Concepedia

Author

Bettina Lipkowitz

Max Planck Institute for Molecular Genetics

Also Known As

Bettina Lipkowitz

16

Publications

1.8K

Citations

10

H-Index

42

Concepts

All Affiliations

Max Planck Institute for Molecular GeneticsUniversity of Social Welfare and Rehabilitation SciencesHormozgan University of Medical SciencesMax Delbrück CenterShahid Beheshti University of Medical Sciences
BL

About

Bettina Lipkowitz is an author at Max Planck Institute for Molecular Genetics specializing in medicine, genetics, and neuroscience.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

7

7

1.6K

2

Natural Sciences

1

1

29

3

Public Health

1

1

79

4

Social Sciences

1

1

115

5

Biostatistics

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79

Bettina Lipkowitz

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10

Publications

1.8K

Citations

10

H-Index

YearCitations

Deep sequencing reveals 50 novel genes for recessive cognitive disorders

Hossein Najmabadi, Hao Hu, Masoud Garshasbi,

Nature

2011

975

Genetics of intellectual disability in consanguineous families

Hao Hu, Kimia Kahrizi, Luciana Musante,

Molecular Psychiatry

2018

206

Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome

Ulrike A. Nuber, Skirmantas Kriaučionis, Tim Roloff,

Human Molecular Genetics

2005

182

Gene Expression Changes in the Course of Neural Progenitor Cell Differentiation

Ulf Gurok, Christine Steinhoff, Bettina Lipkowitz,

Journal of Neuroscience

2004

115

Effect of inbreeding on intellectual disability revisited by trio sequencing

Kimia Kahrizi, Hao Hu, Masoumeh Hosseini,

Clinical Genetics

2018

79

Mutations of the aminoacyl-tRNA-synthetases SARS and WARS2 are implicated in the etiology of autosomal recessive intellectual disability

Luciana Musante, Lucia Püttmann, Kimia Kahrizi,

Human Mutation

2017

64

Different molecular mechanisms underlie placental overgrowth phenotypes caused by interspecies hybridization, cloning, and <i>Esx1</i> mutation

Umashankar Singh, Laurel E. Fohn, Teruhiko Wakayama,

Developmental Dynamics

2004

58

Two isoforms of the RAC-specific guanine nucleotide exchange factor TIAM2 act oppositely on transmission ratio distortion by the mouse t-haplotype

Yves Charron, Jürgen Willert, Bettina Lipkowitz,

PLoS Genetics

2019

29

Hybridisation-based resequencing of 17 X-linked intellectual disability genes in 135 patients reveals novel mutations in ATRX, SLC6A8 and PQBP1

Lars R. Jensen, Wei Chen, Bettina A. Moser,

European Journal of Human Genetics

2011

24

A novel <i>ALDH5A1</i> mutation is associated with succinic semialdehyde dehydrogenase deficiency and severe intellectual disability in an Iranian family

Lucia Püttmann, Henning Stehr, Masoud Garshasbi,

American Journal of Medical Genetics Part A

2013

21

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