Heidi L. Schulz

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TMEM16B, a novel protein with calcium-dependent chloride channel activity, associates with a presynaptic protein complex in photoreceptor terminals.

Heidi Stoehr, Julia B Heisig, +7 authors Heidi L. Schulz
The Journal of neuroscience : the official…
2009

Photoreceptor ribbon synapses release glutamate in response to graded changes in membrane potential evoked by vast, logarithmically scalable light intensities. Neurotransmitter release is modulated… (More)

Meta-analysis of genome scans of age-related macular degeneration.

Sheila A. Fisher, Gonçalo R. Abecasis, +22 authors Bernhard H F Weber
Human molecular genetics
2005

A genetic contribution to the development of age-related macular degeneration (AMD) is well established. Several genome-wide linkage studies have identified a number of putative susceptibility loci… (More)

The Retinome – Defining a reference transcriptome of the adult mammalian retina/retinal pigment epithelium

Heidi L. Schulz, Thomas Goetz, Juergen Kaschkoetoe, Bernhard H. F. Weber
BMC Genomics
2004

The mammalian retina is a valuable model system to study neuronal biology in health and disease. To obtain insight into intrinsic processes of the retina, great efforts are directed towards the… (More)

Characterization of three novel isoforms of the metabotrobic glutamate receptor 7 (GRM7)

Heidi L. Schulz, Heidi Stohr, Bernhard H F Weber
Neuroscience Letters
2002

The G protein-coupled metabotropic glutamate receptors (GRMs) consist of a family of eight members. Structural and functional diversity of this receptor family is achieved by the existence of… (More)

EST mining of the UniGene dataset to identify retina-specific genes.

Heidi Stoehr, Nancy Mah, Heidi L. Schulz, Andrea E. Gehrig, Susanne C Froehlich, Bernhard H F Weber
Cytogenetics and cell genetics
2000

Age-related macular degeneration (AMD) is a multifactorial disorder affecting the visual system with a high prevalence among the elderly population but with no effective therapy available at present.… (More)

Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort—Impact of Selected Deep Intronic Variants and Common SNPs

Heidi L. Schulz, Felix Grassmann, +9 authors Heidi Stoehr
Investigative ophthalmology & visual science
2017

Purpose Stargardt disease (STGD1) is an autosomal recessive retinopathy, caused by mutations in the retina-specific ATP-binding cassette transporter (ABCA4) gene. To establish the mutational spectrum… (More)

A Candidate Gene Association Study Identifies DAPL1 as a Female-Specific Susceptibility Locus for Age-Related Macular Degeneration (AMD)

Felix Grassmann, Ulrike Friedrich, +22 authors Bernhard H F Weber
NeuroMolecular Medicine
2015

Age-related macular degeneration (AMD) is the leading cause of blindness among white caucasians over the age of 50 years with a prevalence rate expected to increase markedly with an anticipated… (More)

Identification of a novel retina-specific gene located in a subtelomeric region with polymorphic distribution among multiple human chromosomes.

Nancy Mah, Heidi Stoehr, Heidi L. Schulz, Karen F. White, Bernhard H F Weber
Biochimica et biophysica acta
2001

The human retina is comprised of a large number of cell types with highly specialized functions that depend on the action of countless genes, many of which are exclusively expressed in the retina. We… (More)

Identifying differentially expressed genes in the mammalian retina and the retinal pigment epithelium by suppression subtractive hybridization.

Heidi L. Schulz, Faisal Abdel Rahman, F M Fadl El Moula, Jelena Stojic, Andrea E. Gehrig, Bernhard H F Weber
Cytogenetic and genome research
2004

Retina and retinal pigment epithelium (RPE) cells are of neuroectodermal origin with highly specialized functions in light perception. Identification and characterization of genes differentially… (More)

Genomic structure and assessment of the retinally expressed RFamide-related peptide gene in dominant cystoid macular dystrophy.

Heidi L. Schulz, Heidi Stoehr, +4 authors Bernhard H F Weber
Molecular vision
2002

PURPOSE Computer-assisted sampling of EST data contained within the UniGene human sequences collection is being used to establish a catalog of novel genes that are expressed exclusively or… (More)

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