FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Torben Bech-Hansen

Research Profile

Disorders

Anatomy

Concepts & Ideas

Chemicals & Drugs

Physiology

Genes & Molecular Sequences

Genes

Living Beings

Mouse

Procedures

Co-author Network

Publications

TOP 3
Kyla Omilusik; John J Priatel; Rusung Tan; Hung-Sia Teh; Yiwen Teresa Wang; Douglas Waterfield; Hongjian Xu; N Torben Bech-Hansen; Xiaoxi Chen; Kyung Bok Choi; David Fedida; Rayshad Gopaul; Simon V Hunt; Adam McIntyre-Smith; Wilfred A Jefferies
The Ca(v)1.4 calcium channel is a critical regulator of T cell receptor signaling and naive T cell homeostasis.
Kevin J Cummings; Cherise Klotz; Wei-Qiao Liu; Debra E Weese-Mayer; Mary L Marazita; Margaret E Cooper; Elizabeth M Berry-Kravis; Rose Tobias; Cameron Goldie; N Torben Bech-Hansen; Richard Ja Wilson
Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP).
Samuel G Jacobson; Artur Vahe Cideciyan; Tomas S Aleman; Alexander Sumaroka; Alejandro J Roman; Leigh M Gardner; Haydn M Prosser; Monalisa Mishra; N Torben Bech-Hansen; Waldo Herrera; Sharon B Schwartz; Xue Zhong Liu; William J Kimberling; Karen P Steel; David S Williams
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Torben Bech-Hansen (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2011: Kyla Omilusik; John J Priatel; Rusung Tan; Hung-Sia Teh; Yiwen Teresa Wang; Douglas Waterfield; Hongjian Xu; N Torben Bech-Hansen; Xiaoxi Chen; Kyung Bok Choi; David Fedida; Rayshad Gopaul; Simon V Hunt; Adam McIntyre-Smith; Wilfred A Jefferies
The Ca(v)1.4 calcium channel is a critical regulator of T cell receptor signaling and naive T cell homeostasis.
Immunity 2011;35(3):349-60.
2009: Kevin J Cummings; Cherise Klotz; Wei-Qiao Liu; Debra E Weese-Mayer; Mary L Marazita; Margaret E Cooper; Elizabeth M Berry-Kravis; Rose Tobias; Cameron Goldie; N Torben Bech-Hansen; Richard Ja Wilson
Sudden infant death syndrome (SIDS) in African Americans: polymorphisms in the gene encoding the stress peptide pituitary adenylate cyclase-activating polypeptide (PACAP).
Acta paediatrica (Oslo, Norway : 1992) 2009;98(3):482-9.
2008: Samuel G Jacobson; Artur Vahe Cideciyan; Tomas S Aleman; Alexander Sumaroka; Alejandro J Roman; Leigh M Gardner; Haydn M Prosser; Monalisa Mishra; N Torben Bech-Hansen; Waldo Herrera; Sharon B Schwartz; Xue Zhong Liu; William J Kimberling; Karen P Steel; David S Williams
Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
Human molecular genetics 2008;17(15):2405-15.
2008: Noelle C Orton; A Micheil Innes; Albert E Chudley; N Torben Bech-Hansen
Unique disease heritage of the Dutch-German Mennonite population.
American journal of medical genetics. Part A 2008;146A(8):1072-87.
2008: Rajamannar Ramasubbu; Rose Tobias; N Torben Bech-Hansen
Extended evaluation of serotonin transporter gene functional polymorphisms in subjects with post-stroke depression.
Canadian journal of psychiatry. Revue canadienne de psychiatrie 2008;53(3):197-201.
2008: Mary A Raven; Noelle C Orton; Hadi Nassar; Gary A Williams; William K Stell; Gerald H Jacobs; N Torben Bech-Hansen; Benjamin E Reese
Early afferent signaling in the outer plexiform layer regulates development of horizontal cell morphology.
The Journal of comparative neurology 2008;506(5):745-58.
2007: Reetta Jalkanen; N Torben Bech-Hansen; Rose Tobias; Eeva-Marja Sankila; Maija Mäntyjärvi; Henrik Forsius; Albert de La Chapelle; Tiina Alitalo
A novel CACNA1F gene mutation causes Aland Island eye disease.
Investigative ophthalmology & visual science 2007;48(6):2498-502.
2006: Reetta Jalkanen; Maija Mäntyjärvi; Rose Tobias; Juha Isosomppi; Eeva-Marja Sankila; Tiina Alitalo; N Torben Bech-Hansen
X linked cone-rod dystrophy, CORDX3, is caused by a mutation in the CACNA1F gene.
Journal of medical genetics 2006;43(8):699-704.
2006: Rajamannar Ramasubbu; Rose Tobias; Alastair M Buchan; N Torben Bech-Hansen
Serotonin transporter gene promoter region polymorphism associated with poststroke major depression.
The Journal of neuropsychiatry and clinical neurosciences 2006;18(1):96-9.
2005: Fiona C Mansergh; Noelle C Orton; John P Vessey; Melanie R Lalonde; William K Stell; Francois Tremblay; Steven Barnes; Derrick E Rancourt; N Torben Bech-Hansen
Mutation of the calcium channel gene Cacna1f disrupts calcium signaling, synaptic transmission and cellular organization in mouse retina.
Human molecular genetics 2005;14(20):3035-46.
2005: N Torben Bech-Hansen; Josh Cockfield; Dan Liu; Cairine Logan
Isolation and characterization of the leucine-rich proteoglycan nyctalopin gene (cNyx) from chick.
Mammalian genome : official journal of the International Mammalian Genome Society 2005;16(10):815-24.
2003: Kym M Boycott; Malcolm I Parslow; Judith L Ross; Ivan P Miller; N Torben Bech-Hansen; Patrick M MacLeod
A familial contiguous gene deletion syndrome at Xp22.3 characterized by severe learning disabilities and ADHD.
American journal of medical genetics. Part A 2003;122A(2):139-47.
2001: Kym M Boycott; TA Maybaum; MJ Naylor; Richard G Weleber; J Robitaille; Y Miyake; A A Bergen; M E Pierpont; WG Pearce; N Torben Bech-Hansen
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants.
Human genetics 2001;108(2):91-7.
2000: N Torben Bech-Hansen; MJ Naylor; TA Maybaum; Rebecca Sparkes; B Koop; David G Birch; A A Bergen; Clemens F M Prinsen; R C Polomeno; A Gal; A V Drack; Maria A Musarella; Samuel G Jacobson; R S Young; Richard G Weleber
Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness.
Nature genetics 2000;26(3):319-23.
2000: Rebecca Sparkes; C G Summer; Kym M Boycott; R J Zahorchak; N Torben Bech-Hansen
Development of a 1.4-Mb BAC/PAC contig and physical map within the critical region for complete X-linked congenital stationary night blindness in Xp11.4.
Genomics 2000;68(1):97-100.
2000: MJ Naylor; Derrick E Rancourt; N Torben Bech-Hansen
Isolation and characterization of a calcium channel gene, Cacna1f, the murine orthologue of the gene for incomplete X-linked congenital stationary night blindness.
Genomics 2000;66(3):324-7.
2000: Kym M Boycott; WG Pearce; N Torben Bech-Hansen
Clinical variability among patients with incomplete X-linked congenital stationary night blindness and a founder mutation in CACNA1F.
Canadian journal of ophthalmology. Journal canadien d'ophtalmologie 2000;35(4):204-13.
1999: K L Stoddart; C Jermak; Ramaiah Nagaraja; David Schlessinger; N Torben Bech-Hansen
Physical map covering a 2 Mb region in human xp11.3 distal to DX6849.
Gene 1999;227(1):111-6.
1998: N Torben Bech-Hansen; Kym M Boycott; K J Gratton; D A Ross; L Leigh Field; WG Pearce
Localization of a gene for incomplete X-linked congenital stationary night blindness to the interval between DXS6849 and DXS8023 in Xp11.23.
Human genetics 1998;103(2):124-30.
1998: N Torben Bech-Hansen; MJ Naylor; TA Maybaum; WG Pearce; B Koop; Gerald A Fishman; M Mets; Maria A Musarella; Kym M Boycott
Loss-of-function mutations in a calcium-channel alpha1-subunit gene in Xp11.23 cause incomplete X-linked congenital stationary night blindness.
Nature genetics 1998;19(3):264-7.
1998: Kym M Boycott; WG Pearce; Maria A Musarella; Richard G Weleber; TA Maybaum; David G Birch; Y Miyake; R S Young; N Torben Bech-Hansen
Evidence for genetic heterogeneity in X-linked congenital stationary night blindness.
American journal of human genetics 1998;62(4):865-75.
1998: Kym M Boycott; R J Zahorchak; C G Summer; N P Boycott; V Kotak; C G Russell; N Torben Bech-Hansen
Construction of a 1.5-Mb bacterial artificial chromosome contig in Xp11.23, a region of high gene content.
Genomics 1998;48(3):369-72.
1997: Kym M Boycott; B J Moore; K J Gratton; K L Stoddart; Birgitte Roland; N Torben Bech-Hansen
Integration of 101 DNA markers across human Xp11 using a panel of somatic cell hybrids.
Cytogenetics and cell genetics 1997;76(3-4):223-8.
1996: Kym M Boycott; G R Halley; David Schlessinger; N Torben Bech-Hansen
A 2-megabase physical contig incorporating 43 DNA markers on the human X chromosome at p11.23-p11.22 from ZNF21 to DXS255.
Genomics 1996;33(3):488-97.
1995: N Torben Bech-Hansen; WG Pearce
X-linked retinitis pigmentosa: re-evaluation of fundus findings and the use of haplotype analysis in clarification of carrier female status.
Ophthalmic genetics 1995;16(3):113-8.
1993: N Torben Bech-Hansen; WG Pearce
Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: demonstration of homozygosity.
American journal of human genetics 1993;52(1):71-7.
1992: L Pulik; K J Gratton; N Torben Bech-Hansen
TaqI RFLP in the region of the human homeobox PBX3 gene.
Human molecular genetics 1992;1(8):656.
1992: R M Lewkonia; N Torben Bech-Hansen
Spondyloepiphyseal dysplasia tarda simulating juvenile arthritis: clinical and molecular genetic observations.
Clinical and experimental rheumatology 1992;10(4):411-4.
1992: B J Moore; S P Kwan; N Torben Bech-Hansen
A polymorphic dinucleotide repeat at the DXS7 locus.
Nucleic acids research 1992;20(4):929.
1992: N Torben Bech-Hansen; B J Moore; WG Pearce
Mapping of locus for X-linked congenital stationary night blindness (CSNB1) proximal to DXS7.
Genomics 1992;12(2):409-11.
1990: WG Pearce; N Torben Bech-Hansen
Gene locus for X-linked CSNB.
Genomics 1990;8(4):743-4.
1990: N Torben Bech-Hansen; L Leigh Field; A M Schramm; M Reedyk; IW Craig; N J Fraser; WG Pearce
A locus for X-linked congenital stationary night blindness is located on the proximal portion of the short arm of the X chromosome.
Human genetics 1990;84(5):406-8.
1989: N Torben Bech-Hansen; K J Marshall; S L Kraus
TaqI RFLP in human adenylate kinase-1 (AK1) gene region on chromosome 9.
Nucleic acids research 1989;17(10):4004.
1988: N Torben Bech-Hansen; K J Marshall; S L Kraus
Human TaqI RFLP recognized by neurofilament gene probes.
Nucleic acids research 1988;16(9):4183.