Annemarie Poustka - Concepedia

Author

Annemarie Poustka

Also Known As

A Poustka, A. Poustka, ANNEMARIE POUSTKA, Anne-Marie Poustka, AnneMarie Poustka, Annemarie Poustka, Peter Seranski, Van Engeland, H, Gerard D Schellenberg , S. M. Klauck

326

Publications

31.6K

Citations

H-Index

255

Concepts

All Affiliations

German Cancer Research Center DKFZ-ZMBH Alliance Heidelberg University Genomics (United Kingdom)Inserm

About

Annemarie Poustka is an author at German Cancer Research Center specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	62	135	15.5K
2	Natural Sciences	33	43	5.2K
3	Engineering	12	12	2.5K
4	Public Health	8	8	693
5	Health Sciences	2	2	83

Annemarie Poustka

220

Publications

27.6K

Citations

H-Index

Page 1

	Year	Citations
Variance stabilization applied to microarray data calibration and to the quantification of differential expression Wolfgang Huber, Anja von Heydebreck, Holger Sültmann, Bioinformatics	2002	2.5K
Functional impact of global rare copy number variation in autism spectrum disorders Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Nature Autism Spectrum DisordersSyndromic AutismGeneticsPsychiatric GeneticsAutism	2010	2K
Lambda replacement vectors carrying polylinker sequences Anna‐Maria Frischauf, Hans Lehrach, Annemarie Poustka, Journal of Molecular Biology Mathematical ProgrammingLambda Replacement VectorsEngineeringAlgebraic CombinatoricsComputer Science	1983	1.8K
Homozygous deletion in Wilms tumours of a zinc-finger gene identified by chromosome jumping Manfred Gessler, Annemarie Poustka, Webster K. Cavenee, Nature ChromatinGenome InstabilityDevelopmental BiologyCytogeneticsGenetic Disorder	1990	1.3K
Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters Jean Mosser, Anne‐Marie Douar, Claude‐Olivier Sarde, Nature Molecular PhysiologySignal TransductionAbc TransportersGeneticsMolecular Biology	1993	1.2K
The DNA sequence of the human X chromosome Mark T. Ross, Darren Grafham, Alison J. Coffey, Nature ChromatinDnaGeneticsChromosome BiologyMolecular Genetics	2005	1.2K
X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions Nina S. Heiss, S. W. Knight, Tom Vulliamy, Nature Genetics Genome InstabilityMendelian DisorderGenetic DisorderNatural SciencesGenetics	1998	944
Cloning of the T gene required in mesoderm formation in the mouse Bernhard G. Herrmann, Siegfried Labeit, Annemarie Poustka, Nature Developmental BiologyDevelopmental GeneticsGeneticsT GeneMorphogenesis	1990	850
A gene mutated in X–linked myotubular myopathy defines a new putative tyrosine phosphatase family conserved in yeast Jocelyn Laporte, Ling Hu, Christine Kretz, Nature Genetics Molecular PhysiologyGenetic DisorderNatural SciencesGeneticsMolecular Biology	1996	623
A genome-wide scan for common alleles affecting risk for autism Richard Anney, Lambertus Klei, Dalila Pinto, Human Molecular Genetics	2010	585

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