M. Soller

发表

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Yurii B. Shvetsov, Simon G. Coetzee, A. Whittemore, 2015, Nature Genetics.

Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer.

I. Panagopoulos, M. Isaksson, M. Soller, 2006, Genes, chromosomes & cancer.

Cytogenetic findings and clinical course in a consecutive series of Wilms tumors.

F. Mertens, T. Wiebe, M. Soller, 2003, Cancer genetics and cytogenetics.

The expression of pluripotency marker Oct 3/4 in prostate cancer and benign prostate hyperplasia

I. Panagopoulos, M. Isaksson, M. Soller, 2009, The Prostate.

dup(19)(q12q13.2): Array‐based Genotype–Phenotype Correlation of a New Possibly Obesity‐related Syndrome

J. Davidsson, M. Forsgren, A. Collin, 2010, Obesity.

Discrepancies between estimated and perceived risk of cancer among individuals with hereditary nonpolyposis colorectal cancer.

M. Nilbert, M. Soller, C. Carlsson, 2007, Genetic testing.

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

K. Ormond, Y. Bombard, B. Peterlin, 2015, European Journal of Human Genetics.

HIF1α isoforms in benign and malignant prostate tissue and their correlation to neuroendocrine differentiation

I. Panagopoulos, M. Soller, P. Abrahamsson, 2010, BMC Cancer.

HIF 1 alpha isoforms in benign and malignant prostate tissue and their correlation to neuroendocrine differentiation

I. Panagopoulos, M. Soller, P. Abrahamsson, 2010 .

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

Wei Lu, Wei Zheng, Mads Thomassen, 2013, Nature Genetics.

CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome

J. Schoumans, B. Anderlid, B. Anderlid, 2008, Clinical genetics.

Mutation update for the PORCN gene

R. Hennekam, J. Celli, R. Śmigiel, 2011, Human mutation.

How to Handle Genetic Information: A Comparison of Attitudes among Patients and the General Population

K. Nordin, M. Soller, H. Ehrencrona, 2010, Public Health Genomics.

Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross‐sectional study with healthcare professionals

K. Ormond, M. Choolani, I. Vogel, 2021, Prenatal diagnosis.

Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy

M. Dictor, M. Jerkeman, A. Dahlén, 2006, BMC Cancer.

Cytogenetic findings in pediatric renal cell carcinoma.

F. Mertens, J. Alumets, M. Soller, 2007, Cancer genetics and cytogenetics.

Short communication Cytogenetic findings in pediatric renal cell carcinoma

F. Mertens, J. Alumets, M. Soller, 2007 .

The gynecological surveillance of women with Lynch syndrome in Sweden.

P. Georgii‐Hemming, A. Lindblom, M. Mints, 2015, Gynecologic oncology.

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

J. Stoler, C. Garel, C. Depienne, 2017, Human Genetics.

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

K. Ormond, Y. Bombard, B. Peterlin, 2015, European Journal of Human Genetics.

Assessing women’s preferences towards tests that may reveal uncertain results from prenatal genomic testing: Development of attributes for a discrete choice experiment, using a mixed-methods design

K. Ormond, I. Vogel, L. Hui, 2022, PloS one.

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2

Mads Thomassen, Stephen Fox, Dieter Niederacher, 2011, Breast Cancer Research.

Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay

J. Davidsson, A. Collin, M. Soller, 2008, BMC Medical Genetics.

No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome

T. de Ravel, K. Devriendt, H. Van Esch, 2015, Orphanet Journal of Rare Diseases.

Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer

I. Panagopoulos, M. Isaksson, M. Soller, 2006 .

Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype–phenotype correlation and a comprehensive review of previously published cases

J. Davidsson, A. Collin, M. Soller, 2008, Epilepsy Research.

Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke

Sofie Samuelsson, Arne Lindgren, Ulf Kristoffersson, 2020, Stroke.

Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations

R. Hennekam, L. Biesecker, J. Graham, 2010, Human mutation.

The fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangement

D. Gisselsson, M. Johansson, B. Baldetorp, 2016, Scientific Reports.

Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data.

Mattias Höglund, David Gisselsson, D. Gisselsson, 2004, Cancer genetics and cytogenetics.

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

Sandra L. Halverson, A. Whittemore, L. Kiemeney, 2016, Gynecologic oncology.

Common Variants at the 19p13.1 and ZNF365 Loci Are Associated with ER Subtypes of Breast Cancer and Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

W. Chung, V. Pankratz, F. Couch, 2012, Cancer Epidemiology, Biomarkers & Prevention.

The BRCA1 exon 13 duplication in the Swedish population

A. Lindblom, B. Kremeyer, S. Mazoyer, 2004, Familial Cancer.

Screening of congenital heart disease patients using multiplex ligation‐dependent probe amplification: Early diagnosis of syndromic patients

T. Werge, J. Schouten, N. Tommerup, 2012, American journal of medical genetics. Part A.

Benchmarks for cystic fibrosis carrier screening: a European consensus document.

Milan Macek, Bruno Dallapiccola, Pier Franco Pignatti, 2010, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU

J. Stoler, C. Garel, C. Depienne, 2017, Human Genetics.

L. Feuk, B. V. van Bon, R. Pfundt, 2021, Genetics in Medicine.

Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients

A. Nordgren, J. Eisfeldt, D. Nilsson, 2021, Genome Medicine.

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

K. Ormond, Y. Bombard, B. Peterlin, 2015, European Journal of Human Genetics.

Relation between smoking history and gene expression profiles in lung adenocarcinomas

Johan Staaf, Mats Jönsson, Maria Planck, 2012, BMC Medical Genomics.

A model for karyotypic evolution in testicular germ cell tumors

D. Gisselsson, M. Höglund, F. Mitelman, 2004, Genes, chromosomes & cancer.

Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model

V. Fellman, E. Eklund, J. Kallijärvi, 2017, Orphanet Journal of Rare Diseases.

Familial aggregation of stroke amongst young patients in Lund Stroke Register

M. Soller, A. Ilinca, U. Kristoffersson, 2016, European journal of neurology.

Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis.

C. Gellera, M. Duno, F. Taroni, 2014, Parkinsonism & related disorders.

Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?

P. Bauer, L. Schöls, D. van Westen, 2014, Parkinsonism & Related Disorders.

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.

K. Ormond, Y. Bombard, B. Peterlin, 2015, European journal of human genetics : EJHG.

A stroke gene panel for whole-exome sequencing

A. Lindgren, M. Soller, A. Ilinca, 2018, European Journal of Human Genetics.

False‐positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha‐satellite probe (D18Z1) to chromosome 2

A. Collin, M. Soller, P. Sladkevicius, 2009, Prenatal diagnosis.

Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study.

P. Svenningsson, O. Hansson, L. Forsgren, 2019, Parkinsonism & related disorders.

Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?

P. Bauer, L. Schöls, D. Westen, 2014, Parkinsonism & related disorders.

Human Mutation MUTATION UPDATE Mutation Update for the PORCN Gene

R. Hennekam, J. Celli, R. Śmigiel, 2011 .

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

Sandra L. Halverson, A. Whittemore, L. Kiemeney, 2016, Gynecologic oncology.

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

Yurii B. Shvetsov, Simon G. Coetzee, Dennis J. Hazelett, 2014, Nature Genetics.

A stroke gene panel for whole-exome sequencing

A. Lindgren, M. Soller, A. Ilinca, 2018, European Journal of Human Genetics.

Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay

J. Davidsson, A. Collin, M. Soller, 2008, BMC Medical Genetics.

Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: a novel entity?

P. Bauer, L. Schöls, D. Westen, 2014, Parkinsonism & Related Disorders.