Lars Feuk

Lars Feuk

Uppsala Universitet

H-index: 53

Europe-Sweden

About Lars Feuk

Lars Feuk, With an exceptional h-index of 53 and a recent h-index of 34 (since 2020), a distinguished researcher at Uppsala Universitet, specializes in the field of Human Genomics.

His recent articles reflect a diverse array of research interests and contributions to the field:

Long-read sequencing and optical mapping generates near T2T assemblies that resolves a centromeric translocation

Towards routine long-read sequencing for rare disease: a national pilot study on chromosomal rearrangements

Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH

Long-read whole-genome analysis of human single cells

PB1709: A COMPLETE DIGITAL KARYOTYPE OF THE B-CELL LEUKEMIA REH CELL LINE RESOLVED BY LONG-READ SEQUENCING

A complete digital karyotype of the B-cell leukemia REH cell line resolved by long-read sequencing

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

CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations

Lars Feuk Information

University

Uppsala Universitet

Position

Professor

Citations(all)

34837

Citations(since 2020)

7976

Cited By

29969

hIndex(all)

53

hIndex(since 2020)

34

i10Index(all)

88

i10Index(since 2020)

73

Email

University Profile Page

Uppsala Universitet

Lars Feuk Skills & Research Interests

Human Genomics

Top articles of Lars Feuk

Title

Journal

Author(s)

Publication Date

Long-read sequencing and optical mapping generates near T2T assemblies that resolves a centromeric translocation

Scientific Reports

Esmee ten Berk de Boer

Adam Ameur

Ignas Bunikis

Marlene Ek

Eva-Lena Stattin

...

2024/4/18

Towards routine long-read sequencing for rare disease: a national pilot study on chromosomal rearrangements

medRxiv

Jesper Eisfeldt

Adam Ameur

Felix Lenner

Esmee Ten Berk de Boer

Marlene Ek

...

2023/12/17

Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH

BMC Research Notes

Mariya Lysenkova Wiklander

Elin Övernäs

Johanna Lagensjö

Amanda Raine

Anna Petri

...

2023/10/10

Long-read whole-genome analysis of human single cells

Nature Communications

Joanna Hård

Jeff E Mold

Jesper Eisfeldt

Christian Tellgren-Roth

Susana Häggqvist

...

2023/8/24

PB1709: A COMPLETE DIGITAL KARYOTYPE OF THE B-CELL LEUKEMIA REH CELL LINE RESOLVED BY LONG-READ SEQUENCING

HemaSphere

Mariya Lysenkova Wiklander

Gustav Arvidsson

Ignas Bunikis

Anders Lundmark

Amanda Raine

...

2023/8/1

A complete digital karyotype of the B-cell leukemia REH cell line resolved by long-read sequencing

bioRxiv

Mariya Lysenkova Wiklander

Gustav Arvidsson

Ignas Bunikis

Anders Lundmark

Amanda Raine

...

2023/3/10

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

International Journal of Molecular Sciences

Jesper Eisfeldt

Jakob Schuy

Eva-Lena Stattin

Malin Kvarnung

Anna Falk

...

2022/8/20

CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations

Nature Communications

Ida Höijer

Anastasia Emmanouilidou

Rebecka Östlund

Robin Van Schendel

Selma Bozorgpana

...

2022/2/2

Interpretable machine learning reveals dissimilarities between subtypes of autism spectrum disorder

Frontiers in genetics

Mateusz Garbulowski

Karolina Smolinska

Klev Diamanti

Gang Pan

Khurram Maqbool

...

2021/2/25

R. ROSETTA: an interpretable machine learning framework

BMC Bioinformatics

Mateusz Garbulowski

Klev Diamanti

Karolina Smolińska

Nicholas Baltzer

Patricia Stoll

...

2021/12

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

Scientific reports

Ammar Zaghlool

Adnan Niazi

Åsa K Björklund

Jakub Orzechowski Westholm

Adam Ameur

...

2021/2/18

Transcriptome analysis of post-mortem brain tissue reveals up-regulation of the complement cascade in a subgroup of schizophrenia patients

Genes

Eva Lindholm Carlström

Adnan Niazi

Mitra Etemadikhah

Jonatan Halvardson

Stefan Enroth

...

2021/8/13

Proteomic alterations in a subgroup of schizophrenia patients using postmortem brain tissue

Mitra Etemadikhah

Nima Rafati

Hongxing Zhao

Lars Feuk

2021

DLG4-related synaptopathy: a new rare brain disorder

Genetics in Medicine

Agustí Rodríguez-Palmero

Melissa Maria Boerrigter

David Gómez-Andrés

Kimberly A Aldinger

Íñigo Marcos-Alcalde

...

2021/5

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

Human genetics

Jesper Eisfeldt

Maria Pettersson

Anna Petri

Daniel Nilsson

Lars Feuk

...

2021/5

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

Scientific Reports

Mitra Etemadikhah

Adnan Niazi

Lennart Wetterberg

Lars Feuk

2020/1/20

Amplification-free long-read sequencing reveals unforeseen CRISPR-Cas9 off-target activity

Genome biology

Ida Höijer

Josefin Johansson

Sanna Gudmundsson

Chen-Shan Chin

Ignas Bunikis

...

2020/12

Evaluation of single-molecule sequencing technologies for structural variant detection in two swedish human genomes

Genes

Nazeefa Fatima

Anna Petri

Ulf Gyllensten

Lars Feuk

Adam Ameur

2020/11/30

Exploring autoantibody signatures in brain tissue from patients with severe mental illness

Translational psychiatry

David Just

Anna Månberg

Nicholas Mitsios

Craig A Stockmeier

Grazyna Rajkowska

...

2020/11/18

Identification and rescue of a tRNA wobble inosine deficiency causing intellectual disability disorder

Rna

Jillian Ramos

Melissa Proven

Jonatan Halvardson

Felix Hagelskamp

Ekaterina Kuchinskaya

...

2020/11/1

See List of Professors in Lars Feuk University(Uppsala Universitet)

Lars Feuk FAQs

What is Lars Feuk's h-index at Uppsala Universitet?

The h-index of Lars Feuk has been 34 since 2020 and 53 in total.

What are Lars Feuk's top articles?

The articles with the titles of

Long-read sequencing and optical mapping generates near T2T assemblies that resolves a centromeric translocation

Towards routine long-read sequencing for rare disease: a national pilot study on chromosomal rearrangements

Genomic, transcriptomic and epigenomic sequencing data of the B-cell leukemia cell line REH

Long-read whole-genome analysis of human single cells

PB1709: A COMPLETE DIGITAL KARYOTYPE OF THE B-CELL LEUKEMIA REH CELL LINE RESOLVED BY LONG-READ SEQUENCING

A complete digital karyotype of the B-cell leukemia REH cell line resolved by long-read sequencing

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

CRISPR-Cas9 induces large structural variants at on-target and off-target sites in vivo that segregate across generations

...

are the top articles of Lars Feuk at Uppsala Universitet.

What are Lars Feuk's research interests?

The research interests of Lars Feuk are: Human Genomics

What is Lars Feuk's total number of citations?

Lars Feuk has 34,837 citations in total.