D-Index & Metrics Best Publications

Annemarie Poustka

German Cancer Research Center
Germany

Genetics

Germany

2023

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name Citations Publications World Ranking National Ranking

Genetics D-index 83 Citations 30,176 263 World Ranking 892 National Ranking 63

Research.com Recognitions

Awards & Achievements

2023 - Research.com Genetics in Germany Leader Award

Overview

What is she best known for?

The fields of study Annemarie Poustka is best known for:

Gene
Mutation
Genome

Annemarie Poustka combines Gene and Molecular biology in her studies. She conducts interdisciplinary study in the fields of Molecular biology and Genetics through her research. Her Genetics study frequently links to other fields, such as Missense mutation. She performs multidisciplinary study on Allele and Genetic linkage in her works. In her works, Annemarie Poustka conducts interdisciplinary research on Genetic linkage and Phenotype. She performs multidisciplinary studies into Phenotype and X chromosome in her work. Annemarie Poustka performs multidisciplinary study on X chromosome and Allele in her works. With her scientific publications, her incorporates both Genome and Genome project. Her study ties her expertise on Positional cloning together with the subject of Locus (genetics).

Her most cited work include:

A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets (942 citations)
Genomic rearrangement in NEMO impairs NF-κB activation and is a cause of incontinentia pigmenti (634 citations)
A Genomewide Screen for Autism: Strong Evidence for Linkage to Chromosomes 2q, 7q, and 16p (419 citations)

What are the main themes of her work throughout her whole career to date

Annemarie Poustka spends much of her time researching Genetics, Molecular biology, Cancer research, Computational biology, Pathology, Immunology, Internal medicine, Endocrinology and Cell biology. She integrates Gene with DNA in her study. Annemarie Poustka performs multidisciplinary study on DNA and Gene in her works. Annemarie Poustka performs integrative study on Chromosome and Genetic linkage. She incorporates Genome and Chromosome in her research. She conducts interdisciplinary study in the fields of Cancer and Genetics through her research.

Annemarie Poustka most often published in these fields:

Genetics (97.67%)
Gene (81.40%)
Molecular biology (37.21%)

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Variance stabilization applied to microarray data calibration and to the quantification of differential expression.

Wolfgang Huber;Anja von Heydebreck;Holger Sültmann;Annemarie Poustka.
intelligent systems in molecular biology (2002)

3062 Citations

Lambda replacement vectors carrying polylinker sequences

Anna-Maria Frischauf;Hans Lehrach;Annemarie Poustka;Noreen Murray.
Journal of Molecular Biology (1983)

2359 Citations

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts.
Nature Genetics (2007)

1546 Citations

The DNA sequence of the human X chromosome

Mark T Ross;Darren V Grafham;Alison J Coffey;Steven Scherer.
Nature (2005)

1277 Citations

Cloning of the T gene required in mesoderm formation in the mouse

Bernhard G. Herrmann;Siegfried Labeit;Annemarie Poustka;Thomas R. King.
Nature (1990)

1184 Citations

p53 gene deletion predicts for poor survival and non-response to therapy with purine analogs in chronic B-cell leukemias.

Hartmut Döhner;Konstanze Fischer;Martin Bentz;Katrin Hansen.
Blood (1995)

947 Citations

Genomic rearrangement in NEMO impairs NF-kappaB activation and is a cause of incontinentia pigmenti. The International Incontinentia Pigmenti (IP) Consortium.

Asmae Smahi;G. Courtois;P. Vabres;S. Yamaoka.
Nature (2000)

903 Citations

A full genome screen for autism with evidence for linkage to a region on chromosome 7q International Molecular Genetic Study of Autism Consortium

Anthony Bailey;Amaia Hervas;Nicola Matthews;Sarah Palferman.
Human Molecular Genetics (1998)

740 Citations

A genome-wide linkage and association scan reveals novel loci for autism

Lauren A. Weiss;Lauren A. Weiss;Dan E. Arking;Mark J. Daly;Mark J. Daly;Aravinda Chakravarti.
Nature (2009)

717 Citations

A genome-wide scan for common alleles affecting risk for autism

Richard Anney;Lambertus Klei;Dalila Pinto;Regina Regan.
Human Molecular Genetics (2010)

658 Citations

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