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Simon Fisher

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Dianne F Newbury; Alessandra Renieri; Elham Sadighi Akha; Jenny C Taylor; Roberto Canitano; Simon E Fisher; Kay D Macdermot; Francesca Mari; Anthony P Monaco; Samantha J L Knight
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.
Rosie M Walker; Susan M Anderson; Pelagia Derizioti; Simon E Fisher; Gillian Hamilton; Alison E Hill; Alice C Newman; Jérôme Nicod; Fumiaki Ogawa; David J Porteous; Pippa A Thomson; Helen S Torrance; Sonja C Vernes; Kathryn L Evans
The DISC1 promoter: characterization and regulation by FOXP2.
Peter L Oliver; Henrik Oster; Stuart N Peirson; Janice W Smith; Melanie V Sobczyk; Katharina Wulff; Rachel Butler; Johanna E Chesham; Kay E Davies; Benjamin Edwards; Simon E Fisher; Sofia I H Godinho; Michael H Hastings; Sheena Lee; Achilleas Livieratos; Elizabeth S Maywood; Russell G Foster
Disrupted circadian rhythms in a mouse model of schizophrenia.

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2013: Dianne F Newbury; Alessandra Renieri; Elham Sadighi Akha; Jenny C Taylor; Roberto Canitano; Simon E Fisher; Kay D Macdermot; Francesca Mari; Anthony P Monaco; Samantha J L Knight
Dual copy number variants involving 16p11 and 6q22 in a case of childhood apraxia of speech and pervasive developmental disorder.
European journal of human genetics : EJHG 2013;21(4):361-5.
2012: Rosie M Walker; Susan M Anderson; Pelagia Derizioti; Simon E Fisher; Gillian Hamilton; Alison E Hill; Alice C Newman; Jérôme Nicod; Fumiaki Ogawa; David J Porteous; Pippa A Thomson; Helen S Torrance; Sonja C Vernes; Kathryn L Evans
The DISC1 promoter: characterization and regulation by FOXP2.
Human molecular genetics 2012;21(13):2862-72.
2012: Peter L Oliver; Henrik Oster; Stuart N Peirson; Janice W Smith; Melanie V Sobczyk; Katharina Wulff; Rachel Butler; Johanna E Chesham; Kay E Davies; Benjamin Edwards; Simon E Fisher; Sofia I H Godinho; Michael H Hastings; Sheena Lee; Achilleas Livieratos; Elizabeth S Maywood; Russell G Foster
Disrupted circadian rhythms in a mouse model of schizophrenia.
Current biology : CB 2012;22(4):314-9.
2012: Simon E Fisher; Russell G Foster; Sofia I H Godinho; Mark W Hankins; Carina A Pothecary; Stuart N Peirson
Rapid assessment of sleep-wake behavior in mice.
Journal of biological rhythms 2012;27(1):48-58.
2012: Simone Kurt; Simon E Fisher; Günter Ehret
Foxp2 mutations impair auditory-motor association learning.
PloS one 2012;7(3):e33130.
2011: Sonja C Vernes; Dilair Baban; Ariel Brewer; Jean-Baptiste Cazier; Kay E Davies; Daniel Geschwind; Matthias Groszer; Joses Ho; Helen E Lockstone; Ernesto Lowy; Cedric Mombereau; Jérôme Nicod; Peter L Oliver; Rathi Puliyadi; Jiannis Ragoussis; Natasha Sahgal; Elizabeth Spiteri; Jennifer M Taylor; Simon E Fisher
Foxp2 regulates gene networks implicated in neurite outgrowth in the developing brain.
PLoS genetics 2011;7(7):e1002145.
2011: Brian J O'Roak; Pelagia Deriziotis; Choli Lee; Laura Vives; Jerrod J Schwartz; Santhosh Girirajan; Emre Karakoc; Alexandra P Mackenzie; Sarah B Ng; Carl Baker; Mark J Rieder; Deborah A Nickerson; Raphael Bernier; Simon E Fisher; Jay Shendure; Evan E Eichler
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations.
Nature genetics 2011;43(6):585-9.
2011: Andrew J O Whitehouse; Craig E Pennell; Q W Ang; D V M Bishop; Simon E Fisher
CNTNAP2 variants affect early language development in the general population.
Genes, brain, and behavior 2011;10(4):451-6.
2010: Patrice Roll; Sonja C Vernes; Nadine Bruneau; Jennifer Cillario; Magali Ponsole-Lenfant; Annick Massacrier; Gabrielle Rudolf; Manal Khalife; Edouard Hirsch; Simon E Fisher; Pierre Szepetowski
Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.
Human molecular genetics 2010;19(24):4848-60.
2010: S Gaub; Matthias Groszer; Simon E Fisher; Günter Ehret
The structure of innate vocalizations in Foxp2-deficient mouse pups.
Genes, brain, and behavior 2010;9(4):390-401.
2010: Simon E Fisher
Genetic susceptibility to stuttering.
The New England journal of medicine 2010;362(8):750-2.
2010: Dianne F Newbury; Simon E Fisher; Anthony P Monaco
Recent advances in the genetics of language impairment.
Genome medicine 2010;2(1):6.
2009: Sonja C Vernes; Simon E Fisher
Unravelling neurogenetic networks implicated in developmental language disorders.
Biochemical Society transactions 2009;37(Pt 6):1263-9.
2009: Sonja C Vernes; Kay D MacDermot; Anthony P Monaco; Simon E Fisher
Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
European journal of human genetics : EJHG 2009;17(10):1354-8.
2009: Simone Kurt; Matthias Groszer; Simon E Fisher; Günter Ehret
Modified sound-evoked brainstem potentials in Foxp2 mutant mice.
Brain research 2009;1289():30-6.
2009: Dianne F Newbury; Laura Winchester; Laura Addis; Silvia Paracchini; Lyn-Louise Buckingham; Ann Clark; Wendy Cohen; Hilary Cowie; Katharina Dworzynski; Andrea Everitt; Ian M Goodyer; Elizabeth Hennessy; A David Kindley; Laura L Miller; Jamal Nasir; Anne O'Hare; Duncan Shaw; Zoe Simkin; Emily Simonoff; Vicky Slonims; Jocelynne Watson; Jiannis Ragoussis; Simon E Fisher; Jonathon R Seckl; Peter J Helms; Patrick F Bolton; Andrew Pickles; Gina Conti-Ramsden; Gillian Baird; Dorothy V M Bishop; Anthony P Monaco
CMIP and ATP2C2 modulate phonological short-term memory in language impairment.
American journal of human genetics 2009;85(2):264-72.
2009: Wolfgang Enard; Sabine Gehre; Kurt Hammerschmidt; Sabine M Hölter; Torsten Blass; Mehmet Somel; Martina K Brückner; Christiane Schreiweis; Christine Winter; Reinhard Sohr; Lore Becker; Victor Wiebe; Birgit Nickel; Thomas Giger; Uwe Müller; Matthias Groszer; Thure Adler; Antonio Aguilar; Ines Bolle; Julia Calzada-Wack; Claudia Dalke; Nicole Ehrhardt; Jack Favor; Helmut Fuchs; Valérie Gailus-Durner; Wolfgang Hans; Gabriele Hölzlwimmer; Anahita Javaheri; Svetoslav Kalaydjiev; Magdalena Kallnik; Eva Kling; Sandra Kunder; Ilona Mossbrugger; Beatrix Naton; Ildikó Racz; Birgit Rathkolb; Jan Rozman; Anja Schrewe; Dirk H Busch; Jochen Graw; Boris Ivandic; Martin Klingenspor; Thomas Klopstock; Markus Ollert; Leticia Quintanilla-Martinez; Holger Schulz; Eckhard Wolf; Wolfgang Wurst; Andreas Zimmer; Simon E Fisher; Rudolf Morgenstern; Thomas Arendt; Martin Hrabé de Angelis; Julia Fischer; Johannes Schwarz; Svante Pääbo
A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.
Cell 2009;137(5):961-71.
2009: Simon E Fisher; Constance Scharff
FOXP2 as a molecular window into speech and language.
Trends in genetics : TIG 2009;25(4):166-77.
2008: Sonja C Vernes; Dianne F Newbury; Brett S. Abrahams; Laura Winchester; Jérôme Nicod; Matthias Groszer; Maricela Alarcón; Peter L Oliver; Kay E Davies; Daniel Geschwind; Anthony P Monaco; Simon E Fisher
A functional genetic link between distinct developmental language disorders.
The New England journal of medicine 2008;359(22):2337-45.
2008: Milena Falcaro; Andrew Pickles; D F Newbury; L Addis; E Banfield; Simon E Fisher; Anthony P Monaco; Zoë Simkin; Gina Conti-Ramsden
Genetic and phenotypic effects of phonological short-term memory and grammatical morphology in specific language impairment.
Genes, brain, and behavior 2008;7(4):393-402.
2008: Matthias Groszer; David A Keays; Robert M J Deacon; Joseph P de Bono; Shweta Prasad-Mulcare; Simone Gaub; Muriel G Baum; Catherine A French; Jérôme Nicod; Julie A Coventry; Wolfgang Enard; Martin Fray; Steve D M Brown; Patrick M Nolan; Svante Pääbo; Keith M Channon; Rui M Costa; Jens Eilers; Günter Ehret; J Nicholas P Rawlins; Simon E Fisher
Impaired synaptic plasticity and motor learning in mice with a point mutation implicated in human speech deficits.
Current biology : CB 2008;18(5):354-62.
2007: Sonja C Vernes; Elizabeth Spiteri; Jérôme Nicod; Matthias Groszer; Jennifer M Taylor; Kay E Davies; Daniel Geschwind; Simon E Fisher
High-throughput analysis of promoter occupancy reveals direct neural targets of FOXP2, a gene mutated in speech and language disorders.
American journal of human genetics 2007;81(6):1232-50.
2007: Elizabeth Spiteri; Genevieve Konopka; Giovanni Coppola; Jamee Bomar; Michael Oldham; Jing Ou; Sonja C Vernes; Simon E Fisher; Bing Ren; Daniel Geschwind
Identification of the transcriptional targets of FOXP2, a gene linked to speech and language, in developing human brain.
American journal of human genetics 2007;81(6):1144-57.
2007: C Francks; S Maegawa; J Laurén; Brett S. Abrahams; A Velayos-Baeza; S E Medland; S Colella; M Groszer; E Z McAuley; T M Caffrey; T Timmusk; P Pruunsild; I Koppel; P A Lind; N Matsumoto-Itaba; J Nicod; L Xiong; R Joober; W Enard; B Krinsky; E Nanba; Alexandra Richardson; B P Riley; N G Martin; S M Strittmatter; Hans-Jürgen Möller; D Rujescu; D St Clair; P Muglia; J L Roos; Simon E Fisher; R Wade-Martins; G A Rouleau; John Stein; Maria Karayiorgou; Daniel Geschwind; Jiannis Ragoussis; K S Kendler; M S Airaksinen; M Oshimura; L E DeLisi; Anthony P Monaco
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia.
Molecular psychiatry 2007;12(12):1129-39, 1057.
2007: Catherine A French; Matthias Groszer; Christopher Preece; Anne-Marie Coupe; Klaus Rajewsky; Simon E Fisher
Generation of mice with a conditional Foxp2 null allele.
Genesis (New York, N.Y. : 2000) 2007;45(7):440-6.
2007: Simon E Fisher
Molecular windows into speech and language disorders.
Folia phoniatrica et logopaedica : official organ of the International Association of Logopedics and Phoniatrics (IALP) 2007;59(3):130-40.
2006: Sonja C Vernes; Jérôme Nicod; Fanny M Elahi; Julie Coventry; Niamh Kenny; Anne-Marie Coupe; Louise Bird; Kay E Davies; Simon E Fisher
Functional genetic analysis of mutations implicated in a human speech and language disorder.
Human molecular genetics 2006;15(21):3154-67.
2006: Stephanie A White; Simon E Fisher; Daniel Geschwind; Constance Scharff; Timothy E Holy
Singing mice, songbirds, and more: models for FOXP2 function and dysfunction in human speech and language.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2006;26(41):10376-9.
2006: Simon E Fisher
Tangled webs: tracing the connections between genes and cognition.
Cognition 2006;101(2):270-97.
2006: Simon E Fisher; Clyde Francks
Genes, cognition and dyslexia: learning to read the genome.
Trends in cognitive sciences 2006;10(6):250-7.
2006: Simon E Fisher; Gary F Marcus
The eloquent ape: genes, brains and the evolution of language.
Nature reviews. Genetics 2006;7(1):9-20.
2006: Matthew N Ogdie; Steven C Bakker; Simon E Fisher; Clyde Francks; May H Yang; Rita M Cantor; Sandra K Loo; Emma M van der Meulen; P Pearson; Jan K Buitelaar; Anthony P Monaco; Stanley F Nelson; Richard J Sinke; Susan L Smalley
Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13.
Molecular psychiatry 2006;11(1):5-8.
2005: Simon E Fisher
On genes, speech, and language.
The New England journal of medicine 2005;353(16):1655-7.
2005: Javier Gayán; Erik G Willcutt; Simon E Fisher; Clyde Francks; Lon R Cardon; Richard K Olson; Bruce F Pennington; Shelley D Smith; Anthony P Monaco; John C DeFries
Bivariate linkage scan for reading disability and attention-deficit/hyperactivity disorder localizes pleiotropic loci.
Journal of child psychology and psychiatry, and allied disciplines 2005;46(10):1045-56.
2005: Kay D MacDermot; Elena Bonora; Nuala Sykes; Anne-Marie Coupe; Cecilia S L Lai; Sonja C Vernes; Faraneh Vargha-Khadem; Fiona McKenzie; Robert L Smith; Anthony P Monaco; Simon E Fisher
Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
American journal of human genetics 2005;76(6):1074-80.
2004: Clyde Francks; Silvia Paracchini; Shelley D Smith; Alexandra Richardson; Thomas Scerri; Lon R Cardon; Angela J Marlow; I Laurence MacPhie; Janet Walter; Bruce F Pennington; Simon E Fisher; Richard K Olson; John C DeFries; John Stein; Anthony P Monaco
A 77-kilobase region of chromosome 6p22.2 is associated with dyslexia in families from the United Kingdom and from the United States.
American journal of human genetics 2004;75(6):1046-58.
2004: Thomas Scerri; Simon E Fisher; Clyde Francks; I Laurence MacPhie; Silvia Paracchini; Alexandra Richardson; John Stein; Anthony P Monaco
Putative functional alleles of DYX1C1 are not associated with dyslexia susceptibility in a large sample of sibling pairs from the UK.
Journal of medical genetics 2004;41(11):853-7.
2004: Matthew N Ogdie; Simon E Fisher; May Yang; Janeen Ishii; Clyde Francks; Sandra K Loo; Rita M Cantor; James T McCracken; James J McGough; Susan L Smalley; Stanley F Nelson
Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.
American journal of human genetics 2004;75(4):661-8.
2004: Sandra K Loo; Simon E Fisher; Clyde Francks; Matthew N Ogdie; I Laurence MacPhie; May Yang; James T McCracken; James J McGough; Stanley F Nelson; Anthony P Monaco; Susan L Smalley
Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects.
Molecular psychiatry 2004;9(5):485-93.
2003: Clyde Francks; Lynn E DeLisi; Sarah H Shaw; Simon E Fisher; Alexandra Richardson; John Stein; Anthony P Monaco
Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11.
Human molecular genetics 2003;12(24):3225-30.
2003: Clyde Francks; Simon E Fisher; Angela J Marlow; I Laurence MacPhie; Kathleen E Taylor; Alexandra Richardson; John Stein; Anthony P Monaco
Familial and genetic effects on motor coordination, laterality, and reading-related cognition.
The American journal of psychiatry 2003;160(11):1970-7.
2003: Cecilia S L Lai; Dianne Gerrelli; Anthony P Monaco; Simon E Fisher; Andrew J Copp
FOXP2 expression during brain development coincides with adult sites of pathology in a severe speech and language disorder.
Brain : a journal of neurology 2003;126(Pt 11):2455-62.
2003: Matthew N Ogdie; I Laurence MacPhie; Sonia L Minassian; May Yang; Simon E Fisher; Clyde Francks; Rita M Cantor; James T McCracken; James J McGough; Stanley F Nelson; Anthony P Monaco; Susan L Smalley
A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11.
American journal of human genetics 2003;72(5):1268-79.
2003: Angela J Marlow; Simon E Fisher; Clyde Francks; I Laurence MacPhie; Stacey Cherny; Alexandra Richardson; Joel B Talcott; John Stein; Anthony P Monaco; Lon R Cardon
Use of multivariate linkage analysis for dissection of a complex cognitive trait.
American journal of human genetics 2003;72(3):561-70.
2003: Clyde Francks; Lynn E DeLisi; Simon E Fisher; Steve H Laval; Judith E Rue; John Stein; Anthony P Monaco
Confirmatory evidence for linkage of relative hand skill to 2p12-q11.
American journal of human genetics 2003;72(2):499-502.
2003: Simon E Fisher; Cecilia S L Lai; Anthony P Monaco
Deciphering the genetic basis of speech and language disorders.
Annual review of neuroscience 2003;26():57-80.
2002: Simon E Fisher; John C DeFries
Developmental dyslexia: genetic dissection of a complex cognitive trait.
Nature reviews. Neuroscience 2002;3(10):767-80.
2002: Susan L Smalley; Vlad Kustanovich; Sonia L Minassian; Jennifer L Stone; Matthew N Ogdie; James J McGough; James T McCracken; I Laurence MacPhie; Clyde Francks; Simon E Fisher; Rita M Cantor; Anthony P Monaco; Stanley F Nelson
Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism.
American journal of human genetics 2002;71(4):959-63.
2002: Wolfgang Enard; Molly Przeworski; Simon E Fisher; Cecilia S L Lai; Victor Wiebe; Takashi Kitano; Anthony P Monaco; Svante Pääbo
Molecular evolution of FOXP2, a gene involved in speech and language.
Nature 2002;418(6900):869-72.
2002: Simon E Fisher; Clyde Francks; James T McCracken; James J McGough; Angela J Marlow; I Laurence MacPhie; Dianne F Newbury; Lori R Crawford; Christina G S Palmer; J Arthur Woodward; Melissa Del'Homme; Dennis P Cantwell; Stanley F Nelson; Anthony P Monaco; Susan L Smalley
A genomewide scan for loci involved in attention-deficit/hyperactivity disorder.
American journal of human genetics 2002;70(5):1183-96.
2002: Dianne F Newbury; Elena Bonora; Janine A Lamb; Simon E Fisher; Cecilia S L Lai; Gillian Baird; L Jannoun; Vicky Slonims; Carol M Stott; Melanie J Merricks; Patrick Bolton; Anthony J Bailey; Anthony P Monaco
FOXP2 is not a major susceptibility gene for autism or specific language impairment.
American journal of human genetics 2002;70(5):1318-27.
2002: Clyde Francks; Simon E Fisher; Richard K Olson; Bruce F Pennington; Shelley D Smith; John C DeFries; Anthony P Monaco
Fine mapping of the chromosome 2p12-16 dyslexia susceptibility locus: quantitative association analysis and positional candidate genes SEMA4F and OTX1.
Psychiatric genetics 2002;12(1):35-41.
2002: Clyde Francks; Simon E Fisher; I Laurence MacPhie; Alexandra Richardson; Angela J Marlow; John Stein; Anthony P Monaco
A genomewide linkage screen for relative hand skill in sibling pairs.
American journal of human genetics 2002;70(3):800-5.
2002: Simon E Fisher; Clyde Francks; Angela J Marlow; I Laurence MacPhie; Dianne F Newbury; Lon R Cardon; Yumiko Ishikawa-Brush; Alexandra Richardson; Joel B Talcott; Javier Gayán; Richard K Olson; Bruce F Pennington; Shelley D Smith; John C DeFries; John Stein; Anthony P Monaco
Independent genome-wide scans identify a chromosome 18 quantitative-trait locus influencing dyslexia.
Nature genetics 2002;30(1):86-91.
2001: Cecilia S L Lai; Simon E Fisher; J A Hurst; Faraneh Vargha-Khadem; Anthony P Monaco
A forkhead-domain gene is mutated in a severe speech and language disorder.
Nature 2001;413(6855):519-23.
2001: M Ruby Siddiqui; Sarah Meisner; Kerrie Tosh; K Balakrishnan; Satish Ghei; Simon E Fisher; M Golding; N P Shanker Narayan; T Sitaraman; U Sengupta; Ramasamy Pitchappan; Adrian V S Hill
A major susceptibility locus for leprosy in India maps to chromosome 10p13.
Nature genetics 2001;27(4):439-41.
2001: Angela J Marlow; Simon E Fisher; Alexandra Richardson; Clyde Francks; Joel B Talcott; Anthony P Monaco; John Stein; Lon R Cardon
Investigation of quantitative measures related to reading disability in a large sample of sib-pairs from the UK.
Behavior genetics 2001;31(2):219-30.
2000: Cecilia S L Lai; Simon E Fisher; J A Hurst; ER Levy; S Hodgson; M Fox; Steve Jeremiah; Sue Povey; D C Jamison; Eric Green; Faraneh Vargha-Khadem; Anthony P Monaco
The SPCH1 region on human 7q31: genomic characterization of the critical interval and localization of translocations associated with speech and language disorder.
American journal of human genetics 2000;67(2):357-68.
2000: Clyde Francks; Simon E Fisher; Angela J Marlow; Alexandra Richardson; John Stein; Anthony P Monaco
A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability.
Prostaglandins, leukotrienes, and essential fatty acids 2000;63(1-2):27-31.
1999: K Tanaka; Simon E Fisher; IW Craig
Characterization of novel promoter and enhancer elements of the mouse homologue of the Dent disease gene, CLCN5, implicated in X-linked hereditary nephrolithiasis.
Genomics 1999;58(3):281-92.
1999: Simon E Fisher; John Stein; Anthony P Monaco
A genome-wide search strategy for identifying quantitative trait loci involved in reading and spelling disability (developmental dyslexia).
European child & adolescent psychiatry 1999;8 Suppl 3():47-51.
1999: Simon E Fisher; Angela J Marlow; J Lamb; Elena Maestrini; D F Williams; Alexandra Richardson; Daniel E Weeks; John Stein; Anthony P Monaco
A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.
American journal of human genetics 1999;64(1):146-56.
1998: Simon E Fisher; Faraneh Vargha-Khadem; Kate E Watkins; Anthony P Monaco; Marcus E Pembrey
Localisation of a gene implicated in a severe speech and language disorder.
Nature genetics 1998;18(2):168-70.
1997: Simon E Fisher; Alfredo Ciccodicola; K Tanaka; Anna Curci; S Desicato; Michele D'Urso; IW Craig
Sequence-based exon prediction around the synaptophysin locus reveals a gene-rich area containing novel genes in human proximal Xp.
Genomics 1997;45(2):340-7.
1997: SE Lloyd; W Gunther; SH Pearce; A Thomson; Maria Luisa BIANCHI; M Bosio; I W Craig; Simon E Fisher; Steven J Scheinman; Oliver Wrong; TJ Jentsch; Rajesh V Thakker
Characterisation of renal chloride channel, CLCN5, mutations in hypercalciuric nephrolithiasis (kidney stones) disorders.
Human molecular genetics 1997;6(8):1233-9.
1996: SE Lloyd; SH Pearce; Simon E Fisher; Klaus Steinmeyer; B Schwappach; Steven J Scheinman; Brian Harding; Alessandra Bolino; M Devoto; Paul Goodyer; S P Rigden; Oliver Wrong; Thomas J Jentsch; IW Craig; Rajesh V Thakker
A common molecular basis for three inherited kidney stone diseases.
Nature 1996;379(6564):445-9.
1996: M A Weterman; M Wilbrink; I Janssen; H A Janssen; Eva van den Berg; Simon E Fisher; I Craig; Ad Geurts van Kessel
Molecular cloning of the papillary renal cell carcinoma-associated translocation (X;1)(p11;q21) breakpoint.
Cytogenetics and cell genetics 1996;75(1):2-6.
1995: Simon E Fisher; I van Bakel; SE Lloyd; SH Pearce; Rajesh V Thakker; IW Craig
Cloning and characterization of CLCN5, the human kidney chloride channel gene implicated in Dent disease (an X-linked hereditary nephrolithiasis).
Genomics 1995;29(3):598-606.
1995: Simon E Fisher; E Hatchwell; A Chand; N Ockenden; Anthony P Monaco; IW Craig
Construction of two YAC contigs in human Xp11.23-p11.22, one encompassing the loci OATL1, GATA, TFE3, and SYP, the other linking DXS255 to DXS146.
Genomics 1995;29(2):496-502.
1995: HJ Blair; M Ho; Anthony P Monaco; Simon E Fisher; IW Craig; Y Boyd
High-resolution comparative mapping of the proximal region of the mouse X chromosome.
Genomics 1995;28(2):305-10.
1994: Simon E Fisher; Graeme C M Black; SE Lloyd; E Hatchwell; Oliver Wrong; Rajesh V Thakker; IW Craig
Isolation and partial characterization of a chloride channel gene which is expressed in kidney and is a candidate for Dent's disease (an X-linked hereditary nephrolithiasis).
Human molecular genetics 1994;3(11):2053-9.