Achromobacter spp. genetic adaptation in cystic fibrosis

por Gabrielaite, Migle, Nielsen, Finn C., Johansen, Helle K., Marvig, Rasmus L.
Publicado 2021

Gene Loss and Acquisition in Lineages of Pseudomonas aeruginosa Evolving in Cystic Fibrosis Patient Airways

por Gabrielaite, Migle, Johansen, Helle K., Molin, Søren, Nielsen, Finn C., Marvig, Rasmus L.
Publicado 2020

Identification of 3 novel VHL germ-line mutations in Danish VHL patients

por Dandanell, Mette, Friis-Hansen, Lennart, Sunde, Lone, Nielsen, Finn C, Hansen, Thomas v O
Publicado 2012

Identification of a Danish breast/ovarian cancer family double heterozygote for BRCA1 and BRCA2 mutations

por Steffensen, Ane Y., Jønson, Lars, Ejlertsen, Bent, Gerdes, Anne-Marie, Nielsen, Finn C., Hansen, Thomas V. O.
Publicado 2010

High-density SNP arrays improve detection of HER2 amplification and polyploidy in breast tumors

por Hansen, Thomas v O, Vikesaa, Jonas, Buhl, Sine S, Rossing, Henrik H, Timmermans-Wielenga, Vera, Nielsen, Finn C
Publicado 2015

Splicing analysis of 14 BRCA1 missense variants classifies nine variants as pathogenic

por Ahlborn, Lise B., Dandanell, Mette, Steffensen, Ane Y., Jønson, Lars, Nielsen, Finn C., Hansen, Thomas v. O.
Publicado 2015

A novel DICER1 mutation identified in a female with ovarian Sertoli-Leydig cell tumor and multinodular goiter: a case report

por Rossing, Maria, Gerdes, Anne-Marie, Juul, Anders, Rechnitzer, Catherine, Rudnicki, Martin, Nielsen, Finn C, vO Hansen, Thomas
Publicado 2014

Functional characterization of BRCA1 gene variants by mini-gene splicing assay

por Steffensen, Ane Y, Dandanell, Mette, Jønson, Lars, Ejlertsen, Bent, Gerdes, Anne-Marie, Nielsen, Finn C, Hansen, Thomas vO
Publicado 2014

Transmission and Antibiotic Resistance of Achromobacter in Cystic Fibrosis

por Gabrielaite, Migle, Bartell, Jennifer A., Nørskov-Lauritsen, Niels, Pressler, Tacjana, Nielsen, Finn C., Johansen, Helle K., Marvig, Rasmus L.
Publicado 2021

Novel de novo BRCA2 mutation in a patient with a family history of breast cancer

por Hansen, Thomas V O, Bisgaard, Marie Luise, Jønson, Lars, Albrechtsen, Anders, Filtenborg-Barnkob, Bettina, Eiberg, Hans, Ejlertsen, Bent, Nielsen, Finn C
Publicado 2008

Identification of eight novel SDHB, SDHC, SDHD germline variants in Danish pheochromocytoma/paraganglioma patients

por Bennedbæk, Marc, Rossing, Maria, Rasmussen, Åse K., Gerdes, Anne-Marie, Skytte, Anne-Bine, Jensen, Uffe B., Nielsen, Finn C., Hansen, Thomas v. O.
Publicado 2016

Cancers of unknown primary origin (CUP) are characterized by chromosomal instability (CIN) compared to metastasis of know origin

por Vikeså, Jonas, Møller, Anne Kirstine H, Kaczkowski, Bogumil, Borup, Rehannah, Winther, Ole, Henao, Ricardo, Krogh, Anders, Perell, Katharina, Jensen, Flemming, Daugaard, Gedske, Nielsen, Finn C
Publicado 2015

Clusters of Conserved Beta Cell Marker Genes for Assessment of Beta Cell Phenotype

por Martens, Geert A., Jiang, Lei, Hellemans, Karine H., Stangé, Geert, Heimberg, Harry, Nielsen, Finn C., Sand, Olivier, Van Helden, Jacques, Gorus, Frans K., Pipeleers, Daniel G.
Publicado 2011

Correction: Clusters of Conserved Beta Cell Marker Genes for Assessment of Beta Cell Phenotype

por Martens, Geert A., Jiang, Lei, Hellemans, Karine H., Stangé, Geert, Heimberg, Harry, Nielsen, Finn C., Sand, Olivier, Van Helden, Jacques, Gorus, Frans K., Pipeleers, Daniel G.
Publicado 2012

Correction: Clusters of Conserved Beta Cell Marker Genes for Assessment of Beta Cell Phenotype

por Martens, Geert A., Jiang, Lei, Hellemans, Karine H., Stangé, Geert, Heimberg, Harry, Nielsen, Finn C., Sand, Olivier, Van Helden, Jacques, Gorus, Frans K., Pipeleers, Daniel G.
Publicado 2012

Correction: Clusters of Conserved Beta Cell Marker Genes for Assessment of Beta Cell Phenotype

por Martens, Geert A., Jiang, Lei, Hellemans, Karine H., Stangé, Geert, Heimberg, Harry, Nielsen, Finn C., Sand, Olivier, Van Helden, Jacques, Gorus, Frans K., Pipeleers, Daniel G.
Publicado 2012

The trans fatty acid elaidate affects the global DNA methylation profile of cultured cells and in vivo

por Flores-Sierra, José, Arredondo-Guerrero, Martín, Cervantes-Paz, Braulio, Rodríguez-Ríos, Dalia, Alvarado-Caudillo, Yolanda, Nielsen, Finn C., Wrobel, Katarzyna, Wrobel, Kazimierz, Zaina, Silvio, Lund, Gertrud
Publicado 2016

Functional examination of MLH1, MSH2, and MSH6 intronic mutations identified in Danish colorectal cancer patients

por Petersen, Sanne M, Dandanell, Mette, Rasmussen, Lene J, Gerdes, Anne-Marie, Krogh, Lotte N, Bernstein, Inge, Okkels, Henrik, Wikman, Friedrik, Nielsen, Finn C, Hansen, Thomas v O
Publicado 2013

Promoter polymorphism -119C/G in MYG1 (C12orf10) gene is related to vitiligo susceptibility and Arg4Gln affects mitochondrial entrance of Myg1

por Philips, Mari-Anne, Kingo, Külli, Karelson, Maire, Rätsep, Ranno, Aunin, Eerik, Reimann, Ene, Reemann, Paula, Porosaar, Orm, Vikeså, Jonas, Nielsen, Finn C, Vasar, Eero, Silm, Helgi, Kõks, Sulev
Publicado 2010

Application of cell-free DNA for genomic tumor profiling: a feasibility study

por Ahlborn, Lise B., Rohrberg, Kristoffer S., Gabrielaite, Migle, Tuxen, Ida V., Yde, Christina W., Spanggaard, Iben, Santoni-Rugiu, Eric, Nielsen, Finn C., Lassen, Ulrik, Mau-Sorensen, Morten, Østrup, Olga
Publicado 2019