Teresita Díaz de Ståhl

Publikationer
CV
Populärvetenskap och samverkan

Artiklar

Article: AMERICAN JOURNAL OF CASE REPORTS. 2024;25:e945715
Pediatric Soft Tissue Sarcoma in Limb-Girdle Muscular Dystrophy: Molecular Findings and Clinical Implications
Maya-Gonzalez C; De Stahl TD; Wessman S; Taylan F; Tesi B; Lagerstedt-Robinson K; Tettamanti G; Dukic M; Poluha A; Ljungman G; Nordgren A
Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2024;194(12):e63812
Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature
Maya-Gonzalez C; Delgado-Vega AM; Taylan F; Robinson KL; Hansson L; Pal N; Fagman H; Puls F; Wessman S; Stenman J; Georgantzi K; Fransson S; De Stahl TD; Ek T; Palmer R; Tesi B; Kogner P; Martinsson T; Nordgren A
Article: LANCET REGIONAL HEALTH-EUROPE. 2024;39:100881
Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors - a nationwide, prospective Swedish study
Tesi B; Robinson KL; Abel F; Stahl TDD; Orrsjoe S; Poluha A; Hellberg M; Wessman S; Samuelsson S; Frisk T; Vogt H; Henning K; Sabel M; Ek T; Pal N; Nyman P; Giraud G; Wille J; Pronk CJ; Noren-Nystroem U; Borssen M; Fili M; Stalhammar G; Herold N; Tettamanti G; Maya-Gonzalez C; Arvidsson L; Rosen A; Ekholm K; Kuchinskaya E; Hallbeck A-L; Nordling M; Palmebaeck P; Kogner P; Smoler GK; Laehteenmaeki P; Fransso S; Martinsson T; Shamik A; Mertens F; Rosenquist R; Wirta V; Tham E; Grillner P; Sandgren J; Ljungman G; Gisselsson D; Taylan F; Nordgren A
Article: NEURO-ONCOLOGY ADVANCES. 2024;6(1):vdae008
The potential of liquid biopsy for detection of the KIAA1549-BRAF fusion in circulating tumor DNA from children with pilocytic astrocytoma
Krynina O; de Stahl TD; Jylhae C; Arthur C; Giraud G; Nyman P; Fritzberg A; Sandgren J; Tham E; Sandvik U
Article: INVESTIGATIONAL NEW DRUGS. 2023;41(5):688-698
Cytotoxicity of poly-guanidine in medulloblastoma cell lines
Gallo-Oller G; de Stahl TD; Alaiya A; Nilsson S; Holmberg AR; Marquez-Mendez M
Article: FRONTIERS IN MEDICINE. 2023;10:1172565
Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation
Maya-Gonzalez C; Wessman S; Lagerstedt-Robinson K; Taylan F; Tesi B; Kuchinskaya E; McCluggage WG; Poluha A; Holm S; Nergardh R; De Stahl TD; Hoybye C; Tettamanti G; Delgado-Vega AM; Skarin Nordenvall A; Nordgren A
Article: JCO PRECISION ONCOLOGY. 2023;7:e2300039
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer
Wadensten E; Wessman S; Abel F; De Stahl TD; Tesi B; Pietras CO; Arvidsson L; Taylan F; Fransson S; Vogt H; Poluha A; Pradhananga S; Hellberg M; Lagerstedt-Robinson K; Raj Somarajan P; Samuelsson S; Orrsjo S; Maqbool K; Henning K; Strid T; Ek T; Fagman H; Bontell TO; Martinsson T; Puls F; Kogner P; Wirta V; Pronk CJ; Wille J; Rosenquist R; Nister M; Mertens F; Sabel M; Noren-Nystrom U; Grillner P; Nordgren A; Ljungman G; Sandgren J; Gisselsson D
Article: JOURNAL OF TRANSLATIONAL MEDICINE. 2023;21(1):342
The Swedish childhood tumor biobank: systematic collection and molecular characterization of all pediatric CNS and other solid tumors in Sweden
de Stahl TD; Shamikh A; Mayrhofer M; Juhos S; Basmaci E; Prochazka G; Garcia M; Somarajan PR; Zielinska-Chomej K; Illies C; Ora I; Siesjo P; Sandstrom P-E; Stenman J; Sabel M; Gustavsson B; Kogner P; Pfeifer S; Ljungman G; Sandgren J; Nister M
Article: CANCERS. 2023;15(7):1972
Simultaneous Ultra-Sensitive Detection of Structural and Single Nucleotide Variants Using Multiplex Droplet Digital PCR in Liquid Biopsies from Children with Medulloblastoma
Arthur C; Jylha C; de Stahl TD; Shamikh A; Sandgren J; Rosenquist R; Nordenskjold M; Harila A; Barbany G; Sandvik U; Tham E
Article: NATURE. 2022;608(7922):360-367
Spatially resolved clonal copy number alterations in benign and malignant tissue
Erickson A; He M; Berglund E; Marklund M; Mirzazadeh R; Schultz N; Kvastad L; Andersson A; Bergenstrahle L; Bergenstrahle J; Larsson L; Galicia LA; Shamikh A; Basmaci E; De Stahl TD; Rajakumar T; Doultsinos D; Thrane K; Ji AL; Khavari PA; Tarish F; Tanoglidi A; Maaskola J; Colling R; Mirtti T; Hamdy FC; Woodcock DJ; Helleday T; Mills IG; Lamb AD; Lundeberg J
Article: NEURO-ONCOLOGY ADVANCES. 2020;2(1):vdaa061
Identification of functionally distinct and interacting cancer cell subpopulations from glioblastoma with intratumoral genetic heterogeneity
Guo M; van Vliet M; Zhao J; de Stahl TD; Lindstrom MS; Cheng H; Heller S; Nister M; Hagerstrand D
Article: F1000RESEARCH. 2020;9:63
Sarek: A portable workflow for whole-genome sequencing analysis of germline and somatic variants.
Garcia M; Juhos S; Larsson M; Olason PI; Martin M; Eisfeldt J; DiLorenzo S; Sandgren J; Díaz De Ståhl T; Ewels P; Wirta V; Nistér M; Käller M; Nystedt B
Article: SPRINGERPLUS. 2016;5(1):1861
Identification of mutations, gene expression changes and fusion transcripts by whole transcriptome RNAseq in docetaxel resistant prostate cancer cells
Ma Y; Miao Y; Peng Z; Sandgren J; De Stahl TD; Huss M; Lennartsson L; Liu Y; Nister M; Nilsson S; Li C
Journal article: SPRINGERPLUS. 2016;5(1):2084
Erratum to: Identification of mutations, gene expression changes and fusion transcripts by whole transcriptome RNAseq in docetaxel resistant prostate cancer cells.
Ma Y; Miao Y; Peng Z; Sandgren J; De Ståhl TD; Huss M; Lennartsson L; Liu Y; Nistér M; Nilsson S; Li C
Article: BIOMED RESEARCH INTERNATIONAL. 2015;2015:862039-12
Whole Exome- and mRNA-Sequencing of an AT/RT Case Reveals Few Somatic Mutations and Several Deregulated Signalling Pathways in the Context of SMARCB1 Deficiency
Sandgren J; Holm S; Marino AM; Asmundsson J; Grillner P; Nister M; de Stahl TD
Article: PLOS ONE. 2014;9(9):e108861
Human Cytomegalovirus Tegument Protein pp65 Is Detected in All Intra- and Extra-Axial Brain Tumours Independent of the Tumour Type or Grade
Libard S; Popova SN; Amini R-M; Karja V; Pietilainen T; Hamalainen KM; Sundstrom C; Hesselager G; Bergqvist M; Ekman S; Zetterling M; Smits A; Nilsson P; Pfeifer S; de Stahl TD; Enblad G; Ponten F; Alafuzoff I
Article: BRITISH JOURNAL OF CANCER. 2014;111(6):1180-1187
The prognostic value and therapeutic target role of stathmin-1 in urinary bladder cancer
Hemdan T; Linden M; Lind SB; Namuduri AV; Sjostedt E; de Stahl TD; Asplund A; Malmstrom P-U; Segersten U
Article: NATURE GENETICS. 2014;46(6):624-628
Mosaic loss of chromosome Y in peripheral blood is associated with shorter survival and higher risk of cancer
Forsberg LA; Rasi C; Malmqvist N; Davies H; Pasupulati S; Pakalapati G; Sandgren J; de Stahl TD; Zaghlool A; Giedraitis V; Lannfelt L; Score J; Cross NCP; Absher D; Janson ET; Lindgren CM; Morris AP; Ingelsson E; Lind L; Dumanski JP
Article: BMC CANCER. 2013;13:231
Age dependence of tumor genetics in unfavorable neuroblastoma: arrayCGH profiles of 34 consecutive cases, using a Swedish 25-year neuroblastoma cohort for validation
Cetinkaya C; Martinsson T; Sandgren J; Trager C; Kogner P; Dumanski J; de Stahl TD; Hedborg F
Article: JOURNAL OF NEURO-ONCOLOGY. 2012;107(1):37-49
Novel amplifications in pediatric medulloblastoma identified by genome-wide copy number profiling
Nord H; Pfeifer S; Nilsson P; Sandgren J; Popova S; Stromberg B; Alafuzoff I; Nister M; de Stahl TD
Article: GENES CHROMOSOMES & CANCER. 2011;50(2):82-94
Common pathogenetic mechanism involving human chromosome 18 in familial and sporadic ileal carcinoid tumors.
Cunningham JL; Díaz de Ståhl T; Sjöblom T; Westin G; Dumanski JP; Janson ET
Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2010;152A(10):2595-2598
Somatic mosaicism for chromosome X and Y aneuploidies in monozygotic twins heterozygous for sickle cell disease mutation.
Razzaghian HR; Shahi MH; Forsberg LA; de Ståhl TD; Absher D; Dahl N; Westerman MP; Dumanski JP
Article: ENDOCRINE-RELATED CANCER. 2010;17(3):561-579
Recurrent genomic alterations in benign and malignant pheochromocytomas and paragangliomas revealed by whole-genome array comparative genomic hybridization analysis
Sandgren J; de Stahl TD; Andersson R; Menzel U; Piotrowski A; Nord H; Backdahl M; Kiss NB; Brauckhoff M; Komorowski J; Dralle H; Hessman O; Larsson C; Akerstrom G; Bruder C; Dumanski JP; Westin G
Article: EUROPEAN JOURNAL OF HUMAN GENETICS. 2010;18(5):560-568
Frequent genetic differences between matched primary and metastatic breast cancer provide an approach to identification of biomarkers for disease progression
Poplawski AB; Jankowski M; Erickson SW; de Stahl TD; Partridge EC; Crasto C; Guo J; Gibson J; Menzel U; Bruder CEG; Kaczmarczyk A; Benetkiewicz M; Andersson R; Sandgren J; Zegarska B; Bala D; Srutek E; Allison DB; Piotrowski A; Zegarski W; Dumanski JP
Article: INTERNATIONAL JOURNAL OF CANCER. 2010;126(6):1390-1402
Focal amplifications are associated with high grade and recurrences in stage Ta bladder carcinoma
Nord H; Segersten U; Sandgren J; Wester K; Busch C; Menzel U; Komorowski J; Dumanski JP; Malmstrom P-U; de Stahl TD
Article: NEURO-ONCOLOGY. 2009;11(6):803-818
Characterization of novel and complex genomic aberrations in glioblastoma using a 32K BAC array
Nord H; Hartmann C; Andersson R; Menzel U; Pfeifer S; Piotrowski A; Bogdan A; Kloc W; Sandgren J; Olofsson T; Hesselager G; Blomquist E; Komorowski J; von Deimling A; Bruder CEG; Dumanski JP; de Stahl TD
Article: GENES CHROMOSOMES & CANCER. 2009;48(10):897-907
Genome-wide high-resolution analysis of DNA copy number alterations in NF1-associated malignant peripheral nerve sheath tumors using 32K BAC array.
Mantripragada KK; Díaz de Ståhl T; Patridge C; Menzel U; Andersson R; Chuzhanova N; Kluwe L; Guha A; Mautner V; Dumanski JP; Upadhyaya M
Article: FASEB JOURNAL. 2009;23(8):2450-2458
Enhanced susceptibility to low-dose collagen-induced arthritis in CR1/2-deficient female mice--possible role of estrogen on CR1 expression.
Nilsson KE; Andrén M; Diaz de Ståhl T; Kleinau S
Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2008;146A(23):3075-3081
Distal 22q11.2 microduplication encompassing the BCR gene.
Descartes M; Franklin J; Diaz de Ståhl T; Piotrowski A; Bruder CEG; Dumanski JP; Carroll AJ; Mikhail FM
Article: HUMAN MUTATION. 2008;29(9):1118-1124
Somatic mosaicism for copy number variation in differentiated human tissues
Piotrowski A; Bruder CEG; Andersson R; de Stahl TD; Menzel U; Sandgren J; Poplawski A; von Tell D; Crasto C; Bogdan A; Bartoszewski R; Bebok Z; Krzyzanowski M; Jankowski Z; Partridge EC; Komorowski J; Dumanski JP
Article: BIOINFORMATICS. 2008;24(6):751-758
A segmental maximum a posteriori approach to genome-wide copy number profiling
Andersson R; Bruder CEG; Piotrowski A; Menzel U; Nord H; Sandgren J; Hvidsten TR; de Stahl TD; Dumanski JP; Komorowski J
Article: HUMAN MUTATION. 2008;29(3):398-408
Profiling of copy number variations (CNVs) in healthy individuals from three ethnic groups using a human genome 32 KBAC-clone-based array
de Stahl TD; Sandgren J; Piotrowski A; Nord H; Andersson R; Menzel U; Bogdan A; Thuresson A-C; Poplawski A; von Tell D; Hansson CM; Elshafie AI; ElGhazali G; Imreh S; Nordenskjold M; Upadhyaya M; Komorowski J; Bruder CEG; Dumanski JP
Article: AMERICAN JOURNAL OF HUMAN GENETICS. 2008;82(3):763-771
Phenotypically concordant and discordant monozygotic twins display different DNA copy-number-variation profiles
Bruder CEG; Piotrowski A; Gijsbers AACJ; Andersson R; Erickson S; de Stahl TD; Menzel U; Sandgren J; von Tell D; Poplawski A; Crowley M; Crasto C; Partridge EC; Tiwari H; Allison DB; Komorowski J; van Ommen G-JB; Boomsma DI; Pedersen NL; den Dunnen JT; Wirdefeldt K; Dumanski JP
Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2007;143A(18):2178-2184
A previously unrecognized microdeletion syndrome on chromosome 22 band q11.2 encompassing the BCR gene.
Mikhail FM; Descartes M; Piotrowski A; Andersson R; Diaz de Ståhl T; Komorowski J; Bruder CEG; Dumanski JP; Carroll AJ
Article: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2007;143A(15):1760-1766
Overlapping phenotype of Wolf-Hirschhorn and Beckwith-Wiedemann syndromes in a girl with der(4)t(4;11)(pter;pter).
Mikhail FM; Sathienkijkanchai A; Robin NH; Prucka S; Biggerstaff JS; Komorowski J; Andersson R; Bruder CEG; Piotrowski A; Diaz de Ståhl T; Dumanski JP; Carroll AJ
Article: BMC GENOMICS. 2006;7:330
Array-CGH and multipoint FISH to decode complex chromosomal rearrangements
Darai-Ramqvist E; de Stahl TD; Sandlund A; Mantripragada K; Klein G; Dumanski J; Imreh S; Kost-Alimova M
Article: INTERNATIONAL JOURNAL OF ONCOLOGY. 2006;29(4):935-945
Chromosome 22 array-CGH profiling of breast cancer delimited minimal common regions of genomic imbalances and revealed frequent intra-tumoral genetic heterogeneity.
Benetkiewicz M; Piotrowski A; Díaz De Ståhl T; Jankowski M; Bala D; Hoffman J; Srutek E; Laskowski R; Zegarski W; Dumanski JP
Article: INTERNATIONAL JOURNAL OF CANCER. 2006;119(3):571-578
Identification of limited regions of genetic aberrations in patients affected with Wilms' tumor using a tiling-path chromosome 22 array.
Benetkiewicz M; Díaz de Ståhl T; Gördör A; Pfeifer S; Wittmann S; Gessler M; Dumanski JP
Article: GENOMICS. 2006;88(2):152-162
Analysis of copy number variation in the normal human population within a region containing complex segmental duplications on 22q11 using high-resolution array-CGH
de Bustos C; Diaz de Stahl T; Piotrowski A; Mantripragada KK; Buckley PG; Darai E; Hansson CM; Grigelionis G; Menzel U; Dumanski JP
Article: GENES CHROMOSOMES & CANCER. 2006;45(7):656-667
Microarray-based survey of CpG islands identifies concurrent hyper- and hypomethylation patterns in tissues derived from patients with breast cancer.
Piotrowski A; Benetkiewicz M; Menzel U; Díaz de Ståhl T; Mantripragada K; Grigelionis G; Buckley PG; Jankowski M; Hoffman J; Bała D; Srutek E; Laskowski R; Zegarski W; Dumanski JP
Article: INTERNATIONAL JOURNAL OF CANCER. 2006;118(5):1159-1164
Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH
Jarbo C; Buckley PG; Piotrowski A; Mantripragada KK; Benetkiewicz M; de Ståhl TD; Langford CF; Gregory SG; Dralle H; Gimm O; Bäckdahl M; Geli J; Larsson C; Westin G; Aring; kerström G; Dumanski JP
Article: JOURNAL OF MEDICAL GENETICS. 2006;43(1):28-38
Identification of novel deletion breakpoints bordered by segmental duplications in the NF1 locus using high resolution array-CGH.
Mantripragada KK; Thuresson A-C; Piotrowski A; Díaz de Ståhl T; Menzel U; Grigelionis G; Ferner RE; Griffiths S; Bolund L; Mautner V; Nordling M; Legius E; Vetrie D; Dahl N; Messiaen L; Upadhyaya M; Bruder CEG; Dumanski JP
Article: HUMAN MUTATION. 2005;26(6):540-549
Identification of genetic aberrations on chromosome 22 outside the NF2 locus in schwannomatosis and neurofibromatosis type 2
Buckley PG; Mantripragada KK; de Ståhl TD; Piotrowski A; Hansson CM; Kiss H; Vetrie D; Ernberg IT; Nordenskjöld M; Bolund L; Sainio M; Rouleau GA; Niimura M; Wallace AJ; Evans DGR; Grigelionis G; Menzel U; Dumanski JE
Article: HUMAN GENETICS. 2005;118(1):35-44
High-resolution array-CGH profiling of germline and tumor-specific copy number alterations on chromosome 22 in patients affected with schwannomas
de Ståhl TD; Hansson CM; de Bustos C; Mantripragada KK; Piotrowski A; Benetkiewiez M; Jarbo C; Wiklund L; Mathiesen T; Nyberg G; Collins VP; Evans DG; Ichimura K; Dumanski JP
Article: GENES CHROMOSOMES & CANCER. 2005;44(2):161-169
Chromosome 22 tiling-path array-CGH analysis identifies germ-line- and tumor-specific aberrations in patients with glioblastoma multiforme.
Díaz de Ståhl T; Hartmann C; de Bustos C; Piotrowski A; Benetkiewicz M; Mantripragada KK; Tykwinski T; von Deimling A; Dumanski JP
Article: TRENDS IN GENETICS. 2005;21(6):315-317
Copy-number polymorphisms: mining the tip of an iceberg.
Buckley PG; Mantripragada KK; Piotrowski A; Diaz de Ståhl T; Dumanski JP
Article: DRUG DISCOVERY TODAY. 2004;9(24 Suppl):S45-S52
Genomic microarrays in the spotlight.
Mantripragada KK; Buckley PG; de Ståhl TD; Dumanski JP
Article: JOURNAL OF EXPERIMENTAL MEDICINE. 2003;197(9):1183-1190
A role for complement in feedback enhancement of antibody responses by IgG3.
Díaz de Ståhl T; Dahlstrom J; Carroll MC; Heyman B
Article: HUMAN MOLECULAR GENETICS. 2002;11(25):3221-3229
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applications
Buckley PG; Mantripragada KK; Benetkiewicz M; Tapia-Páez I; de Ståhl TD; Rosenquist M; Ali H; Jarbo C; de Bustos C; Hirvelä C; Wilén BS; Fransson I; Thyr C; Johnsson BI; Bruder CEG; Menzel U; Hergersberg M; Mandahl N; Blennow E; Wedell A; Beare DM; Collins JE; Dunham I; Albertson D; Pinkel D; Bastian BC; Faruqi AF; Lasken RS; Ichimura K; Collins VP; Dumanski JP
Article: EUROPEAN JOURNAL OF IMMUNOLOGY. 2002;32(10):2915-2922
Expression of FcgammaRIII is required for development of collagen-induced arthritis.
Díaz de Ståhl T; Andrén M; Martinsson P; Verbeek JS; Kleinau S
Article: SCANDINAVIAN JOURNAL OF IMMUNOLOGY. 2001;54(5):495-500
IgG2a-mediated enhancement of antibody responses is dependent on FcRgamma+ bone marrow-derived cells.
Diaz de Ståhl T; Heyman B
Article: SCANDINAVIAN JOURNAL OF IMMUNOLOGY. 2001;53(4):381-385
IgE-mediated suppression of primary antibody responses in vivo.
Karlsson MC; Diaz de Ståhl T; Heyman B
Journal article: SCANDINAVIAN JOURNAL OF IMMUNOLOGY. 2001;53(4):331-334
No evidence for a role of FcgammaRIIB in suppression of in vivo antibody responses to erythrocytes by passively administered IgG.
Heyman B; Dahlström J; Diaz De Ståhl T; Getahun A; Wernersson S; Karlsson MC
Article: BRITISH JOURNAL OF CANCER. 1999;80(5-6):650-656
Non-autocrine, constitutive activation of Met in human anaplastic thyroid carcinoma cells in culture.
Bergström JD; Hermansson A; Diaz de Ståhl T; Heldin NE
Article: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 1999;96(5):2244-2249
Efficient IgG-mediated suppression of primary antibody responses in Fcgamma receptor-deficient mice.
Karlsson MC; Wernersson S; Diaz de Ståhl T; Gustavsson S; Heyman B
Article: BIOTECHNOLOGY LETTERS. 1995;9(7):533-538
REVERSIBLE IMMOBILIZATION OF CHEMICALLY-MODIFIED PULLULANASE
DIAZ T; STAHL U; BATISTAVIERA F; CARLSSON J
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Review: MINERVA UROLOGICA E NEFROLOGICA. 2008;60(4):205-216
Molecular genetics of bladder cancer: an update.
Díaz De Ståhl T; Segersten U; Malmström PU
Published conference paper: AMERICAN JOURNAL OF MEDICAL GENETICS PART A. 2007;143A(24):3302-3308
A patient with 22q11.2 deletion and Opitz syndrome-like phenotype has the same deletion as velocardiofacial patients.
Erickson RP; Díaz de Ståhl T; Bruder CEG; Dumanski JP
Review: TRENDS IN GENETICS. 2004;20(2):87-94
Genomic microarrays in the spotlight.
Mantripragada KK; Buckley PG; Diaz de Ståhl T; Dumanski JP
Corrigendum: JOURNAL OF EXPERIMENTAL MEDICINE. 2003;197(11):1599
A role for complement in feedback enhancement of antibody responses by IgG3 (vol 197, pg 1183, 2003)
de Stahl D; Dahlstrom J; Carroll MC; Heyman B

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Senior Forskningsspecialist, Onkologi-Patologi, Karolinska Institutet, 2022-

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Docent, Associate Professor in Medical Genetics and Genomics, Uppsala University, 2008

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