Publications by authors named "Beata Stachowiak"

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Nipah virus infects specific subsets of porcine peripheral blood mononuclear cells.
Beata Stachowiak, Hana M Weingartl

PLoS One· June 2012

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Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q.
John B Vincent, Abdul Noor, Christian Windpassinger, Peter J Gianakopoulos, Thomas Schwarzbraun, Beata Stachowiak

Am J Med Genet B Neuropsychiatr Genet· September 2009

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Addendum. CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.
Abdul Noor, Christian Windpassinger, Megha Patel, Beata Stachowiak, Anna Mikhailov

Am J Hum Genet· November 2008

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A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints.
John B Vincent, Sanaa Choufani, Shin-ichi Horike, Beata Stachowiak, Martin Li

Psychiatr Genet· June 2008

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CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa.
Abdul Noor, Christian Windpassinger, Megha Patel, Beata Stachowiak, Anna Mikhailov

Am J Hum Genet· April 2008

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Molecular analysis of a chromosome 4 inversion segregating in a large schizophrenia kindred from Hong Kong.
Albert K Mensah, Vincenzo De Luca, Beata Stachowiak, Abdul Noor, Christian Windpassinger

Schizophr Res· September 2007

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Sequence variants within exon 1 of MECP2 occur in females with mental retardation.
Chris G Harvey, Sailesh D Menon, Beata Stachowiak, Abdul Noor, Adam Proctor

Am J Med Genet B Neuropsychiatr Genet· April 2007

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