Maria Johansson Soller

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2015
Mark Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
Dondorp, Wybo ; de Wert, Guido ; Bombard, Yvonne ; Bianchi, Diana W ; Bergmann, Carsten ; Borry, Pascal ; Chitty, Lyn S ; Fellmann, Florence ; Forzano, Francesca and Hall, Alison , et al. (2015) In European Journal of Human Genetics 23(11). p.1438-1450
- Contribution to journal › Article
Mark Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
Dondorp, Wybo ; de Wert, Guido ; Bombard, Yvonne ; Bianchi, Diana W ; Bergmann, Carsten ; Borry, Pascal ; Chitty, Lyn S ; Fellmann, Florence ; Forzano, Francesca and Hall, Alison , et al. (2015) In European Journal of Human Genetics
- Contribution to journal › Article
Mark Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Kuchenbaecker, Karoline B ; Ramus, Susan J ; Tyrer, Jonathan ; Lee, Andrew ; Shen, Howard C ; Beesley, Jonathan ; Lawrenson, Kate ; McGuffog, Lesley ; Healey, Sue and Lee, Janet M , et al. (2015) In Nature Genetics 47(2). p.71-164
- Contribution to journal › Article
Mark The gynecological surveillance of women with Lynch syndrome in Sweden.
Tzortzatos, Gerasimos ; Andersson, Emil ; Soller, Maria ^LU ; Askmalm, Marie Stenmark ; Zagoras, Theofanis ; Georgii-Hemming, Patrik ; Lindblom, Annika ; Tham, Emma and Mints, Miriam (2015) In Gynecologic Oncology 138(3). p.717-722
- Contribution to journal › Article
Mark No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.
Schlögel, Matthieu J ; Mendola, Antonella ; Fastré, Elodie ; Vasudevan, Pradeep ; Devriendt, Koen ; de Ravel, Thomy Jl ; Van Esch, Hilde ; Casteels, Ingele ; Arroyo Carrera, Ignacio and Cristofoli, Francesca , et al. (2015) In Orphanet Journal of Rare Diseases 10(1).
- Contribution to journal › Article
2014
Mark Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: A novel entity?
Wictorin, Klas ^LU ; Brådvik, Björn ^LU ; Nilsson, Karin ^LU ; Soller, Maria ^LU ; van Westen, Danielle ^LU ; Bynke, Gunnel ^LU ; Bauer, Peter ; Schöls, Ludger and Puschmann, Andreas ^LU (2014) In Parkinsonism & Related Disorders 20(7). p.748-754
- Contribution to journal › Article
Mark Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis.
YGLAND, EMIL ^LU ; Taroni, Franco ; Gellera, Cinzia ; Caldarazzo, Serena ; Duno, Morten ; Soller, Maria ^LU and Puschmann, Andreas ^LU (2014) In Parkinsonism & Related Disorders 20(8). p.919-923
- Contribution to journal › Article
2013
Mark Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Bojesen, Stig E. ; Pooley, Karen A. ; Johnatty, Sharon E. ; Beesley, Jonathan ; Michailidou, Kyriaki ; Tyrer, Jonathan P. ; Edwards, Stacey L. ; Pickett, Hilda A. ; Shen, Howard C. and Smart, Chanel E. , et al. (2013) In Nature Genetics 45(4). p.371-384
- Contribution to journal › Article
2012
Mark Screening of Congenital Heart Disease Patients Using Multiplex Ligation-Dependent Probe Amplification: Early Diagnosis of Syndromic Patients
Sorensen, Karina Meden ; El-Segaier, Milad ^LU ; Fernlund, Eva ^LU ; Errami, Ab ; Bouvagnet, Patrice ; Nehme, Nancy ; Steensberg, Jesper ; Hjortdal, Vibeke ; Soller, Maria ^LU and Behjati, Mohaddeseh , et al. (2012) In American Journal of Medical Genetics. Part A 158A(4). p.720-725
- Contribution to journal › Article
Mark Relation between smoking history and gene expression profiles in lung adenocarcinomas
Staaf, Johan ^LU ; Jönsson, Göran B ^LU ; Jönsson, Mats ^LU ; Karlsson, Anna ; Isaksson, Sofi ^LU ; Salomonsson, Annette ^LU ; Pettersson, Helen ^LU ; Soller, Maria ^LU ; Ewers, Sven-Börje ^LU and Johansson, Leif ^LU , et al. (2012) In BMC Medical Genomics 5.
- Contribution to journal › Article