Maria Johansson Soller

Publications
Public outreach and news

Articles

Article: SCIENTIFIC REPORTS. 2023;13(1):6904

The cost-effectiveness of whole genome sequencing in neurodevelopmental disorders.

Runheim H; Pettersson M; Hammarsjö A; Nordgren A; Henriksson M; Lindstrand A; Levin L-Å; 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; Björck E; Carlsten J; Eisfeldt J; Grigelioniene G; Gustavsson P; Hammarsjö A; Helgadóttir HT; Hellström-Pigg M; Kuchinskaya E; Lagerstedt-Robinson K; Levin L-Å; Lieden A; Lindelöf H; Malmgren H; Nilsson D; Svensson E; Paucar M; Sahlin E; Tesi B; Tham E; Winberg J; Winerdal M; Wincent J; Johansson Soller M; Pettersson M; Nordgren A
Article: PLOS ONE. 2022;17(2):e0264056

A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population.

Lagerstedt-Robinson K; Baranowska Körberg I; Tsiaprazis S; Björck E; Tham E; Poluha A; Hellström Pigg M; Paulsson-Karlsson Y; Nordenskjöld M; Johansson-Soller M; Aravidis 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: 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.

Rodríguez-Palmero A; Boerrigter MM; Gómez-Andrés D; Aldinger KA; Marcos-Alcalde Í; Popp B; Everman DB; Lovgren AK; Arpin S; Bahrambeigi V; Beunders G; Bisgaard A-M; Bjerregaard VA; Bruel A-L; Challman TD; Cogné B; Coubes C; de Man SA; Denommé-Pichon A-S; Dye TJ; Elmslie F; Feuk L; García-Miñaúr 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; Müller AJ; O'Leary M; Pacio-Míguez 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; Schlüter A; Schönewolf-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; Waldmüller S; Whiting S; Zweier C; Prada CE; de Vries BBA; Dobyns WB; Reiter SF; Gómez-Puertas P; Pujol A; Tümer 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; Björck E; Bruhn H; Eisfeldt J; Freyer C; Grigelioniene G; Gustavsson P; Hammarsjö A; Hellström-Pigg M; Iwarsson E; Jemt A; Laaksonen M; Enoksson SL; Malmgren H; Naess K; Nordenskjöld M; Oscarson M; Pettersson M; Rasi C; Rosenbaum A; Sahlin E; Sardh E; Stödberg T; Tesi B; Tham E; Thonberg H; Töhönen V; von Döbeln U; Vassiliou D; Vonlanthen S; Wikström A-C; Wincent J; Winqvist O; Wredenberg A; Ygberg S; Zetterström 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; Truvé 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 Á; Patch C; Radojkovic D; Rial-Sebbag E; Sheppard MN; Tassé A-M; Temel SG; Sajantila A; Basso C; Wilde AAM; Cornel MC; on behalf of European Society of Human Genetics, E
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; Hammarsjö A; Georgii-Hemming P; Iwarsson E; Johansson-Soller M; Lagerstedt-Robinson K; Lieden A; Magnusson M; Martin M; Malmgren H; Nordenskjöld 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 & RELATED DISORDERS. 2019;66:158-165

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

Puschmann A; Jiménez-Ferrer I; Lundblad-Andersson E; Mårtensson E; Hansson O; Odin P; Widner H; Brolin K; Mzezewa R; Kristensen J; Soller M; Rödström 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; Tomašić N; Kallijärvi J; Purhonen J; Elmér 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; Billette de Villemeur T; 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; Häckl B; von Stülpnagel C; Kluger G; Møller RS; Pal D; Jonson T; Soller M; Verbeek NE; van Haelst MM; de Kovel C; Koeleman B; Monroe G; van Haaften G; DDD Study; Attié-Bitach T; Boutaud L; Héron 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; Haikal 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; Tranebjærg L; van El CG; Cornel MC; European Society of Human Genetics; American Society of Human Genetics
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; Victoria Hodgson S; Howard HC; John J; Kääriäinen H; Kayserili H; Kent A; Koerber F; Kristoffersson U; Kroese M; Lewis C; Marckmann G; Meyer P; Pfeufer A; Schmidtke J; Skirton H; Tranebjærg L; Rogowski WH; EuroGentest and ESHG/PPPC Priority Consortium
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.

Schlögel MJ; Mendola A; Fastré 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; Jønson 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; EMBRACE; Godwin AK; Schmutzler RK; Meindl A; Engel C; Sutter C; Sinilnikova OM; GEMO Study Collaborators; 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; Aittomäki K; Nevanlinna H; Collée JM; Rookus MA; Oosterwijk JC; Breast Cancer Family Registry; Tihomirova L; Tung N; Hamann U; Isaccs C; Tischkowitz M; Imyanitov EN; Caligo MA; Campbell IG; Hogervorst FBL; HEBON; Olah E; Diez O; Blanco I; Brunet J; Lazaro C; Pujana MA; Jakubowska A; Gronwald J; Lubinski J; Sukiennicki G; Barkardottir RB; Plante M; Simard J; Soucy P; Montagna M; Tognazzo S; Teixeira MR; KConFab Investigators; 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; Australian Cancer Study (Ovarian Cancer Investigat; Australian Ovarian Cancer Study Group; 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; Dürst M; Hillemanns P; Dörk 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; Consortium of Investigators of Modifiers of BRCA1
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; de Garibay GR; Librado P; Sánchez-Gracia A; Rozas J; Bonifaci N; McGuffog L; Pankratz VS; Islam A; Mateo F; Berenguer A; Petit A; Català I; Brunet J; Feliubadaló L; Tornero E; Benítez J; Osorio A; Ramón y Cajal T; Nevanlinna H; Aittomäki 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; Díez O; Hansen TV; Jønson L; Gerdes A-M; Ejlertsen B; de la Hoya M; Caldés 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; BCFR; 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; SWE-BRCA; Liljegren A; Rantala J; Stenmark-Askmalm M; Loman N; Imyanitov EN; Hamann U; kConFab Investigators; Spurdle AB; Healey S; Weitzel JN; Herzog J; Margileth D; Gorrini C; Esteller M; Gómez A; Sayols S; Vidal E; Heyn H; GEMO; Stoppa-Lyonnet D; Léoné 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; Lázaro C; Easton DF; Offit K; Chenevix-Trench G; Couch FJ; Antoniou AC; Pujana MA
Article: PARKINSONISM & 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; Gellera C; Caldarazzo S; Duno M; Soller M; Puschmann A
Article: PARKINSONISM & RELATED DISORDERS. 2014;20(7):748-754

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

Wictorin K; Brådvik B; Nilsson K; Soller M; van Westen D; Bynke G; Bauer P; Schöls 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; Australian Cancer Study; Australian Ovarian Cancer Study; Kathleen Cuningham Foundation Consortium for Resea; Gene Environment Interaction and Breast Cancer (GE; Swedish Breast Cancer Study (SWE-BRCA); Hereditary Breast and Ovarian Cancer Research Grou; Epidemiological study of BRCA1 & BRCA2 Mutation Ca; Genetic Modifiers of Cancer Risk in BRCA1/2 Mutati; Vergote I; Lambrechts S; Despierre E; Risch HA; González-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; Guénel 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; Dürst M; Devilee P; Runnebaum I; Jakubowska A; Lubinski J; Mannermaa A; Butzow R; Bogdanova NV; Dörk 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; Høgdall 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; Orlow I; Blomqvist C; Rodriguez-Rodriguez L; Aittomäki 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; Truong T; Massuger LFAG; Benitez J; Pejovic T; Perez JIA; 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; Le Marchand L; Yang HP; Mulligan AM; Glendon G; Engelholm SA; Knight JA; Høgdall 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; Müller H; Arndt V; Labrèche 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; Brüning T; Pike MC; Ko Y-D; Lissowska J; Figueroa J; Kupryjanczyk J; Chanock SJ; Dansonka-Mieszkowska A; Jukkola-Vuorinen A; Rzepecka IK; Pylkäs 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; Ikram 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 Roozendaal KEP; Meijers-Heijboer H; Collée 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; Plendl H; Sutter C; Wappenschmidt B; Borg A; Melin 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; Lester 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: BMC MEDICAL GENOMICS. 2012;5:22

Relation between smoking history and gene expression profiles in lung adenocarcinomas.

Staaf J; Jönsson G; Jönsson M; Karlsson A; Isaksson S; Salomonsson A; Pettersson HM; Soller M; Ewers S-B; Johansson L; Jönsson P; Planck M
Article: CANCER EPIDEMIOLOGY BIOMARKERS & 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; OCGN; 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; SWE-BRCA; Nathanson KL; Rebbeck TR; Domchek SM; Jakubowska A; Lubinski J; Jaworska K; Durda K; Zlowocka E; Huzarski T; Byrski T; Gronwald J; Cybulski C; Górski B; Osorio A; Durán M; Tejada MI; Benitez J; Hamann U; Hogervorst FBL; HEBON; 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; EMBRACE; Bove B; Godwin AK; Stoppa-Lyonnet D; GEMO Study Collaborators; Fassy-Colcombet M; Castera L; Cornelis F; Mazoyer S; Léoné 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 MD; 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; kConFab investigators; Offit K; Simard J; Consortium of Investigators of Modifiers of BRCA1/
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.

Sørensen 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: 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 TV; Nielsen FC; Ejlertsen B; Osorio A; Muñoz-Repeto I; Durán M; Godino J; Pertesi M; Benítez 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; Gómez García EB; 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; Schäfer D; Gevensleben H; Caux-Moncoutier V; Fassy-Colcombet M; Cornelis F; Mazoyer S; Léoné 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; Aittomäki 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 O; 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; Breast Cancer Family Registry; EMBRACE; GEMO Study Collaborators; HEBON; kConFab Investigators; Ontario Cancer Genetics Network; SWE-BRCA; CIMBA
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 JM; 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: BMC CANCER. 2010;10:385

HIF1alpha 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; Strömland K; Soller M; Mirzaei L; Djureinovic T; Robinson K; Anderlid B; 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; Björkhem 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.

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 & 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 Y; Mandahl N; Hambraeus G; Johansson L; Mitelman F; Heim S
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Letter: NATURE MEDICINE. 2022;28(10):1980-1982

Implementing precision medicine in a regionally organized healthcare system in Sweden.

Fioretos T; Wirta V; Cavelier L; Berglund E; Friedman M; Akhras M; Botling J; Ehrencrona H; Engstrand L; Helenius G; Fagerqvist T; Gisselsson D; Gruvberger-Saal S; Gyllensten U; Heidenblad M; Höglund K; Jacobsson B; Johansson M; Johansson Å; Soller MJ; Landström M; Larsson P; Levin L-Å; Lindstrand A; Lovmar L; Lyander A; Melin M; Nordgren A; Nordmark G; Mölling P; Palmqvist L; Palmqvist R; Repsilber D; Sikora P; Stenmark B; Söderkvist P; Stranneheim H; Strid T; Wheelock CE; Wadelius M; Wedell A; Edsjö A; Rosenquist R
Editorial comment: NEUROMUSCULAR DISORDERS. 2022;32(1):86-97

259th ENMC international workshop: Anaesthesia and neuromuscular disorders 11 December, 2020 and 28-29 May, 2021.

van den Bersselaar LR; Riazi S; Snoeck M; Jungbluth H; Voermans NC; Anaesthesia and Neuromuscular Disorders Working Gr
Review: AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS. 2019;180(8):523-532

Psychiatric genetic counseling: A mapping exercise.

Moldovan R; McGhee KA; Coviello D; Hamang A; Inglis A; Ingvoldstad Malmgren C; Johansson-Soller M; Laurino M; Meiser B; Murphy L; Paneque M; Papsuev O; Pawlak J; Rovira Moreno E; Serra-Juhe C; Shkedi-Rafid S; Laing N; Voelckel M-A; Watson M; Austin JC
Review: GYNECOLOGIC ONCOLOGY. 2016;141(2):386-401

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

Ovarian Cancer Association Consortium, Breast Canc; Hollestelle A; van der Baan FH; Berchuck A; Johnatty SE; Aben KK; Agnarsson BA; Aittomäki K; Alducci E; Andrulis IL; Anton-Culver H; Antonenkova NN; Antoniou AC; Apicella C; Arndt V; Arnold N; Arun BK; Arver B; Ashworth A; Australian Ovarian Cancer Study Group; Baglietto L; Balleine R; Bandera EV; Barrowdale D; Bean YT; Beckmann L; Beckmann MW; Benitez J; Berger A; Berger R; Beuselinck B; Bisogna M; Bjorge L; Blomqvist C; Bogdanova NV; Bojesen A; Bojesen SE; Bolla MK; Bonanni B; Brand JS; Brauch H; Breast Cancer Family Register; Brenner H; Brinton L; Brooks-Wilson A; Bruinsma F; Brunet J; Brüning T; Budzilowska A; Bunker CH; Burwinkel B; Butzow R; Buys SS; Caligo MA; Campbell I; Carter J; Chang-Claude J; Chanock SJ; Claes KBM; Collée JM; Cook LS; Couch FJ; Cox A; Cramer D; Cross SS; Cunningham JM; Cybulski C; Czene K; Damiola F; Dansonka-Mieszkowska A; Darabi H; de la Hoya M; deFazio A; Dennis J; Devilee P; Dicks EM; Diez O; Doherty JA; Domchek SM; Dorfling CM; Dörk T; Silva IDS; du Bois A; Dumont M; Dunning AM; Duran M; Easton DF; Eccles D; Edwards RP; Ehrencrona H; Ejlertsen B; Ekici AB; Ellis SD; EMBRACE; Engel C; Eriksson M; Fasching PA; Feliubadalo L; Figueroa J; Flesch-Janys D; Fletcher O; Fontaine A; Fortuzzi S; Fostira F; Fridley BL; Friebel T; Friedman E; Friel G; Frost D; Garber J; García-Closas M; Gayther SA; GEMO Study Collaborators; GENICA Network; Gentry-Maharaj A; Gerdes A-M; Giles GG; Glasspool R; Glendon G; Godwin AK; Goodman MT; Gore M; Greene MH; Grip M; Gronwald J; Gschwantler Kaulich D; Guénel P; Guzman SR; Haeberle L; Haiman CA; Hall P; Halverson SL; Hamann U; Hansen TVO; Harter P; Hartikainen JM; Healey S; HEBON; Hein A; Heitz F; Henderson BE; Herzog J; T Hildebrandt MA; Høgdall CK; Høgdall E; Hogervorst FBL; Hopper JL; Humphreys K; Huzarski T; Imyanitov EN; Isaacs C; Jakubowska A; Janavicius R; Jaworska K; Jensen A; Jensen UB; Johnson N; Jukkola-Vuorinen A; Kabisch M; Karlan BY; Kataja V; Kauff N; KConFab Investigators; Kelemen LE; Kerin MJ; Kiemeney LA; Kjaer SK; Knight JA; Knol-Bout JP; Konstantopoulou I; Kosma V-M; Krakstad C; Kristensen V; Kuchenbaecker KB; Kupryjanczyk J; Laitman Y; Lambrechts D; Lambrechts S; Larson MC; Lasa A; Laurent-Puig P; Lazaro C; Le ND; Le Marchand L; Leminen A; Lester J; Levine DA; Li J; Liang D; Lindblom A; Lindor N; Lissowska J; Long J; Lu KH; Lubinski J; Lundvall L; Lurie G; Mai PL; Mannermaa A; Margolin S; Mariette F; Marme F; Martens JWM; Massuger LFAG; Maugard C; Mazoyer S; McGuffog L; McGuire V; McLean C; McNeish I; Meindl A; Menegaux F; Menéndez P; Menkiszak J; Menon U; Mensenkamp AR; Miller N; Milne RL; Modugno F; Montagna M; Moysich KB; Müller H; Mulligan AM; Muranen TA; Narod SA; Nathanson KL; Ness RB; Neuhausen SL; Nevanlinna H; Neven P; Nielsen FC; Nielsen SF; Nordestgaard BG; Nussbaum RL; Odunsi K; Offit K; Olah E; Olopade OI; Olson JE; Olson SH; Oosterwijk JC; Orlow I; Orr N; Orsulic S; Osorio A; Ottini L; Paul J; Pearce CL; Pedersen IS; Peissel B; Pejovic T; Pelttari LM; Perkins J; Permuth-Wey J; Peterlongo P; Peto J; Phelan CM; Phillips K-A; Piedmonte M; Pike MC; Platte R; Plisiecka-Halasa J; Poole EM; Poppe B; Pylkäs K; Radice P; Ramus SJ; Rebbeck TR; Reed MWR; Rennert G; Risch HA; Robson M; Rodriguez GC; Romero A; Rossing MA; Rothstein JH; Rudolph A; Runnebaum I; Salani R; Salvesen HB; Sawyer EJ; Schildkraut JM; Schmidt MK; Schmutzler RK; Schneeweiss A; Schoemaker MJ; Schrauder MG; Schumacher F; Schwaab I; Scuvera G; Sellers TA; Severi G; Seynaeve CM; Shah M; Shrubsole M; Siddiqui N; Sieh W; Simard J; Singer CF; Sinilnikova OM; Smeets D; Sohn C; Soller M; Song H; Soucy P; Southey MC; Stegmaier C; Stoppa-Lyonnet D; Sucheston L; SWE-BRCA; Swerdlow A; Tangen IL; Tea M-K; Teixeira MR; Terry KL; Terry MB; Thomassen M; Thompson PJ; Tihomirova L; Tischkowitz M; Toland AE; Tollenaar RAEM; Tomlinson I; Torres D; Truong T; Tsimiklis H; Tung N; Tworoger SS; Tyrer JP; Vachon CM; Van 't Veer LJ; van Altena AM; Van Asperen CJ; van den Berg D; van den Ouweland AMW; van Doorn HC; Van Nieuwenhuysen E; van Rensburg EJ; Vergote I; Verhoef S; Vierkant RA; Vijai J; Vitonis AF; von Wachenfeldt A; Walsh C; Wang Q; Wang-Gohrke S; Wappenschmidt B; Weischer M; Weitzel JN; Weltens C; Wentzensen N; Whittemore AS; Wilkens LR; Winqvist R; Wu AH; Wu X; Yang HP; Zaffaroni D; Pilar Zamora M; Zheng W; Ziogas A; Chenevix-Trench G; Pharoah PDP; Rookus MA; Hooning MJ; Goode EL
Corrigendum: EUROPEAN JOURNAL OF HUMAN GENETICS. 2015;23(11):1592

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; Tranebjærg L; van El CG; Cornel MC
Review: JOURNAL OF CYSTIC FIBROSIS. 2010;9(3):165-178

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

Castellani C; Macek M; Cassiman J-J; Duff A; Massie J; ten Kate LP; Barton D; Cutting G; Dallapiccola B; Dequeker E; Girodon E; Grody W; Highsmith EW; Kääriäinen H; Kruip S; Morris M; Pignatti PF; Pypops U; Schwarz M; Soller M; Stuhrman M; Cuppens H
Letter: PRENATAL DIAGNOSIS. 2009;29(13):1279-1281

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

Collin A; Sladkevicius P; Soller M
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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