ASHG 2008 Annual Meeting: from enormous cohorts to individual genomes

por Feuk, Lars
Publicado 2009

Inversion variants in the human genome: role in disease and genome architecture

por Feuk, Lars
Publicado 2010

Exome RNA sequencing reveals rare and novel alternative transcripts

por Halvardson, Jonatan, Zaghlool, Ammar, Feuk, Lars
Publicado 2013

Global and unbiased detection of splice junctions from RNA-seq data

por Ameur, Adam, Wetterbom, Anna, Feuk, Lars, Gyllensten, Ulf
Publicado 2010

Transcriptome analysis of fibroblasts from schizophrenia patients reveals differential expression of schizophrenia-related genes

por Etemadikhah, Mitra, Niazi, Adnan, Wetterberg, Lennart, Feuk, Lars
Publicado 2020

Identification of novel exons and transcribed regions by chimpanzee transcriptome sequencing

por Wetterbom, Anna, Ameur, Adam, Feuk, Lars, Gyllensten, Ulf, Cavelier, Lucia
Publicado 2010

Strategies for the detection of copy number and other structural variants in the human genome

por Carson, Andrew R, Feuk, Lars, Mohammed, Mansoor, Scherer, Stephen W
Publicado 2006

Evaluation of Single-Molecule Sequencing Technologies for Structural Variant Detection in Two Swedish Human Genomes

por Fatima, Nazeefa, Petri, Anna, Gyllensten, Ulf, Feuk, Lars, Ameur, Adam
Publicado 2020

Hybrid sequencing resolves two germline ultra-complex chromosomal rearrangements consisting of 137 breakpoint junctions in a single carrier

por Eisfeldt, Jesper, Pettersson, Maria, Petri, Anna, Nilsson, Daniel, Feuk, Lars, Lindstrand, Anna
Publicado 2020

Whole genome sequencing of familial isolated oesophagus atresia uncover shared structural variants

por Klar, Joakim, Engstrand-Lilja, Helene, Maqbool, Khurram, Mattisson, Jonas, Feuk, Lars, Dahl, Niklas
Publicado 2020

Efficient cellular fractionation improves RNA sequencing analysis of mature and nascent transcripts from human tissues

por Zaghlool, Ammar, Ameur, Adam, Nyberg, Linnea, Halvardson, Jonatan, Grabherr, Manfred, Cavelier, Lucia, Feuk, Lars
Publicado 2013

Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family

por Lindholm Carlström, Eva, Halvardson, Jonatan, Etemadikhah, Mitra, Wetterberg, Lennart, Gustavson, Karl-Henrik, Feuk, Lars
Publicado 2019

Characterization of the nuclear and cytosolic transcriptomes in human brain tissue reveals new insights into the subcellular distribution of RNA transcripts

por Zaghlool, Ammar, Niazi, Adnan, Björklund, Åsa K., Westholm, Jakub Orzechowski, Ameur, Adam, Feuk, Lars
Publicado 2021

Interpretable Machine Learning Reveals Dissimilarities Between Subtypes of Autism Spectrum Disorder

por Garbulowski, Mateusz, Smolinska, Karolina, Diamanti, Klev, Pan, Gang, Maqbool, Khurram, Feuk, Lars, Komorowski, Jan
Publicado 2021

The Database of Genomic Variants: a curated collection of structural variation in the human genome

por MacDonald, Jeffrey R., Ziman, Robert, Yuen, Ryan K. C., Feuk, Lars, Scherer, Stephen W.
Publicado 2014

Copy number of pancreatic polypeptide receptor gene NPY4R correlates with body mass index and waist circumference

por Shebanits, Kateryna, Andersson-Assarsson, Johanna C., Larsson, Ingrid, Carlsson, Lena M. S., Feuk, Lars, Larhammar, Dan
Publicado 2018

Multi-Omic Investigations of a 17–19 Translocation Links MINK1 Disruption to Autism, Epilepsy and Osteoporosis

por Eisfeldt, Jesper, Schuy, Jakob, Stattin, Eva-Lena, Kvarnung, Malin, Falk, Anna, Feuk, Lars, Lindstrand, Anna
Publicado 2022

Correction: Copy number of pancreatic polypeptide receptor gene NPY4R correlates with body mass index and waist circumference

por Shebanits, Kateryna, Andersson-Assarsson, Johanna C., Larsson, Ingrid, Carlsson, Lena M. S., Feuk, Lars, Larhammar, Dan
Publicado 2022

Copy number determination of the gene for the human pancreatic polypeptide receptor NPY4R using read depth analysis and droplet digital PCR

por Shebanits, Kateryna, Günther, Torsten, Johansson, Anna C. V., Maqbool, Khurram, Feuk, Lars, Jakobsson, Mattias, Larhammar, Dan
Publicado 2019

Genome-wide sequencing for the identification of rearrangements associated with Tourette syndrome and obsessive-compulsive disorder

por Hooper, Sean D, Johansson, Anna CV, Tellgren-Roth, Christian, Stattin, Eva-Lena, Dahl, Niklas, Cavelier, Lucia, Feuk, Lars
Publicado 2012