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2010 Presidential Address: Culture: The Silent Language Geneticists Must Learn— Genetic Research with Indigenous Populations

American journal of human genetics, 2011-03, Vol.88 (3), p.254-261

McInnes, Roderick R.

2011

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Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons

Cell reports (Cambridge), 2014-06, Vol.7 (6), p.1762-1770

2014

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Neto1 is a novel CUB-domain NMDA receptor-interacting protein required for synaptic plasticity and learning

PLoS biology, 2009-02, Vol.7 (2), p.e41-e1000041

2009

Volltextzugriff (PDF)

Neto auxiliary protein interactions regulate kainate and NMDA receptor subunit localization at mossy fiber-CA3 pyramidal cell synapses

The Journal of neuroscience, 2014-01, Vol.34 (2), p.622-628

2014

Volltextzugriff (PDF)

VSX1: A gene for posterior polymorphous dystrophy and keratoconus

Human molecular genetics, 2002-05, Vol.11 (9), p.1029-1036

2002

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Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

Nature genetics, 2000-08, Vol.25 (4), p.397-401

2000

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Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene ( CRX) Essential for Maintenance of the Photoreceptor

Cell, 1997-11, Vol.91 (4), p.543-553

1997

Volltextzugriff (PDF)

Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis

Nature genetics, 2000-05, Vol.25 (1), p.67-73

2000

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A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene

American journal of human genetics, 1998-11, Vol.63 (5), p.1307-1315

1998

Volltextzugriff (PDF)

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

Nature genetics, 1996-04, Vol.12 (4), p.376-384

1996

Volltextzugriff (PDF)

A transgenic mouse line expressing cre recombinase in undifferentiated postmitotic mouse retinal bipolar cell precursors

PloS one, 2011-10, Vol.6 (10), p.e27145-e27145

2011

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The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase

Nature (London), 1992-07, Vol.358 (6383), p.239-242

1992

Volltextzugriff (PDF)

Unintentional injury during foreign travel: a review

Journal of travel medicine, 2002-11, Vol.9 (6), p.297-307

2002

Volltextzugriff (PDF)

Mutation analysis of the ROM1 gene in retinitis pigmentosa

Human molecular genetics, 1995-10, Vol.4 (10), p.1895-1902

1995

Volltextzugriff (PDF)

Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV

Proceedings of the National Academy of Sciences - PNAS, 1994-04, Vol.91 (9), p.3989-3993

1994

Volltextzugriff (PDF)

Late onset Leigh syndrome and ataxia due to a T to C mutation at bp 9,185 of mitochondrial DNA

American journal of medical genetics. Part A, 2007-04, Vol.143A (8), p.808-816

2007

Volltextzugriff (PDF)

Identical genotypes in siblings with different homocystinuric phenotypes: identification of three mutations in cystathionine β-synthase using an improved bacterial expression system

Human molecular genetics, 1994-07, Vol.3 (7), p.1103-1108

1994

Volltextzugriff (PDF)

Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome

Mammalian genome, 2000-08, Vol.11 (8), p.710-712

2000

Volltextzugriff (PDF)

Chronic illness and sexuality

Medical journal of Australia, 2003-09, Vol.179 (5), p.263-266

McInnes, Rosemary A

2003

Volltextzugriff (PDF)

Transcriptomics tool for the human Schistosoma blood flukes using microarray gene expression profiling

Experimental parasitology, 2006-11, Vol.114 (3), p.160-172

2006

Volltextzugriff (PDF)

A mutation causing DHPR deficiency results in a frameshift and a secondary splicing defect

Journal of medical genetics, 1995-03, Vol.32 (3), p.220-223

1995

Volltextzugriff (PDF)

Reducing body-like inclusions in skeletal muscle in childhood-onset acid maltase deficiency

Acta neuropathologica, 1992-12, Vol.85 (1), p.111-115

1992

Volltextzugriff (PDF)

Comparative assessment of electroglottographic and acoustic measures of jitter in pathological voices

Journal of speech, language, and hearing research, 1997-02, Vol.40 (1), p.170

1997

Volltextzugriff (PDF)

The Retinal Outer Segment Membrane Protein-1 Gene ( Rom1) Maps to the Proximal End of Mouse Chromosome 19

Genomics (San Diego, Calif.), 1994-09, Vol.23 (2), p.510-511

1994

Volltextzugriff (PDF)

Induction of fertility in a man with hypogonadotropic hypogonadism with very low seminal volume

Fertility and sterility, 1986-10, Vol.46 (4), p.730-733

1986

Volltextzugriff (PDF)

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2010 Presidential Address: Culture: The Silent Language Geneticists Must Learn— Genetic Research with Indigenous Populations

Kainate Receptors Coexist in a Functional Complex with KCC2 and Regulate Chloride Homeostasis in Hippocampal Neurons

Neto1 is a novel CUB-domain NMDA receptor-interacting protein required for synaptic plasticity and learning

Neto auxiliary protein interactions regulate kainate and NMDA receptor subunit localization at mossy fiber-CA3 pyramidal cell synapses

VSX1: A gene for posterior polymorphous dystrophy and keratoconus

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10

Cone-Rod Dystrophy Due to Mutations in a Novel Photoreceptor-Specific Homeobox Gene ( CRX) Essential for Maintenance of the Photoreceptor

Rom-1 is required for rod photoreceptor viability and the regulation of disk morphogenesis

A Range of Clinical Phenotypes Associated with Mutations in CRX, a Photoreceptor Transcription-Factor Gene

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

A transgenic mouse line expressing cre recombinase in undifferentiated postmitotic mouse retinal bipolar cell precursors

The Lowe's oculocerebrorenal syndrome gene encodes a protein highly homologous to inositol polyphosphate-5-phosphatase

Unintentional injury during foreign travel: a review

Mutation analysis of the ROM1 gene in retinitis pigmentosa

Canine X chromosome-linked hereditary nephritis: a genetic model for human X-linked hereditary nephritis resulting from a single base mutation in the gene encoding the alpha 5 chain of collagen type IV

Late onset Leigh syndrome and ataxia due to a T to C mutation at bp 9,185 of mitochondrial DNA

Identical genotypes in siblings with different homocystinuric phenotypes: identification of three mutations in cystathionine β-synthase using an improved bacterial expression system

Positioning of five genes (CASK, ARX, SAT, IMAGE cDNAs 248928 and 253949) from the human X chromosome short arm with respect to evolutionary breakpoints on the mouse X chromosome

Chronic illness and sexuality

Transcriptomics tool for the human Schistosoma blood flukes using microarray gene expression profiling

A mutation causing DHPR deficiency results in a frameshift and a secondary splicing defect

Reducing body-like inclusions in skeletal muscle in childhood-onset acid maltase deficiency

Comparative assessment of electroglottographic and acoustic measures of jitter in pathological voices

The Retinal Outer Segment Membrane Protein-1 Gene ( Rom1) Maps to the Proximal End of Mouse Chromosome 19

Induction of fertility in a man with hypogonadotropic hypogonadism with very low seminal volume

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