2023 - Research.com Genetics in Germany Leader Award
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).
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.
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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)
Lambda replacement vectors carrying polylinker sequences
Anna-Maria Frischauf;Hans Lehrach;Annemarie Poustka;Noreen Murray.
Journal of Molecular Biology (1983)
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts.
Nature Genetics (2007)
The DNA sequence of the human X chromosome
Mark T Ross;Darren V Grafham;Alison J Coffey;Steven Scherer.
Cloning of the T gene required in mesoderm formation in the mouse
Bernhard G. Herrmann;Siegfried Labeit;Annemarie Poustka;Thomas R. King.
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.
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.
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)
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.
A genome-wide scan for common alleles affecting risk for autism
Richard Anney;Lambertus Klei;Dalila Pinto;Regina Regan.
Human Molecular Genetics (2010)
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