Morten Krogh Herlin

Aarhus University

Denmark

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Articles (19)

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2025

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2021

Collaborators (21)

Signe Beck-Nielsen

Aarhus University

DENMARK

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Stina Lou

Aarhus University

DENMARK

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Sigrun Schmidt

Aarhus University

DENMARK

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Per Höllsberg

DENMARK

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Vivien Schack

Aarhus University

DENMARK

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Rasmus Kjeldsen Jensen

Aarhus University

DENMARK

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Uffe Birk Jensen

Aarhus University

DENMARK

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Pauline Dupaigne

FRANCE

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Gregers Rom Andersen

Aarhus University

DENMARK

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Francesco Benedicenti

ITALY

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Ida Vogel

Aarhus University

DENMARK

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Pernille J. Vinholt

Odense University Hospital

DENMARK

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Hans‐Christian Beck

DENMARK

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Jens Magnus Bernth Jensen

Aarhus University

DENMARK

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Coralie Fouquet

CNRS

FRANCE

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Mathias Rathe

DENMARK

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Laura Krogh Herlin

Aarhus University

DENMARK

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Jan Komorowski

Senior Professor of Bioinformatics

Uppsala University

SWEDEN

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Linda Holmfeldt

Uppsala University Hospital

SWEDEN

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Mattias Vesterlund

Karolinska Institutet

SWEDEN

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Guillaume CHEVREUX

Head of Proteomics Core Facility

Institut Jacques Monod

FRANCE

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Morten Krogh Herlin

Research Interests

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Articles (19)

Characteristics and prognosis of paediatric normal karyotype acute myeloid leukaemia

Life Beyond Childhood: Insight Into the Lived Experience of 91 Adults With KBG Syndrome Through an Online Patient/Caregiver‐Reported Co‐Produced Questionnaire

Understanding the diagnostic odyssey of women with Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome in Denmark

Experiences of vaginal lengthening treatment and sexual well‐being in women with Mayer–Rokitansky–Küster–Hauser (MRKH) syndrome: An interview study

Phenotypes, Genetics, and Estimated Prevalence of Focal Dermal Hypoplasia (Goltz Syndrome): A Single‐Center Report

Natural history of adults with KBG syndrome

Clinical presentation and genetics of tricho-rhino-phalangeal syndrome (TRPS) type 1

Genetics of Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome

Monozygotic triplets with juvenile-onset autoimmunity and 18p microdeletion involving PTPRM

Proteogenomic analysis of acute myeloid leukemia associates relapsed disease with reprogrammed energy metabolism both in adults and children

A life course perspective on Mayer-Rokitansky-Küster-Hauser syndrome: women’s experiences and negotiations of living with an underdeveloped uterus and vagina

Description of a novel subtype of acute myeloid leukemia defined by recurrent CBFB insertions

Congenital mirror movements are associated with defective polymerisation of RAD51

Compromised PAR1 Activation—A Cause for Bleeding in XMEN?

Novel homozygous CD46 variant with C-isoform expression affects C3b inactivation in atypical hemolytic uremic syndrome

Transcriptomic analysis reveals proinflammatory signatures associated with acute myeloid leukemia progression.

Autosomal dominant sleep-related hypermotor epilepsy caused by a previously unreported CHRNA4 variant

What Is Abnormal in Normal Karyotype Acute Myeloid Leukemia in Children? Analysis of the Mutational Landscape and Prognosis of the TARGET-AML Cohort

Genomic characterization of relapsed acute myeloid leukemia reveals novel putative therapeutic targets.

Collaborators (21)

Signe Beck-Nielsen

Stina Lou

Sigrun Schmidt

Per Höllsberg

Vivien Schack

Rasmus Kjeldsen Jensen

Uffe Birk Jensen

Pauline Dupaigne

Gregers Rom Andersen

Francesco Benedicenti

Ida Vogel

Pernille J. Vinholt

Hans‐Christian Beck

Jens Magnus Bernth Jensen

Coralie Fouquet

Mathias Rathe

Laura Krogh Herlin

Jan Komorowski

Linda Holmfeldt

Mattias Vesterlund

Guillaume CHEVREUX

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