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Lars Riff Jensen | Researchclopedia

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Lars Riff Jensen

Universitätsmedizin Greifswald

22

Works

2,277

Citations

16

h-index

16

i10-index

Research Topics

Genetics and Neurodevelopmental Disorders Chronic Myeloid Leukemia Treatments Epigenetics and DNA Methylation

Affiliations

Max Planck Society2002–2011

Universitätsmedizin Greifswald2013–2026

Max Planck Institute for Molecular Genetics2002–2011

Charité - Universitätsmedizin Berlin2007–2007

Top Works

Duplication of the MECP2 Region Is a Frequent Cause of Severe Mental Retardation and Progressive Neurological Symptoms in Males

Hilde Van Esch,Marijke Bauters,et al.

2005625 citations

Microtubule and mitosis dynamics

Metabolism and Genetic Disorders

Mutations in the JARID1C Gene, Which Is Involved in Transcriptional Regulation and Chromatin Remodeling, Cause X-Linked Mental Retardation

Lars Riff Jensen,M Amende,et al.

2005374 citations

A novel X-linked recessive mental retardation syndrome comprising macrocephaly and ciliary dysfunction is allelic to oral–facial–digital type I syndrome

Bartłomiej Budny,Wei Chen,et al.

2006189 citations

Mutations in the polyglutamine binding protein 1 gene cause X-linked mental retardation

Vera M. Kalscheuer,Kristine Freude,et al.

2003168 citations

A Defect in the Ionotropic Glutamate Receptor 6 Gene (GRIK2) Is Associated with Autosomal Recessive Mental Retardation

Mohammad Mahdi Motazacker,Benjamin R. Rost,et al.

2007158 citations

Similar Splice-Site Mutations of the ATP7A Gene Lead to Different Phenotypes: Classical Menkes Disease or Occipital Horn Syndrome

Lisbeth Birk Møller,Zeynep Tümer,et al.

2000127 citations

NovelJARID1C/SMCX mutations in patients with X-linked mental retardation

Andreas Tzschach,Steffen Lenzner,et al.

2006125 citations

Mutation frequencies of X-linked mental retardation genes in families from the EuroMRX consortium

Arjan P.M. de Brouwer,Helger G. Yntema,et al.

2007121 citations

Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci

Hossein Najmabadi,Mohammad Mahdi Motazacker,et al.

2006103 citations