dec 4.

Department of Women's and Children's Health, Division of Obstetrics and Gynecology, Karolinska Instituet, Karolinska University Hospital, Stockholm, Sweden.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0080114PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3851176PMC
September 2014

A case with bladder exstrophy and unbalanced X chromosome rearrangement.

Eur J Pediatr Surg 2014 Aug 25;24(4):353-9. Epub 2013 Jun 25.

Department of Women's and Children's Health, Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden.

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https://www.thieme-connect.com/products/ejournals/pdf/10.105
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http://www.thieme-connect.de/DOI/DOI?10.1055/s-0033-1349056
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http://dx.doi.org/10.1055/s-0033-1349056DOI Listing
August 2014

Partial tetrasomy 14 associated with multiple malformations.

Am J Med Genet A 2013 Jun 23;161A(6):1284-90. Epub 2013 Apr 23.

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

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http://dx.doi.org/10.1002/ajmg.a.35887DOI Listing
June 2013

Multigeneration Inheritance through Fertile XX Carriers of an NR0B1 (DAX1) Locus Duplication in a Kindred of Females with Isolated XY Gonadal Dysgenesis.

Int J Endocrinol 2012 28;2012:504904. Epub 2012 Feb 28.

Department of Molecular Medicine and Surgery, Karolinska Institut, Karolinska University Hospital, CMM L8:02, 17176 Stockholm, Sweden.

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http://dx.doi.org/10.1155/2012/504904DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3299259PMC
August 2012

Incidence of severe congenital neutropenia in Sweden and risk of evolution to myelodysplastic syndrome/leukaemia.

Br J Haematol 2012 Aug 25;158(3):363-9. Epub 2012 May 25.

Childhood Cancer Research Unit, Department of Women's and Children's Health, Karolinska Institutet, Karolinska University Hospital Solna, Stockholm, Sweden.

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http://dx.doi.org/10.1111/j.1365-2141.2012.09171.xDOI Listing
August 2012

Mutational study of the MAMLD1-gene in hypospadias.

Eur J Med Genet 2010 May-Jun;53(3):122-6. Epub 2010 Mar 25.

Department of Urology, The Second Hospital, Shandong University, Jinan 250033, PR China.

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http://linkinghub.elsevier.com/retrieve/pii/S176972121000021
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http://dx.doi.org/10.1016/j.ejmg.2010.03.005DOI Listing
October 2010

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.

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

No association between a promoter NOS1 polymorphism (rs41279104) and Infantile Hypertrophic Pyloric Stenosis.

J Hum Genet 2009 Dec 23;54(12):706-8. Epub 2009 Oct 23.

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

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http://dx.doi.org/10.1038/jhg.2009.101DOI Listing
December 2009