Maria Johansson Soller

Publikationer
CV
Populärvetenskap och samverkan

Artiklar

Article: ACTA ANAESTHESIOLOGICA SCANDINAVICA. 2024;68(6):788-793
Malignant hyperthermia safety - A nationwide survey of publicly funded Swedish healthcare
Hellblom A; Miller WP; Soller M; Samuelsson C
Article: EUROPEAN JOURNAL OF MEDICAL GENETICS. 2023;66(8):104805
Lack of guidelines and translational knowledge is hindering the implementation of psychiatric genetic counseling and testing within Europe-A multi-professional survey study
Koido K; Malmgren CI; Pojskic L; Almos PZ; Bergen SE; Borg I; Bozina N; Coviello DA; Degenhardt F; Ganoci L; Jensen UB; Durand-Lennad L; Laurent-Levinson C; McQuillin A; Navickas A; Pace NP; Paneque M; Rietschel M; Grigoroiu-Serbanescu M; Soller MJ; Suvisaari J; Utkus A; Van Assche E; Vissouze L; Zuckerman S; Chaumette B; Tammimies K
Article: SCIENTIFIC REPORTS. 2023;13(1):6904
The cost-effectiveness of whole genome sequencing in neurodevelopmental disorders
Runheim H; Pettersson M; Hammarsjo A; Nordgren A; Henriksson M; Lindstrand A; Levin L-A; Soller MJ
Article: GENETICS IN MEDICINE. 2022;24(11):2296-2307
Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability
Lindstrand A; Ek M; Kvarnung M; Anderlid B-M; Bjoerck E; Carlsten J; Eisfeldt J; Grigelioniene G; Gustavsson P; Hammarsjoe A; Helgadottir HT; Hellstroem-Pigg M; Kuchinskaya E; Lagerstedt-Robinson K; Levin L-A; Lieden A; Lindeloef H; Malmgren H; Nilsson D; Svensson E; Paucar M; Sahlin E; Tesi B; Tham E; Winberg J; Winerdal M; Wincent J; Soller MJ; Pettersson M; Nordgren A
Article: PRENATAL DIAGNOSIS. 2022;42(7):934-946
Factor's that impact on women's decision-making around prenatal genomic tests: An international discrete choice survey
Buchanan J; Hill M; Vass CM; Hammond J; Riedijk S; Klapwijk JE; Harding E; Lou S; Vogel I; Hui L; Ingvoldstad-Malmgren C; Soller MJ; Ormond KE; Choolani M; Zheng Q; Chitty LS; Lewis C
Article: PLOS ONE. 2022;17(1):e0261898
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
Hammond J; Klapwijk JE; Riedijk S; Lou S; Ormond KE; Vogel I; Hui L; Sziepe E-J; Buchanan J; Ingvoldstad-Malmgren C; Soller MJ; Harding E; Hill M; Lewis C
Article: PLOS ONE. 2022;17(2):e0264056
A retrospective two centre study of Birt-Hogg-Dube syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population
Lagerstedt-Robinson K; Korberg IB; Tsiaprazis S; Bjorck E; Tham E; Poluha A; Pigg MH; Paulsson-Karlsson Y; Nordenskjold M; Johansson-Soller M; Aravidis C
Article: LAKARTIDNINGEN. 2021;118:21015
[The utility of whole genome sequencing in rare disease diagnostics].
Johansson Soller M; Nordgren A; Ehrencrona H; Lovmar L; Wedell A; Lindstrand A
Article: GENETICS IN MEDICINE. 2021;23(5):888-899
DLG4-related synaptopathy: a new rare brain disorder
Rodriguez-Palmero A; Boerrigter MM; Gomez-Andres D; Aldinger KA; Marcos-Alcalde I; Popp B; Everman DB; Lovgren AK; Arpin S; Bahrambeigi V; Beunders G; Bisgaard A-M; Bjerregaard VA; Bruel A-L; Challman TD; Cogne B; Coubes C; de Man SA; Denomme-Pichon A-S; Dye TJ; Elmslie F; Feuk L; Garcia-Minaur S; Gertler T; Giorgio E; Gruchy N; Haack TB; Haldeman-Englert CR; Haukanes BI; Hoyer J; Hurst ACE; Isidor B; Soller MJ; Kushary S; Kvarnung M; Landau YE; Leppig KA; Lindstrand A; Kleinendorst L; MacKenzie A; Mandrile G; Mendelsohn BA; Moghadasi S; Morton JE; Moutton S; Mueller AJ; O'Leary M; Pacio-Miguez M; Palomares-Bralo M; Parikh S; Pfundt R; Pode-Shakked B; Rauch A; Repnikova E; Revah-Politi A; Ross MJ; Ruivenkamp CAL; Sarrazin E; Savatt JM; Schlueter A; Schoenewolf-Greulich B; Shad Z; Shaw-Smith C; Shieh JT; Shohat M; Spranger S; Thiese H; Mau-Them FT; van Bon B; van de Burgt I; van de Laar IMBH; van Drie E; van Haelst MM; van Ravenswaaij-Arts CM; Verdura E; Vitobello A; Waldmueller S; Whiting S; Zweier C; Prada CE; de Vries BBA; Dobyns WB; Reiter SF; Gomez-Puertas P; Pujol A; Tumer Z
Article: PRENATAL DIAGNOSIS. 2021;41(6):720-732
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals
Lewis C; Hammond J; Klapwijk JE; Harding E; Lou S; Vogel I; Szepe EJ; Hui L; Ingvoldstad-Malmgren C; Soller MJ; Ormond KE; Choolani M; Hill M; Riedijk S
Article: GENOME MEDICINE. 2021;13(1):40
Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients
Stranneheim H; Lagerstedt-Robinson K; Magnusson M; Kvarnung M; Nilsson D; Lesko N; Engvall M; Anderlid B-M; Arnell H; Johansson CB; Barbaro M; Bjorck E; Bruhn H; Eisfeldt J; Freyer C; Grigelioniene G; Gustavsson P; Hammarsjo A; Hellstrom-Pigg M; Iwarsson E; Jemt A; Laaksonen M; Enoksson SL; Malmgren H; Naess K; Nordenskjold M; Oscarson M; Pettersson M; Rasi C; Rosenbaum A; Sahlin E; Sardh E; Stodberg T; Tesi B; Tham E; Thonberg H; Tohonen V; von Dobeln U; Vassiliou D; Vonlanthen S; Wikstrom A-C; Wincent J; Winqvist O; Wredenberg A; Ygberg S; Zetterstrom RH; Marits P; Soller MJ; Nordgren A; Wirta V; Lindstrand A; Wedell A
Article: STROKE. 2020;51(4):1056-1063
Whole-Exome Sequencing in 22 Young Ischemic Stroke Patients With Familial Clustering of Stroke
Ilinca A; Martinez-Majander N; Samuelsson S; Piccinelli P; Truve K; Cole J; Kittner S; Soller M; Kristoffersson U; Tatlisumak T; Puschmann A; Putaala J; Lindgren A
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019;27(12):1763-1773
European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death
Fellmann F; van El CG; Charron P; Michaud K; Howard HC; Boers SN; Clarke AJ; Duguet A-M; Forzano F; Kauferstein S; Kayserili H; Lucassen A; Mendes A; Patch C; Radojkovic D; Rial-Sebbag E; Sheppard MN; Tasse A-M; Temel SG; Sajantila A; Basso C; Wilde AAM; Cornel MC; Benjamin C; Borry P; Clarke A; Cordier C; Cornel M; van El C; Fellmann F; Forzano F; Howard H; Kayserili H; Melegh B; Mendes A; Perola M; Peterlin B; Radojkovic D; Rial-Sebbag E; Rogowski W; Soller M; Stefansdottir V; de Wert G
Article: GENOME MEDICINE. 2019;11(1):68
From cytogenetics to cytogenomics: whole-genome sequencing as a first-line test comprehensively captures the diverse spectrum of disease-causing genetic variation underlying intellectual disability
Lindstrand A; Eisfeldt J; Pettersson M; Carvalho CMB; Kvarnung M; Grigelioniene G; Anderlid B-M; Bjerin O; Gustavsson P; Hammarsjo A; Georgii-Hemming P; Iwarsson E; Johansson-Soller M; Lagerstedt-Robinson K; Lieden A; Magnusson M; Martin M; Malmgren H; Nordenskjold M; Norling A; Sahlin E; Stranneheim H; Tham E; Wincent J; Ygberg S; Wedell A; Wirta V; Nordgren A; Lundin J; Nilsson D
Article: PARKINSONISM AND RELATED DISORDERS. 2019;66:158-165
Low prevalence of known pathogenic mutations in dominant PD genes: A Swedish multicenter study
Puschmann A; Jimenez-Ferrer I; Lundblad-Andersson E; Martensson E; Hansson O; Odin P; Widner H; Brolin K; Mzezewa R; Kristensen J; Soller M; Rodstrom EY; Ross OA; Toft M; Breedveld GJ; Bonifati V; Brodin L; Zettergren A; Sydow O; Linder J; Wirdefeldt K; Svenningsson P; Nissbrandt H; Belin AC; Forsgren L; Swanberg M
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2019;27(2):317-324
A stroke gene panel for whole-exome sequencing
Ilinca A; Samuelsson S; Piccinelli P; Soller M; Kristoffersson U; Lindgren AG
Article: ORPHANET JOURNAL OF RARE DISEASES. 2017;12(1):73
Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
Tegelberg S; Tomasic N; Kallijarvi J; Purhonen J; Elmer E; Lindberg E; Nord DG; Soller M; Lesko N; Wedell A; Bruhn H; Freyer C; Stranneheim H; Wibom R; Nennesmo I; Wredenberg A; Eklund EA; Fellman V
Article: HUMAN GENETICS. 2017;136(4):463-479
Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU
Depienne C; Nava C; Keren B; Heide S; Rastetter A; Passemard S; Chantot-Bastaraud S; Moutard M-L; Agrawal PB; VanNoy G; Stoler JM; Amor DJ; de Villemeur TB; Doummar D; Alby C; Cormier-Daire V; Garel C; Marzin P; Scheidecker S; de Saint-Martin A; Hirsch E; Korff C; Bottani A; Faivre L; Verloes A; Orzechowski C; Burglen L; Leheup B; Roume J; Andrieux J; Sheth F; Datar C; Parker MJ; Pasquier L; Odent S; Naudion S; Delrue M-A; Le Caignec C; Vincent M; Isidor B; Renaldo F; Stewart F; Toutain A; Koehler U; Hackl B; von Stulpnagel C; Kluger G; Moller RS; Pal D; Jonson T; Soller M; Verbeek NE; van Haelst MM; de Kovel C; Koeleman B; Monroe G; van Haaften G; Study DDD; Attie-Bitach T; Boutaud L; Heron D; Mignot C
Article: SCIENTIFIC REPORTS. 2016;6:23500
The fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangement
Valind A; Haika C; Klasson MEK; Johansson MC; Gullander J; Soller M; Baldetorp B; Gisselsson D
Article: EUROPEAN JOURNAL OF NEUROLOGY. 2016;23(2):401-407
Familial aggregation of stroke amongst young patients in Lund Stroke Register
Ilinca A; Kristoffersson U; Soller M; Lindgren AG
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015;23(11):1438-1450
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
Dondorp W; de Wert G; Bombard Y; Bianchi DW; Bergmann C; Borry P; Chitty LS; Fellmann F; Forzano F; Hall A; Henneman L; Howard HC; Lucassen A; Ormond K; Peterlin B; Radojkovic D; Rogowski W; Soller M; Tibben A; Tranebjaerg L; van El CG; Cornel MC
Article: GYNECOLOGIC ONCOLOGY. 2015;138(3):717-722
The gynecological surveillance of women with Lynch Syndrome in Sweden
Tzortzatos G; Andersson E; Soller M; Askmalm MS; Zagoras T; Georgii-Hemming P; Lindblom A; Tham E; Mints M
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015;23(6):729-735
Points to consider for prioritizing clinical genetic testing services: a European consensus process oriented at accountability for reasonableness
Severin F; Borry P; Cornel MC; Daniels N; Fellmann F; Hodgson SV; Howard HC; John J; Kaariainen H; Kayserili H; Kent A; Koerber F; Kristoffersson U; Kroese M; Lewis C; Marckmann G; Meyer P; Pfeufer A; Schmidtke J; Skirton H; Tranebjaerg L; Rogowski WH
Article: ORPHANET JOURNAL OF RARE DISEASES. 2015;10:52
No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome
Schlogel MJ; Mendola A; Fastre E; Vasudevan P; Devriendt K; de Ravel TJL; Van Esch H; Casteels I; Arroyo Carrera I; Cristofoli F; Fieggen K; Jones K; Lipson M; Balikova I; Singer A; Soller M; Mercedes Villanueva M; Revencu N; Boon LM; Brouillard P; Vikkula M
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations.
Dondorp W; de Wert G; Bombard Y; Bianchi DW; Bergmann C; Borry P; Chitty LS; Fellmann F; Forzano F; Hall A; Henneman L; Howard HC; Lucassen A; Ormond K; Peterlin B; Radojkovic D; Rogowski W; Soller M; Tibben A; Tranebjærg L; van El CG; Cornel MC
Article: NATURE GENETICS. 2015;47(2):164-171
Identification of six new susceptibility loci for invasive epithelial ovarian cancer
Kuchenbaecker KB; Ramus SJ; Tyrer J; Lee A; Shen HC; Beesley J; Lawrenson K; McGuffog L; Healey S; Lee JM; Spindler TJ; Lin YG; Pejovic T; Bean Y; Li Q; Coetzee S; Hazelett D; Miron A; Southey M; Terry MB; Goldgar DE; Buys SS; Janavicius R; Dorfling CM; van Rensburg EJ; Neuhausen SL; Ding YC; Hansen TVO; Jonson L; Gerdes A-M; Ejlertsen B; Barrowdale D; Dennis J; Benitez J; Osorio A; Garcia MJ; Komenaka I; Weitzel JN; Ganschow P; Peterlongo P; Bernard L; Viel A; Bonanni B; Peissel B; Manoukian S; Radice P; Papi L; Ottini L; Fostira F; Konstantopoulou I; Garber J; Frost D; Perkins J; Platte R; Ellis S; Godwin AK; Schmutzler RK; Meindl A; Engel C; Sutter C; Sinilnikova OM; Damiola F; Mazoyer S; Stoppa-Lyonnet D; Claes K; De Leeneer K; Kirk J; Rodriguez GC; Piedmonte M; O'Malley DM; de la Hoya M; Caldes T; Aittomaeki K; Nevanlinna H; Collee JM; Rookus MA; Oosterwijk JC; Tihomirova L; Tung N; Hamann U; Isaccs C; Tischkowitz M; Imyanitov EN; Caligo MA; Campbell IG; Hogervorst FBL; Olah E; Diez O; Blanco I; Brunet J; Lazaroso C; Angel Pujana M; Jakubowska A; Gronwald J; Lubinski J; Sukiennicki G; Barkardottir RB; Plante M; Simard J; Soucy P; Montagna M; Tognazzo S; Teixeira MR; Pankratz VS; Wang X; Lindor N; Szabo CI; Kauff N; Vijai J; Aghajanian CA; Pfeiler G; Berger A; Singer CF; Tea M-K; Phelan CM; Greene MH; Mai PL; Rennert G; Mulligan AM; Tchatchou S; Andrulis IL; Glendon G; Toland AE; Jensen UB; Kruse TA; Thomassen M; Bojesen A; Zidan J; Friedman E; Laitman Y; Soller M; Liljegren A; Arver B; Einbeigi Z; Stenmark-Askmalm M; Olopade OI; Nussbaum RL; Rebbeck TR; Nathanson KL; Domchek SM; Lu KH; Karlan BY; Walsh C; Lester J; Hein A; Ekici AB; Beckmann MW; Fasching PA; Lambrechts D; Van Nieuwenhuysen E; Vergote I; Lambrechts S; Dicks E; Doherty JA; Wicklund KG; Rossing MA; Rudolph A; Chang-Claude J; Wang-Gohrke S; Eilber U; Moysich KB; Odunsi K; Sucheston L; Lele S; Wilkens LR; Goodman MT; Thompson PJ; Shvetsov YB; Runnebaum IB; Duerst M; Hillemanns P; Doerk T; Antonenkova N; Bogdanova N; Leminen A; Pelttari LM; Butzow R; Modugno F; Kelley JL; Edwards RP; Ness RB; du Bois A; Heitz F; Schwaab I; Harter P; Matsuo K; Hosono S; Orsulic S; Jensen A; Kjaer SK; Hogdall E; Hasmad HN; Azmi MAN; Teo S-H; Woo Y-L; Fridley BL; Goode EL; Cunningham JM; Vierkant RA; Bruinsma F; Giles GG; Liang D; Hildebrandt MAT; Wu X; Levine DA; Bisogna M; Berchuck A; Iversen ES; Schildkraut JM; Concannon P; Weber RP; Cramer DW; Terry KL; Poole EM; Tworoger SS; Bandera EV; Orlow I; Olson SH; Krakstad C; Salvesen HB; Tangen IL; Bjorge L; van Altena AM; Aben KKH; Kiemeney LA; Massuger LFAG; Kellar M; Brooks-Wilson A; Kelemen LE; Cook LS; Le ND; Cybulski C; Yang H; Lissowska J; Brinton LA; Wentzensen N; Hogdall C; Lundvall L; Nedergaard L; Baker H; Song H; Eccles D; McNeish I; Paul J; Carty K; Siddiqui N; Glasspool R; Whittemore AS; Rothstein JH; McGuire V; Sieh W; Ji B-T; Zheng W; Shu X-O; Gao Y-T; Rosen B; Risch HA; McLaughlin JR; Narod SA; Monteiro AN; Chen A; Lin H-Y; Permuth-Wey J; Sellers TA; Tsai Y-Y; Chen Z; Ziogas A; Anton-Culver H; Gentry-Maharaj A; Menon U; Harrington P; Lee AW; Wu AH; Pearce CL; Coetzee G; Pike MC; Dansonka-Mieszkowska A; Timorek A; Rzepecka IK; Kupryjanczyk J; Freedman M; Noushmehr H; Easton DF; Offit K; Couch FJ; Gayther S; Pharoah PP; Antoniou AC; Chenevix-Trench G
Article: PLOS ONE. 2015;10(4):e0120020
Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers
Blanco I; Kuchenbaecker K; Cuadras D; Wang X; Barrowdale D; Ruiz de Garibay G; Librado P; Sanchez-Gracia A; Rozas J; Bonifaci N; McGuffog L; Pankratz VS; Islam A; Mateo F; Berenguer A; Petit A; Catala I; Brunet J; Feliubadalo L; Tornero E; Benitez J; Osorio A; Cajal TRY; Nevanlinna H; Aittomaki K; Arun BK; Toland AE; Karlan BY; Walsh C; Lester J; Greene MH; Mai PL; Nussbaum RL; Andrulis IL; Domchek SM; Nathanson KL; Rebbeck TR; Barkardottir RB; Jakubowska A; Lubinski J; Durda K; Jaworska-Bieniek K; Claes K; Van Maerken T; Diez O; Hansen TV; Jonson L; Gerdes A-M; Ejlertsen B; de la Hoya M; Caldes T; Dunning AM; Oliver C; Fineberg E; Cook M; Peock S; McCann E; Murray A; Jacobs C; Pichert G; Lalloo F; Chu C; Dorkins H; Paterson J; Ong K-R; Teixeira MR; Teixeira; Hogervorst FBL; van der Hout AH; Seynaeve C; van der Luijt RB; Ligtenberg MJL; Devilee P; Wijnen JT; Rookus MA; Meijers-Heijboer HEJ; Blok MJ; van den Ouweland AMW; Aalfs CM; Rodriguez GC; Phillips K-AA; Piedmonte M; Nerenstone SR; Bae-Jump VL; O'Malley DM; Ratner ES; Schmutzler RK; Wappenschmidt B; Rhiem K; Engel C; Meindl A; Ditsch N; Arnold N; Plendl HJ; Niederacher D; Sutter C; Wang-Gohrke S; Steinemann D; Preisler-Adams S; Kast K; Varon-Mateeva R; Gehrig A; Bojesen A; Pedersen IS; Sunde L; Jensen UB; Thomassen M; Kruse TA; Foretova L; Peterlongo P; Bernard L; Peissel B; Scuvera G; Manoukian S; Radice P; Ottini L; Montagna M; Agata S; Maugard C; Simard J; Soucy P; Berger A; Fink-Retter A; Singer CF; Rappaport C; Geschwantler-Kaulich D; Tea M-K; Pfeiler G; John EM; Miron A; Neuhausen SL; Terry MB; Chung WK; Daly MB; Goldgar DE; Janavicius R; Dorfling CM; van Rensburg EJ; Fostira F; Konstantopoulou I; Garber J; Godwin AK; Olah E; Narod SA; Rennert G; Paluch SS; Laitman Y; Friedman E; Liljegren A; Rantala J; Stenmark-Askmalm M; Loman N; Imyanitov EN; Hamann U; Spurdle AB; Healey S; Weitzel JN; Herzog J; Margileth D; Gorrini C; Esteller M; Gomez A; Sayols S; Vidal E; Heyn H; Stoppa-Lyonnet D; Leone M; Barjhoux L; Fassy-Colcombet M; de Pauw A; Lasset C; Ferrer SF; Castera L; Berthet P; Cornelis F; Bignon Y-J; Damiola F; Mazoyer S; Sinilnikova OM; Maxwell CA; Vijai J; Robson M; Kauff N; Corines MJ; Villano D; Cunningham J; Lee A; Lindor N; Lazaro C; Easton DF; Offit K; Chenevix-Trench G; Couch FJ; Antoniou AC; Angel Pujana M
Article: PARKINSONISM AND RELATED DISORDERS. 2014;20(8):919-923
Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis
Ygland E; Taroni F; Genera C; Caldarazzo S; Duno M; Soller M; Puschmann A
Article: PARKINSONISM AND RELATED DISORDERS. 2014;20(7):748-754
Autosomal dominant cerebellar ataxia with slow ocular saccades, neuropathy and orthostatism: A novel entity?
Wictorin K; Bradvik B; Nilsson K; Soller M; van Westen D; Bynke G; Bauer P; Schoels L; Puschmann A
Article: NATURE GENETICS. 2013;45(4):371-384
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
Bojesen SE; Pooley KA; Johnatty SE; Beesley J; Michailidou K; Tyrer JP; Edwards SL; Pickett HA; Shen HC; Smart CE; Hillman KM; Mai PL; Lawrenson K; Stutz MD; Lu Y; Karevan R; Woods N; Johnston RL; French JD; Chen X; Weischer M; Nielsen SF; Maranian MJ; Ghoussaini M; Ahmed S; Baynes C; Bolla MK; Wang Q; Dennis J; McGuffog L; Barrowdale D; Lee A; Healey S; Lush M; Tessier DC; Vincent D; Bacot F; Vergote I; Lambrechts S; Despierre E; Risch HA; Gonzalez-Neira A; Rossing MA; Pita G; Doherty JA; Alvarez N; Larson MC; Fridley BL; Schoof N; Chang-Claude J; Cicek MS; Peto J; Kalli KR; Broeks A; Armasu SM; Schmidt MK; Braaf LM; Winterhoff B; Nevanlinna H; Konecny GE; Lambrechts D; Rogmann L; Guenel P; Teoman A; Milne RL; Garcia JJ; Cox A; Shridhar V; Burwinkel B; Marme F; Hein R; Sawyer EJ; Haiman CA; Wang-Gohrke S; Andrulis IL; Moysich KB; Hopper JL; Odunsi K; Lindblom A; Giles GG; Brenner H; Simard J; Lurie G; Fasching PA; Carney ME; Radice P; Wilkens LR; Swerdlow A; Goodman MT; Brauch H; Garcia-Closas M; Hillemanns P; Winqvist R; Durst M; Devilee P; Runnebaum I; Jakubowska A; Lubinski J; Mannermaa A; Butzow R; Bogdanova NV; Doerk T; Pelttari LM; Zheng W; Leminen A; Anton-Culver H; Bunker CH; Kristensen V; Ness RB; Muir K; Edwards R; Meindl A; Heitz F; Matsuo K; du Bois A; Wu AH; Harter P; Teo S-H; Schwaab I; Shu X-O; Blot W; Hosono S; Kang D; Nakanishi T; Hartman M; Yatabe Y; Hamann U; Karlan BY; Sangrajrang S; Kjaer SK; Gaborieau V; Jensen A; Eccles D; Hogdall E; Shen C-Y; Brown J; Woo YL; Shah M; Azmi MAN; Luben R; Omar SZ; Czene K; Vierkant RA; Nordestgaard BG; Flyger H; Vachon C; Olson JE; Wang X; Levine DA; Rudolph A; Weber RP; Flesch-Janys D; Iversen E; Nickels S; Schildkraut JM; Silva IDS; Cramer DW; Gibson L; Terry KL; Fletcher O; Vitonis AF; van der Schoot CE; Poole EM; Hogervorst FBL; Tworoger SS; Liu J; Bandera EV; Li J; Olson SH; Humphreys K; Row I; Blomqvist C; Rodriguez-Rodriguez L; Aittomaki K; Salvesen HB; Muranen TA; Wik E; Brouwers B; Krakstad C; Wauters E; Halle MK; Wildiers H; Kiemeney LA; Mulot C; Aben KK; Laurent-Puig P; Altena AM; Therese T; Massuger LFAG; Benitez J; Pejovic T; Arias Perez JI; Hoatlin M; Zamora MP; Cook LS; Balasubramanian SP; Kelemen LE; Schneeweiss A; Le ND; Sohn C; Brooks-Wilson A; Tomlinson I; Kerin MJ; Miller N; Cybulski C; Henderson BE; Menkiszak J; Schumacher F; Wentzensen N; Marchand LL; Yang HP; Mulligan AM; Glendon G; Engelholm SA; Knight JA; Hogdall CK; Apicella C; Gore M; Tsimiklis H; Song H; Southey MC; Jager A; den Ouweland AMW; Brown R; Martens JWM; Flanagan JM; Kriege M; Paul J; Margolin S; Siddiqui N; Severi G; Whittemore AS; Baglietto L; McGuire V; Stegmaier C; Sieh W; Mueller H; Arndt V; Labreche F; Gao Y-T; Goldberg MS; Yang G; Dumont M; McLaughlin JR; Hartmann A; Ekici AB; Beckmann MW; Phelan CM; Lux MP; Permuth-Wey J; Peissel B; Sellers TA; Ficarazzi F; Barile M; Ziogas A; Ashworth A; Gentry-Maharaj A; Jones M; Ramus SJ; Orr N; Menon U; Pearce CL; Bruening T; Pike MC; Ko Y-D; Lissowska J; Figueroa J; Kupryjanczyk J; Chanock SJ; Dansonka-Mieszkowska A; Jukkola-Vuorinen A; Rzepecka IK; Pylkas K; Bidzinski M; Kauppila S; Hollestelle A; Seynaeve C; Tollenaar RAEM; Durda K; Jaworska K; Hartikainen JM; Kosma V-M; Kataja V; Antonenkova NN; Long J; Shrubsole M; Deming-Halverson S; Lophatananon A; Siriwanarangsan P; Stewart-Brown S; Ditsch N; Lichtner P; Schmutzler RK; Ito H; Iwata H; Tajima K; Tseng C-C; Stram DO; van den Berg D; Yip CH; Ikrarn MK; Teh Y-C; Cai H; Lu W; Signorello LB; Cai Q; Noh D-Y; Yoo K-Y; Miao H; Iau PT-C; Teo YY; McKay J; Shapiro C; Ademuyiwa F; Fountzilas G; Hsiung C-N; Yu J-C; Hou M-F; Healey CS; Luccarini C; Peock S; Stoppa-Lyonnet D; Peterlongo P; Rebbeck TR; Piedmonte M; Singer CF; Friedman E; Thomassen M; Offit K; Hansen TVO; Neuhausen SL; Szabo CI; Blanco I; Garber J; Narod SA; Weitzel JN; Montagna M; Olah E; Godwin AK; Yannoukakos D; Goldgar DE; Caldes T; Imyanitov EN; Tihomirova L; Arun BK; Campbell I; Mensenkamp AR; van Asperen CJ; van Roozendaa KEP; Meijers-Heijboer H; Collee JM; Oosterwijk JC; Hooning MJ; Rookus MA; van der Luijt RB; Os TAM; Evans DG; Frost D; Fineberg E; Barwell J; Walker L; Kennedy MJ; Platte R; Davidson R; Ellis SD; Cole T; Bressac-de Paillerets B; Buecher B; Damiola F; Faivre L; Frenay M; Sinilnikova OM; Caron O; Giraud S; Mazoyer S; Bonadona V; Caux-Moncoutier V; Toloczko-Grabarek A; Gronwald J; Byrski T; Spurdle AB; Bonanni B; Zaffaroni D; Giannini G; Bernard L; Dolcetti R; Manoukian S; Arnold N; Engel C; Deissler H; Rhiem K; Niederacher D; Pendl H; Sutter C; Wappenschmidt B; Borg A; Mein B; Rantala J; Soller M; Nathanson KL; Domchek SM; Rodriguez GC; Salani R; Kaulich DG; Tea M-K; Paluch SS; Laitman Y; Skytte A-B; Kruse TA; Jensen UB; Robson M; Gerdes A-M; Ejlertsen B; Foretova L; Savage SA; Lesterm J; Soucy P; Kuchenbaecker KB; Olswold C; Cunningham JM; Slager S; Pankratz VS; Dicks E; Lakhani SR; Couch FJ; Hall P; Monteiro ANA; Gayther SA; Pharoah PDP; Reddel RR; Goode EL; Greene MH; Easton DF; Berchuck A; Antoniou AC; Chenevix-Trench G; Dunning AM
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2013;21(1):2-7
Developing a policy for paediatric biobanks: principles for good practice.
Hens K; Van El CE; Borry P; Cambon-Thomsen A; Cornel MC; Forzano F; Lucassen A; Patch C; Tranebjaerg L; Vermeulen E; Salvaterra E; Tibben A; Dierickx K; PPPC of the European Society of Human Genetics
Article: BREAST CANCER RESEARCH AND TREATMENT. 2012;136(1):295-302
Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers.
Stevens KN; Wang X; Fredericksen Z; Pankratz VS; Greene MH; Andrulis IL; Thomassen M; Caligo M; Swedish Breast Cancer Study, Sweden (SWE-BRCA); Nathanson KL; Jakubowska A; Osorio A; Hamann U; Godwin AK; Stoppa-Lyonnet D; Southey M; Buys SS; Singer CF; Hansen TVO; Arason A; Offit K; Piedmonte M; Montagna M; Imyanitov E; Tihomirova L; Sucheston L; Beattie M; HEreditary Breast and Ovarian Cancer Group Netherl; German Consortium for Hereditary Breast and Ovaria; Neuhausen SL; CONsorzio Studi ITaliani sui Tumori Ereditari Alla; Szabo CI; kConFab; Simard J; Spurdle AB; Healey S; Chen X; Rebbeck TR; Easton DF; Chenevix-Trench G; Antoniou AC; Couch FJ
Article: BMC MEDICAL GENOMICS. 2012;5:22
Relation between smoking history and gene expression profiles in lung adenocarcinomas
Staaf J; Jonsson G; Jonsson M; Karlsson A; Isaksson S; Salomonsson A; Pettersson HM; Soller M; Ewers S-B; Johansson L; Jonsson P; Planck M
Article: BRITISH JOURNAL OF CANCER. 2012;106(12):2016-2024
Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study
Jakubowska A; Rozkrut D; Antoniou A; Hamann U; Scott RJ; McGuffog L; Healy S; Sinilnikova OM; Rennert G; Lejbkowicz F; Flugelman A; Andrulis IL; Glendon G; Ozcelik H; Thomassen M; Paligo M; Aretini P; Kantala J; Aroer B; Von Wachenfeldt A; Liljegren A; Loman N; Herbst K; Kristoffersson U; Rosenquist R; Karlsson P; Stenmark-Askmalm M; Melin B; Nathanson KL; Domchek SM; Byrski T; Huzarski T; Gronwald J; Menkiszak J; Cybulski C; Serrano P; Osorio A; Cajal TR; Tsitlaidou M; Benitez J; Gilbert M; Rookus M; Aalfs CM; Kluijt I; Boessenkool-Pape JL; Meijers-Heijboer HEJ; Oosterwijk JC; van Asperen CJ; Blok MJ; Nelen MR; van den Ouweland AMW; Seynaeve C; van der Luijt RB; Devilee P; Easton DF; Peock S; Frost D; Platte R; Ellis SD; Fineberg E; Evans DG; Lalloo F; Eeles R; Jacobs C; Adlard J; Davidson R; Eccles D; Cole T; Cook J; Godwin A; Bove B; Stoppa-Lyonnet D; Caux-Moncoutier V; Belotti M; Tirapo C; Mazoyer S; Barjhoux L; Boutry-Kryza N; Pujol P; Coupier I; Peyrat J-P; Vennin P; Muller D; Fricker J-P; Venat-Bouvet L; Johannsson O; Isaacs C; Schmutzler R; Wappenschmidt B; Meindl A; Arnold N; Varon-Mateeva R; Niederacher D; Sutter C; Deissler H; Preisler-Adams S; Simard J; Soucy P; Durocher F; Chenevix-Trench G; Beesley J; Chen X; Rebbeck T; Couch F; Wang X; Lindor N; Fredericksen Z; Pankratz VS; Peterlongo P; Bonanni B; Fortuzzi S; Peissel B; Szabo C; Mai PL; Loud JT; Lubinski J
Article: AMERICAN JOURNAL OF MEDICAL GENETICS, PART A. 2012;158A(4):720-725
Screening of Congenital Heart Disease Patients Using Multiplex Ligation-Dependent Probe Amplification: Early Diagnosis of Syndromic Patients
Sorensen KM; El-Segaier M; Fernlund E; Errami A; Bouvagnet P; Nehme N; Steensberg J; Hjortdal V; Soller M; Behjati M; Werge T; Kirchoff M; Schouten J; Tommerup N; Andersen PS; Larsen LA
Article: CANCER EPIDEMIOLOGY, BIOMARKERS AND PREVENTION. 2012;21(4):645-657
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
Couch FJ; Gaudet MM; Antoniou AC; Ramus SJ; Kuchenbaecker KB; Soucy P; Beesley J; Chen X; Wang X; Kirchhoff T; McGuffog L; Barrowdale D; Lee A; Healey S; Sinilnikova OM; Andrulis IL; Ozcelik H; Mulligan AM; Thomassen M; Gerdes A-M; Jensen UB; Skytte A-B; Kruse TA; Caligo MA; von Wachenfeldt A; Barbany-Bustinza G; Loman N; Soller M; Ehrencrona H; Karlsson P; Nathanson KL; Rebbeck TR; Domchek SM; Jakubowska A; Lubinski J; Jaworska K; Durda K; Zlowocka E; Huzarski T; Byrski T; Gronwald J; Cybulski C; Gorski B; Osorio A; Duran M; Isabel Tejada M; Benitez J; Hamann U; Hogervorst FBL; van Os TA; van Leeuwen FE; Meijers-Heijboer HEJ; Wijnen J; Blok MJ; Kets M; Hooning MJ; Oldenburg RA; Ausems MGEM; Peock S; Frost D; Ellis SD; Platte R; Fineberg E; Evans DG; Jacobs C; Eeles RA; Adlard J; Davidson R; Eccles DM; Cole T; Cook J; Paterson J; Brewer C; Douglas F; Hodgson SV; Morrison PJ; Walker L; Porteous ME; Kennedy MJ; Side LE; Bove B; Godwin AK; Stoppa-Lyonnet D; Fassy-Colcombet M; Castera L; Cornelis F; Mazoyer S; Leone M; Boutry-Kryza N; Bressac-de Paillerets B; Caron O; Pujol P; Coupier I; Delnatte C; Akloul L; Lynch HT; Snyder CL; Buys SS; Daly MB; Terry M; Chung WK; John EM; Miron A; Southey MC; Hopper JL; Goldgar DE; Singer CF; Rappaport C; Tea M-KM; Fink-Retter A; Hansen TVO; Nielsen FC; Arason A; Vijai J; Shah S; Sarrel K; Robson ME; Piedmonte M; Phillips K; Basil J; Rubinstein WS; Boggess J; Wakeley K; Ewart-Toland A; Montagna M; Agata S; Imyanitov EN; Isaacs C; Janavicius R; Lazaro C; Blanco I; Feliubadalo L; Brunet J; Gayther SA; Pharoah PPD; Odunsi KO; Karlan BY; Walsh CS; Olah E; Teo SH; Ganz PA; Beattie MS; van Rensburg EJ; Dorfling CM; Diez O; Kwong A; Schmutzler RK; Wappenschmidt B; Engel C; Meindl A; Ditsch N; Arnold N; Heidemann S; Niederacher D; Preisler-Adams S; Gadzicki D; Varon-Mateeva R; Deissler H; Gehrig A; Sutter C; Kast K; Fiebig B; Heinritz W; Caldes T; de la Hoya M; Muranen TA; Nevanlinna H; Tischkowitz M; Spurdle AB; Neuhausen SL; Ding YC; Lindor NM; Fredericksen Z; Pankratz VS; Peterlongo P; Manoukian S; Peissel B; Zaffaroni D; Barile M; Bernard L; Viel A; Giannini G; Varesco L; Radice P; Greene MH; Mai PL; Easton DF; Chenevix-Trench G; Offit K; Simard J
Article: HUMAN MUTATION. 2012;33(4):690-702
Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers
Ramus SJ; Antoniou AC; Kuchenbaecker KB; Soucy P; Beesley J; Chen X; McGuffog L; Sinilnikova OM; Healey S; Barrowdale D; Lee A; Thomassen M
Article: HUMAN MOLECULAR GENETICS. 2011;20(23):4732-4747
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
Cox DG; Simard J; Sinnett D; Hamdi Y; Soucy P; Ouimet M; Barjhoux L; Verny-Pierre C; McGuffog L; Healey S; Szabo C; Greene MH; Mai PL; Andrulis IL; Thomassen M; Gerdes A-M; Caligo MA; Friedman E; Laitman Y; Kaufman B; Paluch SS; Borg A; Karlsson P; Askmalm MS; Bustinza GB; Nathanson KL; Domchek SM; Rebbeck TR; Benitez J; Hamann U; Rookus MA; van den Ouweland AMW; Ausems MGEM; Aalfs CM; van Asperen CJ; Devilee P; Gille HJJP; Peock S; Frost D; Evans DG; Eeles R; Izatt L; Adlard J; Paterson J; Eason J; Godwin AK; Remon M-A; Moncoutier V; Gauthier-Villars M; Lasset C; Giraud S; Hardouin A; Berthet P; Sobol H; Eisinger F; de Paillerets BB; Caron O; Delnatte C; Goldgar D; Miron A; Ozcelik H; Buys S; Southey MC; Terry MB; Singer CF; Dressler A-C; Tea M-K; Hansen TVO; Johannsson O; Piedmonte M; Rodriguez GC; Basil JB; Blank S; Toland AE; Montagna M; Isaacs C; Blanco I; Gayther SA; Moysich KB; Schmutzler RK; Wappenschmidt B; Engel C; Meindl A; Ditsch N; Arnold N; Niederacher D; Sutter C; Gadzicki D; Fiebig B; Caldes T; Laframboise R; Nevanlinna H; Chen X; Beesley J; Spurdle AB; Neuhausen SL; Ding YC; Couch FJ; Wang X; Peterlongo P; Manoukian S; Bernard L; Radice P; Easton DF; Chenevix-Trench G; Antoniou AC; Stoppa-Lyonnet D; Mazoyer S; Sinilnikova OM
Article: HUMAN MUTATION. 2011;32(7):723-728
Mutation Update for the PORCN Gene
Lombardi MP; Bulk S; Celli J; Lampe A; Gabbett MT; Ousager LB; van der Smagt JJ; Soller M; Stattin E-L; Mannens MAMM; Smigiel R; Hennekam RC
Article: BREAST CANCER RESEARCH. 2011;13(6):R110
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
Mulligan AM; Couch FJ; Barrowdale D; Domchek SM; Eccles D; Nevanlinna H; Ramus SJ; Robson M; Sherman M; Spurdle AB; Wappenschmidt B; Lee A; McGuffog L; Healey S; Sinilnikova OM; Janavicius R; Hansen TVO; Nielsen FC; Ejlertsen B; Osorio A; Munoz-Repeto I; Duran M; Godino J; Pertesi M; Benitez J; Peterlongo P; Manoukian S; Peissel B; Zaffaroni D; Cattaneo E; Bonanni B; Viel A; Pasini B; Papi L; Ottini L; Savarese A; Bernard L; Radice P; Hamann U; Verheus M; Meijers-Heijboer HEJ; Wijnen J; Garcia EBG; Nelen MR; Kets CM; Seynaeve C; Tilanus-Linthorst MMA; van der Luijt RB; van Os T; Rookus M; Frost D; Jones JL; Evans DG; Lalloo F; Eeles R; Izatt L; Adlard J; Davidson R; Cook J; Donaldson A; Dorkins H; Gregory H; Eason J; Houghton C; Barwell J; Side LE; McCann E; Murray A; Peock S; Godwin AK; Schmutzler RK; Rhiem K; Engel C; Meindl A; Ruehl I; Arnold N; Niederacher D; Sutter C; Deissler H; Gadzicki D; Kast K; Preisler-Adams S; Varon-Mateeva R; Schoenbuchner I; Fiebig B; Heinritz W; Schaefer D; Gevensleben H; Caux-Moncoutier V; Fassy-Colcombet M; Cornelis F; Mazoyer S; Leone M; Boutry-Kryza N; Hardouin A; Berthet P; Muller D; Fricker J-P; Mortemousque I; Pujol P; Coupier I; Lebrun M; Kientz C; Longy M; Sevenet N; Stoppa-Lyonnet D; Isaacs C; Caldes T; de la Hoya M; Heikkinen T; Aittomaki K; Blanco I; Lazaro C; Barkardottir RB; Soucy P; Dumont M; Simard J; Montagna M; Tognazzo S; D'Andrea E; Fox S; Yan M; Rebbeck T; Olopade OI; Weitzel JN; Lynch HT; Ganz PA; Tomlinson GE; Wang X; Fredericksen Z; Pankratz VS; Lindor NM; Szabo C; Offit K; Sakr R; Gaudet M; Bhatia J; Kauff N; Singer CF; Tea M-K; Gschwantler-Kaulich D; Fink-Retter A; Mai PL; Greene MH; Imyanitov E; O'Malley FP; Ozcelik H; Glendon G; Toland AE; Gerdes A-M; Thomassen M; Kruse TA; Jensen UB; Skytte A-B; Caligo MA; Soller M; Henriksson K; Wachenfeldt VA; Arver B; Stenmark-Askmalm M; Karlsson P; Ding YC; Neuhausen SL; Beattie M; Pharoah PDP; Moysich KB; Nathanson KL; Karlan BY; Gross J; John EM; Daly MB; Buys SM; Southey MC; Hopper JL; Terry MB; Chung W; Miron AF; Goldgar D; Chenevix-Trench G; Easton DF; Andrulis IL; Antoniou AC
Article: HUMAN MUTATION. 2010;31(10):1142-1154
Molecular Analysis Expands the Spectrum of Phenotypes Associated with GLI3 Mutations
Johnston JJ; Sapp JC; Turner JT; Amor D; Aftimos S; Aleck KA; Bocian M; Bodurtha JN; Cox GF; Curry CJ; Day R; Donnai D; Field M; Fujiwara I; Gabbett M; Gal M; Graham JMJ; Hedera P; Hennekam RCM; Hersh JH; Hopkin RJ; Kayserili H; Kidd AMJ; Kimonis V; Lin AE; Lynch SA; Maisenbacher M; Mansour S; McGaughran J; Mehta L; Murphy H; Raygada M; Robin NH; Rope AF; Rosenbaum KN; Schaefer GB; Shealy A; Smith W; Soller M; Sommer A; Stalker HJ; Steiner B; Stephan MJ; Tilstra D; Tomkins S; Trapane P; Tsai AC-H; Van Allen MI; Vasudevan PC; Zabel B; Zunich J; Black GCM; Biesecker LG
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2010;18(9):972-977
Genetic education and the challenge of genomic medicine: development of core competences to support preparation of health professionals in Europe.
Skirton H; Lewis C; Kent A; Coviello DA; Members of Eurogentest Unit 6 and ESHG Education C
Article: BMC CANCER. 2010;10:385
HIF1α isoforms in benign and malignant prostate tissue and their correlation to neuroendocrine differentiation
Monsef N; Soller M; Panagopoulos I; Abrahamsson PA
Article: OBESITY. 2010;18(3):580-587
dup(19)(q12q13.2): Array-based Genotype-Phenotype Correlation of a New Possibly Obesity-related Syndrome
Davidsson J; Jahnke K; Forsgren M; Collin A; Soller M
Article: PUBLIC HEALTH GENOMICS. 2010;13(7-8):396-405
How to Handle Genetic Information: A Comparison of Attitudes among Patients and the General Population
Wolff K; Brun W; Kvale G; Ehrencrona H; Soller M; Nordin K
Article: PROSTATE. 2009;69(9):909-916
The Expression of Pluripotency Marker Oct 3/4 in Prostate Cancer and Benign Prostate Hyperplasia
Monsef N; Soller M; Isaksson M; Abrahamsson PA; Panagopoulos I
Article: EPILEPSY RESEARCH. 2008;81(1):69-79
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
Davidsson J; Collin A; Olsson ME; Lundgren J; Soller M
Article: CLINICAL GENETICS. 2008;74(1):31-38
CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome
Wincent J; Holmberg E; Stromland K; Soller M; Mirzaei L; Djureinovic T; Robinson KL; Anderlid BM; Schoumans J
Article: BMC MEDICAL GENETICS. 2008;9:2
Array based characterization of a terminal deletion involving chromosome subband 15q26.2:: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay
Davidsson J; Collin A; Bjorkhem G; Soller M
Article: CANCER GENETICS. 2007;173(1):75-80
Cytogenetic findings in pediatric renal cell carcinoma.
Soller MJ; Kullendorff C-M; Békássy AN; Alumets J; Mertens F
Article: GENETIC TESTING AND MOLECULAR BIOMARKERS. 2007;11(2):183-186
Discrepancies between estimated and perceived risk of cancer among individuals with hereditary nonpolyposis colorectal cancer
Domanska K; Nilbert M; Soller M; Silfverberg B; Carlsson C
Article: BMC CANCER. 2006;6:69
Midline carcinoma with t(15;19) and BRD4-NUT fusion oncogene in a 30-year-old female with response to docetaxel and radiotherapy -: art. no. 69
Engleson J; Soller M; Panagopoulos I; Dahlén A; Dictor M; Jerkeman M
Article: CANCER GENETICS. 2004;153(1):1-9
Dissecting karyotypic patterns in renal cell carcinoma:: an analysis of the accumulated cytogenetic data
Höglund M; Gisselsson D; Soller M; Hansen GB; Elfving P; Mitelman F
Article: GENES CHROMOSOMES AND CANCER. 2004;40(3):172-178
A model for karyotypic evolution in testicular germ cell tumors
Frigyesi A; Gisselsson D; Hansen GB; Soller M; Mitelman F; Höglund M
Article: CANCER GENETICS. 2003;140(1):82-87
Cytogenetic findings and clinical course in a consecutive series of Wilms tumors
Kullendorff CM; Soller M; Wiebe T; Mertens F
Article: CANCER GENETICS. 1995;81(1):46-55
CYTOGENETIC ANALYSIS OF SHORT-TERM CULTURED SQUAMOUS-CELL CARCINOMAS OF THE LUNG
JOHANSSON M; JIN YS; MANDAHL N; HAMBRAEUS G; JOHANSSON L; MITELMAN F; HEIM S
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Review: GYNECOLOGIC ONCOLOGY. 2016;141(2):386-401
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
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Corrigendum: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015;23(11):1592-1591
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening (vol 23, pg 1438, 2015)
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Benchmarks for Cystic Fibrosis carrier screening: A European consensus document
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False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite probe (D18Z1) to chromosome 2
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Letter: HAEMOPHILIA. 2008;14(4):846-848
Female haemophilia A caused by skewed X inactivation.
Knobe KE; Sjörin E; Soller MJ; Liljebjörn H; Ljung RCR
Meeting abstract: EUROPEAN UROLOGY OPEN SCIENCE. 2006;5(14):789
High frequency of the TMPRSS2/ERG fusion gene in prostate cancer
Soller W; Soller JM; Isaksson M; Elfving P; Abrahamsson PA; Lundgren R; Panagopoulos I
Letter: GENES CHROMOSOMES AND CANCER. 2006;45(7):717-719
Confirmation of the high frequency of the TMPRSS2/ERG fusion gene in prostate cancer.
Soller MJ; Isaksson M; Elfving P; Soller W; Lundgren R; Panagopoulos I
Letter: FAMILIAL CANCER. 2005;4(2):191-194
The BRCA1 exon 13 duplication in the Swedish population
Kremeyer B; Soller M; Lagerstedt K; Maguire P; Mazoyer S; Nordling M; Wahlström J; Lindblom A
Letter: CANCER GENETICS. 1995;80(1):85-86
TRANSLOCATION-11-19 IN A MUCOEPIDERMOID TUMOR OF THE LUNG
JOHANSSON M; MANDAHL N; JOHANSSON L; HAMBRAEUS G; MITELMAN F; HEIM S

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Anknuten till Forskning, Molekylär medicin och kirurgi, Karolinska Institutet, 2023-2026

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Marlene Ek, 2021
Emma Ehn, 2019

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