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David Callen

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Neilsen Paul M; Cheney Kelly M; Li Chia-Wei; Chen J Don; Cawrse Jacqueline E; Schulz Renée B; Powell Jason A; Kumar Raman; Callen David F
Identification of ANKRD11 as a p53 coactivator.
Kumar Raman; Cheney Kelly M; McKirdy Ross; Neilsen Paul M; Schulz Renèe B; Lee Jaclyn; Cohen Juliane; Booker Grant W; Callen David F
CBFA2T3-ZNF652 corepressor complex regulates transcription of the E-box gene HEB.
Kumar Raman; Manning Jantina; Spendlove Hayley E; Kremmidiotis Gabriel; McKirdy Ross; Lee Jaclyn; Millband David N; Cheney Kelly M; Stampfer Martha R; Dwivedi Prem P; Morris Howard A; Callen David F
ZNF652, a novel zinc finger protein, interacts with the putative breast tumor suppressor CBFA2T3 to repress transcription.

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All Publications

2008: Neilsen Paul M; Cheney Kelly M; Li Chia-Wei; Chen J Don; Cawrse Jacqueline E; Schulz Renée B; Powell Jason A; Kumar Raman; Callen David F
Identification of ANKRD11 as a p53 coactivator.
Journal of cell science 2008;121(Pt 21):3541-52.
2008: Kumar Raman; Cheney Kelly M; McKirdy Ross; Neilsen Paul M; Schulz Renèe B; Lee Jaclyn; Cohen Juliane; Booker Grant W; Callen David F
CBFA2T3-ZNF652 corepressor complex regulates transcription of the E-box gene HEB.
The Journal of biological chemistry 2008;283(27):19026-38.
2006: Kumar Raman; Manning Jantina; Spendlove Hayley E; Kremmidiotis Gabriel; McKirdy Ross; Lee Jaclyn; Millband David N; Cheney Kelly M; Stampfer Martha R; Dwivedi Prem P; Morris Howard A; Callen David F
ZNF652, a novel zinc finger protein, interacts with the putative breast tumor suppressor CBFA2T3 to repress transcription.
Molecular cancer research : MCR 2006;4(9):655-65.
2005: Kumar Raman; Neilsen Paul M; Crawford Joanne; McKirdy Ross; Lee Jaclyn; Powell Jason A; Saif Zarqa; Martin Julie M; Lombaerts Marc; Cornelisse Cees J; Cleton-Jansen Anne-Marie; Callen David F
FBXO31 is the chromosome 16q24.3 senescence gene, a candidate breast tumor suppressor, and a component of an SCF complex.
Cancer research 2005;65(24):11304-13.
2004: Bais Anthony J; Gardner Alison E; McKenzie Olivia L D; Callen David F; Sutherland Grant R; Kremmidiotis Gabriel
Aberrant CBFA2T3B gene promoter methylation in breast tumors.
Molecular cancer 2004;3():22.
2004: Lower K M; Kumar R; Woollatt E; Villard L; Gecz J; Sutherland G R; Callen D F
Partial androgen insensitivity syndrome and t(X;5): are there upstream regulatory elements of the androgen receptor gene?
Hormone research 2004;62(4):208-14.
2004: Bhalla Kavita; Phillips Hilary A; Crawford Joanna; McKenzie Olivia L D; Mulley John C; Eyre Helen; Gardner Alison E; Kremmidiotis Gabriel; Callen David F
The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.
Journal of human genetics 2004;49(6):308-11.
2003: Daniel Art; Baker Elizabeth; Chia Nicole; Haan Eric; Malafiej Paul; Hinton Lyn; Clarke Nigel; Adès Lesley; Darmanian Artur; Callen David
Recombinants of intrachromosomal transposition of subtelomeres in chromosomes 1 and 2: a cause of minute terminal chromosomal imbalances.
American journal of medical genetics. Part A 2003;117A(1):57-64.
2003: Cavanaugh J A; Adams K E; Quak E J; Bryce M E; O'Callaghan N J; Rodgers H J; Magarry G R; Butler W J; Eaden J A; Roberts-Thomson I C; Pavli P; Wilson S R; Callen D F
CARD15/NOD2 risk alleles in the development of Crohn's disease in the Australian population.
Annals of human genetics 2003;67(Pt 1):35-41.
2002: Callen D F; Eyre H; McDonnell S; Schuffenhauer S; Bhalla K
A complex rearrangement involving simultaneous translocation and inversion is associated with a change in chromatin compaction.
Chromosoma 2002;111(3):170-5.
2002: Powell Jason A; Gardner Alison E; Bais Anthony J; Hinze Susan J; Baker Elizabeth; Whitmore Scott; Crawford Joanna; Kochetkova Marina; Spendlove Hayley E; Doggett Norman A; Sutherland Grant R; Callen David F; Kremmidiotis Gabriel
Sequencing, transcript identification, and quantitative gene expression profiling in the breast cancer loss of heterozygosity region 16q24.3 reveal three potential tumor-suppressor genes.
Genomics 2002;80(3):303-10.
2002: Kochetkova Marina; McKenzie Olivia L D; Bais Anthony J; Martin Julie M; Secker Genevieve A; Seshadri Ram; Powell Jason A; Hinze Susan J; Gardner Alison E; Spendlove Hayley E; O'Callaghan Nathan J; Cleton-Jansen Anne-Marie; Cornelisse Cees; Whitmore Scott A; Crawford Joanna; Kremmidiotis Gabriel; Sutherland Grant R; Callen David F
CBFA2T3 (MTG16) is a putative breast tumor suppressor gene from the breast cancer loss of heterozygosity region at 16q24.3.
Cancer research 2002;62(16):4599-604.
2002: Baker E; Hinton L; Callen D F; Haan E A; Dobbie A; Sutherland G R
A familial cryptic subtelomeric deletion 12p with variable phenotypic effect.
Clinical genetics 2002;61(3):198-201.
2002: Callen David F; Crawford Joanne; Derwas Cathy; Cleton-Jansen Anne-Marie; Cornelisse Cees J; Baker Elizabeth
Defining regions of loss of heterozygosity of 16q in breast cancer cell lines.
Cancer genetics and cytogenetics 2002;133(1):76-82.
2002: Baker Elizabeth; Hinton Lyn; Callen David F; Altree Meryl; Dobbie Angus; Eyre Helen J; Sutherland Grant R; Thompson Elizabeth; Thompson Peter; Woollatt Erica; Haan Eric
Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies.
American journal of medical genetics 2002;107(4):285-93.
2001: Cai L; Lumsden A; Guenther U P; Neldner S A; Zäch S; Knoblauch H; Ramesar R; Hohl D; Callen D F; Neldner K H; Lindpaintner K; Richards R I; Struk B
A novel Q378X mutation exists in the transmembrane transporter protein ABCC6 and its pseudogene: implications for mutation analysis in pseudoxanthoma elasticum.
Journal of molecular medicine (Berlin, Germany) 2001;79(9):536-46.
2001: Kremmidiotis G; Gardner A E; Settasatian C; Savoia A; Sutherland G R; Callen D F
Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein.
Genomics 2001;76(1-3):58-65.
2001: Ryall R G; Callen D; Cocciolone R; Duvnjak A; Esca R; Frantzis N; Gjerde E M; Haan E A; Hocking T; Sutherland G; Thomas D W; Webb F
Karyotypes found in the population declared at increased risk of Down syndrome following maternal serum screening.
Prenatal diagnosis 2001;21(7):553-7.
2001: Cleton-Jansen A M; Callen D F; Seshadri R; Goldup S; Mccallum B; Crawford J; Powell J A; Settasatian C; van Beerendonk H; Moerland E W; Smit V T; Harris W H; Millis R; Morgan N V; Barnes D; Mathew C G; Cornelisse C J
Loss of heterozygosity mapping at chromosome arm 16q in 712 breast tumors reveals factors that influence delineation of candidate regions.
Cancer research 2001;61(3):1171-7.
1999: Callen D F; Eyre H; Fang Y Y; Guan X Y; Veleba A; Martin N J; McGill J; Haan E A
Origins of accessory small ring marker chromosomes derived from chromosome 1.
Journal of medical genetics 1999;36(11):847-53.
1999: Savino M; d'Apolito M; Centra M; van Beerendonk H M; Cleton-Jansen A M; Whitmore S A; Crawford J; Callen D F; Zelante L; Savoia A
Characterization of copine VII, a new member of the copine family, and its exclusion as a candidate in sporadic breast cancers with loss of heterozygosity at 16q24.3.
Genomics 1999;61(2):219-26.
1999: Settasatian C; Whitmore S A; Crawford J; Bilton R L; Cleton-Jansen A M; Sutherland G R; Callen D F
Genomic structure and expression analysis of the spastic paraplegia gene, SPG7.
Human genetics 1999;105(1-2):139-44.
1999: Cleton-Jansen A M; Moerland E W; Pronk J C; van Berkel C G; Apostolou S; Crawford J; Savoia A; Auerbach A D; Mathew C G; Callen D F; Cornelisse C J
Mutation analysis of the Fanconi anaemia A gene in breast tumours with loss of heterozygosity at 16q24.3.
British journal of cancer 1999;79(7-8):1049-52.
1999: Kremmidiotis G; Lensink I L; Bilton R L; Woollatt E; Chataway T K; Sutherland G R; Callen D F
The Batten disease gene product (CLN3p) is a Golgi integral membrane protein.
Human molecular genetics 1999;8(3):523-31.
1999: Crawford J; Ianzano L; Savino M; Whitmore S; Cleton-Jansen A M; Settasatian C; d'apolito M; Seshadri R; Pronk J C; Auerbach A D; Verlander P C; Mathew C G; Tipping A J; Doggett N A; Zelante L; Callen D F; Savoia A
The PISSLRE gene: structure, exon skipping, and exclusion as tumor suppressor in breast cancer.
Genomics 1999;56(1):90-7.
1999: Bhalla K; Eyre H J; Whitmore S A; Sutherland G R; Callen D F
C16orf5, a novel proline-rich gene at 16p13.3, is highly expressed in the brain.
Journal of human genetics 1999;44(6):383-7.
1998: Centola M; Chen X; Sood R; Deng Z; Aksentijevich I; Blake T; Ricke D O; Chen X; Wood G; Zaks N; Richards N; Krizman D; Mansfield E; Apostolou S; Liu J; Shafran N; Vedula A; Hamon M; Cercek A; Kahan T; Gumucio D; Callen D F; Richards R I; Moyzis R K; Doggett N A; Collins F S; Liu P P; Fischel-Ghodsian N; Kastner D L
Construction of an approximately 700-kb transcript map around the familial Mediterranean fever locus on human chromosome 16p13.3.
Genome research 1998;8(11):1172-91.
1998: Whitmore S A; Settasatian C; Crawford J; Lower K M; McCallum B; Seshadri R; Cornelisse C J; Moerland E W; Cleton-Jansen A M; Tipping A J; Mathew C G; Savnio M; Savoia A; Verlander P; Auerbach A D; Van Berkel C; Pronk J C; Doggett N A; Callen D F
Characterization and screening for mutations of the growth arrest-specific 11 (GAS11) and C16orf3 genes at 16q24.3 in breast cancer.
Genomics 1998;52(3):325-31.
1998: Kuss B J; O'Neill G M; Eyre H; Doggett N A; Callen D F; Davey R A
ARA, a novel ABC transporter, is located at 16p13.1, is deleted in inv(16) leukemias, and is shown to be expressed in primitive hematopoietic precursors.
Genomics 1998;51(3):455-8.
1998: Cavanaugh J A; Callen D F; Wilson S R; Stanford P M; Sraml M E; Gorska M; Crawford J; Whitmore S A; Shlegel C; Foote S; Kohonen-Corish M; Pavli P
Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16.
Annals of human genetics 1998;62(Pt 4):291-8.
1998: Whitmore S A; Crawford J; Apostolou S; Eyre H; Baker E; Lower K M; Settasatian C; Goldup S; Seshadri R; Gibson R A; Mathew C G; Cleton-Jansen A M; Savoia A; Pronk J C; Auerbach A D; Doggett N A; Sutherland G R; Callen D F
Construction of a high-resolution physical and transcription map of chromosome 16q24.3: a region of frequent loss of heterozygosity in sporadic breast cancer.
Genomics 1998;50(1):1-8.
1998: Kremmidiotis G; Baker E; Crawford J; Eyre H J; Nahmias J; Callen D F
Localization of human cadherin genes to chromosome regions exhibiting cancer-related loss of heterozygosity.
Genomics 1998;49(3):467-71.
1998: Town M; Jean G; Cherqui S; Attard M; Forestier L; Whitmore S A; Callen D F; Gribouval O; Broyer M; Bates G P; van't Hoff W; Antignac C
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis.
Nature genetics 1998;18(4):319-24.
1998: Schollen E; Pardon E; Heykants L; Renard J; Doggett N A; Callen D F; Cassiman J J; Matthijs G
Comparative analysis of the phosphomannomutase genes PMM1, PMM2 and PMM2psi: the sequence variation in the processed pseudogene is a reflection of the mutations found in the functional gene.
Human molecular genetics 1998;7(2):157-64.
1997: Fang Y Y; Bain S; Haan E A; Eyre H J; MacDonald M; Wright T J; Altherr M R; Riess O; Sutherland G; Callen D F
High resolution characterization of an interstitial deletion of less than 1.9 Mb at 4p16.3 associated with Wolf-Hirschhorn syndrome.
American journal of medical genetics 1997;71(4):453-7.
1997: Sood R; Blake T; Aksentijevich I; Wood G; Chen X; Gardner D; Shelton D A; Mangelsdorf M; Orsborn A; Pras E; Balow J E; Centola M; Deng Z; Zaks N; Chen X; Richards N; Fischel-Ghodsian N; Rotter J I; Pras M; Shohat M; Deaven L L; Gumucio D L; Callen D F; Richards R I; Doggett N A
Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3.
Genomics 1997;42(1):83-95.
1997: Ianzano L; D'Apolito M; Centra M; Savino M; Levran O; Auerbach A D; Cleton-Jansen A M; Doggett N A; Pronk J C; Tipping A J; Gibson R A; Mathew C G; Whitmore S A; Apostolou S; Callen D F; Zelante L; Savoia A
The genomic organization of the Fanconi anemia group A (FAA) gene.
Genomics 1997;41(3):309-14.
1997: Callen D F; Yip M Y; Eyre H J
Rapid detection of euchromatin by Alu-PRINS: use in clinical cytogenetics.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 1997;5(2):81-5.
1997: Mitchison H M; Munroe P B; O'Rawe A M; Taschner P E; de Vos N; Kremmidiotis G; Lensink I; Munk A C; D'Arigo K L; Anderson J W; Lerner T J; Moyzis R K; Callen D F; Breuning M H; Doggett N A; Gardiner R M; Mole S E
Genomic structure and complete nucleotide sequence of the Batten disease gene, CLN3.
Genomics 1997;40(2):346-50.
1997: Mitchison H M; Taschner P E; Kremmidiotis G; Callen D F; Doggett N A; Lerner T J; Janes R B; Wallace B A; Munroe P B; O'Rawe A M; Gardiner R M; Mole S E
Structure of the CLN3 gene and predicted structure, location and function of CLN3 protein.
Neuropediatrics 1997;28(1):12-4.
1996: Foe J R; Rooimans M A; Bosnoyan-Collins L; Alon N; Wijker M; Parker L; Lightfoot J; Carreau M; Callen D F; Savoia A; Cheng N C; van Berkel C G; Strunk M H; Gille J J; Pals G; Kruyt F A; Pronk J C; Arwert F; Buchwald M; Joenje H
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.
Nature genetics 1996;14(4):488.
1996: Lo Ten Foe J R; Rooimans M A; Bosnoyan-Collins L; Alon N; Wijker M; Parker L; Lightfoot J; Carreau M; Callen D F; Savoia A; Cheng N C; van Berkel C G; Strunk M H; Gille J J; Pals G; Kruyt F A; Pronk J C; Arwert F; Buchwald M; Joenje H
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA.
Nature genetics 1996;14(3):320-3.
1996: Kuss B J; Deeley R G; Cole S P; Willman C L; Kopecky K J; Wolman S R; Eyre H J; Callen D F
The biological significance of the multidrug resistance gene MRP in inversion 16 leukemias.
Leukemia & lymphoma 1996;20(5-6):357-64.
1996: Wilton S D; Lim L; Dorosz S D; Gunn H C; Eyre H J; Callen D F; Laing N G
Assignment of the human alpha-tropomyosin gene TPM4 to band 19p13.1 by fluorescence in situ hybridization.
Cytogenetics and cell genetics 1996;72(4):294-6.
1996: Doggett N A; Breuning M H; Callen D F
Report of the fourth international workshop on human chromosome 16 mapping 1995.
Cytogenetics and cell genetics 1996;72(4):271-93.
1995: Fang Y Y; Eyre H J; Bohlander S K; Estop A; McPherson E; Träger T; Riess O; Callen D F
Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4.
American journal of human genetics 1995;57(5):1137-42.
1995: Callen D F; Lane S A; Kozman H; Kremmidiotis G; Whitmore S A; Lowenstein M; Doggett N A; Kenmochi N; Page D C; Maglott D R
Integration of transcript and genetic maps of chromosome 16 at near-1-Mb resolution: demonstration of a "hot spot" for recombination at 16p12.
Genomics 1995;29(2):503-11.
1995: Järvelä I E; Mitchison H M; O'Rawe A M; Munroe P B; Taschner P E; de Vos N; Lerner T J; D'Arigo K L; Callen D F; Thompson A D
YAC and cosmid contigs spanning the Batten disease (CLN3) region at 16p12.1-p11.2.
Genomics 1995;29(2):478-89.
1995: Dooley T P; Probst P; Obermoeller R D; Siciliano M J; Doggett N A; Callen D F; Mitchison H M; Mole S E
Phenol sulfotransferases: candidate genes for Batten disease.
American journal of medical genetics 1995;57(2):327-32.
1995: Järvelä I E; Mitchison H M; Callen D F; Lerner T J; Doggett N A; Taschner P E; Gardiner R M; Mole S E
Physical map of the region containing the gene for Batten disease (CLN3).
American journal of medical genetics 1995;57(2):316-9.
1995: Taschner P E; de Vos N; Thompson A D; Callen D F; Doggett N; Mole S E; Dooley T P; Barth P G; Breuning M H
Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease).
American journal of human genetics 1995;56(3):663-8.
1995: Callen D F; Eyre H J; Dolman G; Garry-Battersby M B; McCreanor J R; Valeba A; McGill J J
Molecular cytogenetic characterisation of a small ring X chromosome in a Turner patient and in a male patient with congenital abnormalities: role of X inactivation.
Journal of medical genetics 1995;32(2):113-6.
1995: Cleton-Jansen A M; Moerland H W; Callen D F; Doggett N A; Devilee P; Cornelisse C J
Mapping of the breast basic conserved gene (D16S444E) to human chromosome band 16q24.3.
Cytogenetics and cell genetics 1995;68(1-2):49-51.
1995: Doggett N A; Callen D F
Report and abstracts of the third international workshop on human chromosome 16 mapping 1994. Pittsburgh, Pennsylvania, May 7-9, 1994.
Cytogenetics and cell genetics 1995;68(3-4):165-84.
1995: Hunt C C; Eyre H J; Akkari P A; Meredith C; Dorosz S M; Wilton S D; Callen D F; Laing N G; Baker E
Assignment of the human beta tropomyosin gene (TPM2) to band 9p13 by fluorescence in situ hybridisation.
Cytogenetics and cell genetics 1995;71(1):94-5.
1994: Dooley T P; Mitchison H M; Munroe P B; Probst P; Neal M; Siciliano M J; Deng Z; Doggett N A; Callen D F; Gardiner R M
Mapping of two phenol sulphotransferase genes, STP and STM, to 16p: candidate genes for Batten disease.
Biochemical and biophysical research communications 1994;205(1):482-9.
1994: Schultz E A; Callen D F; Doggett N A; Haines J L; Lerner T J
Microsatellite repeat polymorphism at the D16S366 locus.
Human molecular genetics 1994;3(9):1713.
1994: Maglott D R; Durkin A S; Lane S A; Callen D F; Feldblyum T V; Nierman W C
The gene for membrane protein E16 (D16S469E) maps to human chromosome 16q24.3 and is expressed in human brain, thymus, and retina.
Genomics 1994;23(1):303-4.
1994: Nancarrow J K; Kremer E; Holman K; Eyre H; Doggett N A; Le Paslier D; Callen D F; Sutherland G R; Richards R I
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis.
Science (New York, N.Y.) 1994;264(5167):1938-41.
1994: Garnham I W; Fernandez H; Callen D F; Haan E A; Sutherland G R
Discordance between direct and PHA-stimulated chromosome preparations from neonates.
Clinical genetics 1994;45(6):277-80.
1994: Whitmore S A; Apostolou S; Lane S; Nancarrow J K; Phillips H A; Richards R I; Sutherland G R; Callen D F
Isolation and characterization of transcribed sequences from a chromosome 16 hn-cDNA library and the physical mapping of genes and transcribed sequences using a high-resolution somatic cell panel of human chromosome 16.
Genomics 1994;20(2):169-75.
1994: Cleton-Jansen A M; Moerland E W; Kuipers-Dijkshoorn N J; Callen D F; Sutherland G R; Hansen B; Devilee P; Cornelisse C J
At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer.
Genes, chromosomes & cancer 1994;9(2):101-7.
1994: Cleton-Jansen A M; Moerland H W; Vossen R H; Callen D F; Breuning M H; Devilee P
Dinucleotide repeat polymorphism at D16S533.
Human molecular genetics 1994;3(1):216.
1994: Shen Y; Holman K; Doggett N A; Callen D F; Sutherland G R; Richards R I
Dinucleotide repeat polymorphisms at the D16S525, D16S359, D16S531 and D16S522 loci.
Human molecular genetics 1994;3(1):210.
1994: Akkari P A; Eyre H J; Wilton S D; Callen D F; Lane S A; Meredith C; Kedes L; Laing N G
Assignment of the human skeletal muscle alpha actin gene (ACTA1) to 1q42 by fluorescence in situ hybridisation.
Cytogenetics and cell genetics 1994;65(4):265-7.
1994: Callen D F
Characterization of constitutive marker chromosomes in humans.
Methods in molecular biology (Clifton, N.J.) 1994;33():439-57.
1993: Doggett N A; Callen D F; Chen Z L; Moore S; Tesmer J G; Duesing L A; Stallings R L
Identification and regional localization of a human IMP dehydrogenase-like locus (IMPDHL1) at 16p13.13.
Genomics 1993;18(3):687-9.
1993: Shen Y; Holman K; Doggett N A; Callen D F; Sutherland G R; Richards R I
Four dinucleotide repeat polymorphisms on human chromosome 16.
Human molecular genetics 1993;2(10):1745.
1993: Callen D F; Eyre H; Lane S; Shen Y; Hansmann I; Spinner N; Zackai E; McDonald-McGinn D; Schuffenhauer S; Wauters J
High resolution mapping of interstitial long arm deletions of chromosome 16: relationship to phenotype.
Journal of medical genetics 1993;30(10):828-32.
1993: Williams R; Vesa J; Järvelä I; McKay T; Mitchison H; Hellsten E; Thompson A; Callen D; Sutherland G; Luna-Battadano D
Genetic heterogeneity in neuronal ceroid lipofuscinosis (NCL): evidence that the late-infantile subtype (Jansky-Bielschowsky disease; CLN2) is not an allelic form of the juvenile or infantile subtypes.
American journal of human genetics 1993;53(4):931-5.
1993: Shen Y; Holman K; Doggett N A; Callen D F; Sutherland G R; Richards R I
Three dinucleotide repeat polymorphisms on human chromosome 16p13.11-p13.3.
Human molecular genetics 1993;2(9):1506.
1993: Shen Y; Holman K; Doggett N A; Callen D F; Sutherland G R; Richards R I
Six dinucleotide repeat polymorphisms on human chromosome 16q12.1-q24.1.
Human molecular genetics 1993;2(9):1505.
1993: Shen Y; Holman K; Doggett N A; Callen D F; Sutherland G R; Richards R I
Five dinucleotide repeat polymorphisms on human chromosome 16q24.2-q24.3.
Human molecular genetics 1993;2(9):1504.
1993: Callen D F; Thompson A D; Shen Y; Phillips H A; Richards R I; Mulley J C; Sutherland G R
Incidence and origin of "null" alleles in the (AC)n microsatellite markers.
American journal of human genetics 1993;52(5):922-7.
1993: Mitchison H M; Thompson A D; Mulley J C; Kozman H M; Richards R I; Callen D F; Stallings R L; Doggett N A; Attwood J; McKay T R
Fine genetic mapping of the Batten disease locus (CLN3) by haplotype analysis and demonstration of allelic association with chromosome 16p microsatellite loci.
Genomics 1993;16(2):455-60.
1993: Baker E; Guo X H; Orsborn A M; Sutherland G R; Callen D F; Hopwood J J; Morris C P
The morquio A syndrome (mucopolysaccharidosis IVA) gene maps to 16q24.3.
American journal of human genetics 1993;52(1):96-8.
1993: Kozman H M; Phillips H A; Callen D F; Sutherland G R; Mulley J C
Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic loci.
Cytogenetics and cell genetics 1993;62(4):194-8.
1993: Mitchison H M; Williams R E; McKay T R; Callen D F; Thompson A D; Mulley J C; Stallings R L; Hildebrand C E; Moyzis R K; Järvelä I
Refined genetic mapping of juvenile-onset neuronal ceroid-lipofuscinosis on chromosome 16.
Journal of inherited metabolic disease 1993;16(2):339-41.
1992: Shen Y; Thompson A T; Holman K; Callen D F; Sutherland G R; Richards R I
Four dinucleotide repeat polymorphisms on human chromosome 16 at D16S289, D16S318, D16S319 and D16S320.
Human molecular genetics 1992;1(9):773.
1992: Fietz M J; Rogers G E; Eyre H J; Baker E; Callen D F; Sutherland G R
Mapping of the trichohyalin gene: co-localization with the profilaggrin, involucrin, and loricrin genes.
The Journal of investigative dermatology 1992;99(5):542-4.
1992: Callen D F; Doggett N A; Stallings R L; Chen L Z; Whitmore S A; Lane S A; Nancarrow J K; Apostolou S; Thompson A D; Lapsys N M
High-resolution cytogenetic-based physical map of human chromosome 16.
Genomics 1992;13(4):1178-85.
1992: Stallings R L; Doggett N A; Callen D; Apostolou S; Chen L Z; Nancarrow J K; Whitmore S A; Harris P; Michison H; Breuning M
Evaluation of a cosmid contig physical map of human chromosome 16.
Genomics 1992;13(4):1031-9.
1992: Callen D F; Eyre H; Yip M Y; Freemantle J; Haan E A
Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes.
American journal of medical genetics 1992;43(4):709-15.
1992: Thompson A D; Shen Y; Holman K; Sutherland G R; Callen D F; Richards R I
Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16.
Genomics 1992;13(2):402-8.
1992: Kremer E J; Kalatzis V; Baker E; Callen D F; Sutherland G R; Maliszewski C R
The gene for the human IgA Fc receptor maps to 19q13.4.
Human genetics 1992;89(1):107-8.
1992: Pritchard M A; Baker E; Callen D F; Sutherland G R; Wilks A F
Two members of the JAK family of protein tyrosine kinases map to chromosomes 1p31.3 and 9p24.
Mammalian genome : official journal of the International Mammalian Genome Society 1992;3(1):36-8.
1992: Lapsys N M; Layfield R; Baker E; Callen D F; Sutherland G R; Abedinia M; Nixon P F; Mattick J S
Chromosomal location of the human transketolase gene.
Cytogenetics and cell genetics 1992;61(4):274-5.
1992: Shen Y; Baker E; Callen D F; Sutherland G R; Willson T A; Rakar S; Gough N M
Localization of the human GM-CSF receptor beta chain gene (CSF2RB) to chromosome 22q12.2-->q13.1.
Cytogenetics and cell genetics 1992;61(3):175-7.
1992: Callen D F; Hildebrand C E; Reeders S
Report of the Second International Workshop on Human Chromosome 16 Mapping.
Cytogenetics and cell genetics 1992;60(3-4):158-67.
1991: Phillips H A; Hyland V J; Holman K; Callen D F; Richards R I; Mulley J C
Dinucleotide repeat polymorphism at D16S287.
Nucleic acids research 1991;19(23):6664.
1991: Callen D F; Baker E; Lane S; Nancarrow J; Thompson A; Whitmore S A; MacLennan D H; Berger R; Cherif D; Järvelä I
Regional mapping of the Batten disease locus (CLN3) to human chromosome 16p12.
American journal of human genetics 1991;49(6):1372-7.
1991: Kozman H M; Gedeon A K; Whitmore S; Suthers G K; Callen D F; Sutherland G R; Mulley J C
Addition of MT, D16S10, D16S4, and D16S91 to the linkage map within 16q12.1-q22.1.
Genomics 1991;11(3):756-9.
1991: Chen L Z; Shen Y; Holman K; Thompson A; Lane S; Richards R I; Sutherland G R; Callen D F
An STS at the D16S290 locus.
Nucleic acids research 1991;19(20):5793.
1991: Shen Y; Holman K; Thompson A; Kozman H; Callen D F; Sutherland G R; Richards R I
Dinucleotide repeat polymorphism at the D16S288 locus.
Nucleic acids research 1991;19(19):5445.
1991: Richards R I; Holman K; Lane S; Sutherland G R; Callen D F
Human chromosome 16 physical map: mapping of somatic cell hybrids using multiplex PCR deletion analysis of sequence tagged sites.
Genomics 1991;10(4):1047-52.
1991: Callen D F; Fernandez H; Hull Y J; Svigos J M; Chambers H M; Sutherland G R
A normal 46,XX infant with a 46,XX/69,XXY placenta: a major contribution to the placenta is from a resorbed twin.
Prenatal diagnosis 1991;11(7):437-42.
1991: Callen D F; Eyre H J; Ringenbergs M L; Freemantle C J; Woodroffe P; Haan E A
Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.
American journal of human genetics 1991;48(4):769-82.
1991: Wilson P J; Suthers G K; Callen D F; Baker E; Nelson P V; Cooper A; Wraith J E; Sutherland G R; Morris C P; Hopwood J J
Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome.
Human genetics 1991;86(5):505-8.
1991: Callen D F; Hull Y J; Toogood I R; Fioretos T; Heim S; Mandahl N; Mitelman F
New chromosomal rearrangement, t(12;22)(p13;q12), in acute nonlymphocytic leukemia.
Cancer genetics and cytogenetics 1991;51(2):255-8.
1991: MacKinnon P J; Powell B C; Rogers G E; Baker E G; MacKinnon R N; Hyland V J; Callen D F; Sutherland G R
An ultrahigh-sulphur keratin gene of the human hair cuticle is located at 11q13 and cross-hybridizes with sequences at 11p15.
Mammalian genome : official journal of the International Mammalian Genome Society 1991;1(1):53-6.
1991: Baker E; Chen L Z; Smith C A; Callen D F; Goodwin R; Sutherland G R
Chromosomal location of the human tumor necrosis factor receptor genes.
Cytogenetics and cell genetics 1991;57(2-3):117-8.
1990: Scott H S; Ashton L J; Eyre H J; Baker E; Brooks D A; Callen D F; Sutherland G R; Morris C P; Hopwood J J
Chromosomal localization of the human alpha-L-iduronidase gene (IDUA) to 4p16.3.
American journal of human genetics 1990;47(5):802-7.
1990: Breuning M H; Snijdewint F G; Brunner H; Verwest A; Ijdo J W; Saris J J; Dauwerse J G; Blonden L; Keith T; Callen D F
Map of 16 polymorphic loci on the short arm of chromosome 16 close to the polycystic kidney disease gene (PKD1).
Journal of medical genetics 1990;27(10):603-13.
1990: Callen D F; Freemantle C J; Ringenbergs M L; Baker E; Eyre H J; Romain D; Haan E A
The isochromosome 18p syndrome: confirmation of cytogenetic diagnosis in nine cases by in situ hybridization.
American journal of human genetics 1990;47(3):493-8.
1990: Suthers G K; Hyland V J; Callen D F; Oberle I; Rocchi M; Thomas N S; Morris C P; Schwartz C E; Schmidt M; Ropers H H
Physical mapping of new DNA probes near the fragile X mutation (FRAXA) by using a panel of cell lines.
American journal of human genetics 1990;47(2):187-95.
1990: Callen D F; Ringenbergs M L; Fowler J C; Freemantle C J; Haan E A
Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.
Journal of medical genetics 1990;27(3):155-9.
1990: Callen D F; Eyre H J; Ringenbergs M L
A dicentric variant of chromosome 6: characterization by use of in situ hybridisation with the biotinylated probe p308.
Clinical genetics 1990;37(2):81-3.
1990: Hyland V J; Suthers G K; Friend K; MacKinnon R N; Callen D F; Breuning M H; Keith T; Brown V A; Phipps P; Sutherland G R
Probe, VK5B, is located in the same interval as the autosomal dominant adult polycystic kidney disease locus, PKD1.
Human genetics 1990;84(3):286-8.
1990: Sutherland G R; Baker E; Callen D F; Garson O M; West A K
The human metallothionein gene cluster is not disrupted in myelomonocytic leukemia.
Genomics 1990;6(1):144-8.
1990: Mulley J C; Barton N; Callen D F
Localisation of human PGP and HAGH genes to 16p13.3.
Cytogenetics and cell genetics 1990;53(2-3):175-6.
1990: Callen D F; Baker E; Eyre H J; Chernos J E; Bell J A; Sutherland G R
Reassessment of two apparent deletions of chromosome 16p to an ins(11;16) and a t(1;16) by chromosome painting.
Annales de génétique 1990;33(4):219-21.
1990: Callen D F; Baker E; Eyre H J; Lane S A
An expanded mouse-human hybrid cell panel for mapping human chromosome 16.
Annales de génétique 1990;33(4):190-5.
1989: Suthers G K; Callen D F; Hyland V J; Kozman H M; Baker E; Eyre H; Harper P S; Roberts S H; Hors-Cayla M C; Davies K E
A new DNA marker tightly linked to the fragile X locus (FRAXA).
Science (New York, N.Y.) 1989;246(4935):1298-300.
1989: Callen D F; Raphael K; Michael P M; Garson O M
Acute lymphoblastic leukemia with a hypodiploid karyotype with less than 40 chromosomes: the basis for division into two subgroups.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(10):749-52.
1989: Fowler J C; Burgoyne L A; Baker E G; Ringenbergs M L; Callen D F
Human satellite III DNA: genomic location and sequence homogeneity of the TaqI-deficient polymorphic sequences.
Chromosoma 1989;98(4):266-72.
1989: Hyland V J; Fernandez K E; Callen D F; MacKinnon R N; Baker E; Friend K; Sutherland G R
Assignment of anonymous DNA probes to specific intervals of human chromosomes 16 and X.
Human genetics 1989;83(1):61-6.
1989: Sutherland G R; Baker E; Fernandez K E; Callen D F; Goodwin R G; Lupton S; Namen A E; Shannon M F; Vadas M A
The gene for human interleukin 7 (IL7) is at 8q12-13.
Human genetics 1989;82(4):371-2.
1989: Callen D F; Cirocco L; Moore L
A der(11)t(8;11) in two medulloblastomas. A possible nonrandom cytogenetic abnormality.
Cancer genetics and cytogenetics 1989;38(2):255-60.
1989: Callen D F; Hyland V J; Baker E G; Fratini A; Gedeon A K; Mulley J C; Fernandez K E; Breuning M H; Sutherland G R
Mapping the short arm of human chromosome 16.
Genomics 1989;4(3):348-54.
1989: Litjens T; Baker E G; Beckmann K R; Morris C P; Hopwood J J; Callen D F
Chromosomal localization of ARSB, the gene for human N-acetylgalactosamine-4-sulphatase.
Human genetics 1989;82(1):67-8.
1989: Sutherland G R; Baker E; Hyland V J; Callen D F; Stahl J; Gough N M
The gene for human leukemia inhibitory factor (LIF) maps to 22q12.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 1989;3(1):9-13.
1989: Sutherland G R; Baker E; Fernandez K E; Callen D F; Aldred P; Coghlan J P; Wright R D; Fernley R T
The gene for human carbonic anhydrase VI(CA6) is on the tip of the short arm of chromosome 1.
Cytogenetics and cell genetics 1989;50(2-3):149-50.
1988: Suthers G K; Hyland V J; Baker E; Fernandez K E; Callen D F; Sutherland G R
TaqI RFLP identified by probe VK17A (DXS294) at Xq26.
Nucleic acids research 1988;16(23):11389.
1988: Sutherland G R; Baker E; Callen D F; Hyland V J; May B K; Bawden M J; Healy H M; Borthwick I A
5-Aminolevulinate synthase is at 3p21 and thus not the primary defect in X-linked sideroblastic anemia.
American journal of human genetics 1988;43(3):331-5.
1988: Fratini A; Baker E G; Callen D F; Hyland V J; Sutherland G R
RsaI and TaqI RFLPs for pACHF3.5 [D16S10].
Nucleic acids research 1988;16(18):9066.
1988: Fratini A; Baker E G; Callen D F; Reeders S; Hyland V J; Sutherland G R
pACHF1.1 [D16S8] detects a common PvuII RFLP and maps at 16p13.3----16p13.11.
Nucleic acids research 1988;16(18):9065.
1988: Fratini A; Baker E G; Callen D F; Hyland V J; Sutherland G R
ACHF249 [D22S14] detects a common PstI RFLP and maps at 22cen----22q13.1.
Nucleic acids research 1988;16(18):9064.
1988: Sutherland G R; Baker E; Callen D F; Hyland V J; Wong G; Clark S; Jones S S; Eglinton L K; Shannon M F; Lopez A F
Interleukin 4 is at 5q31 and interleukin 6 is at 7p15.
Human genetics 1988;79(4):335-7.
1988: Callen D F; Korban G; Dawson G; Gugasyan L; Krumins E J; Eichenbaum S; Petrass J; Purvis-Smith S; Smith A; Den Dulk G
Extra embryonic/fetal karyotypic discordance during diagnostic chorionic villus sampling.
Prenatal diagnosis 1988;8(6):453-60.
1988: Robertson D A; Callen D F; Baker E G; Morris C P; Hopwood J J
Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14.
Human genetics 1988;79(2):175-8.
1988: Sutherland G R; Baker E; Callen D F; Campbell H D; Young I G; Sanderson C J; Garson O M; Lopez A F; Vadas M A
Interleukin-5 is at 5q31 and is deleted in the 5q- syndrome.
Blood 1988;71(4):1150-2.
1988: Puspurs A H; Baker E; Callen D F; Fratini A; Sutherland G R
Translocation breakpoint in t(11;14) in B-cell leukemia is not at the rare fragile site at 11q13.3.
Cancer genetics and cytogenetics 1988;31(1):25-30.
1988: Hyland V J; Grist S; Callen D F; Sutherland G R
Anonymous DNA probes to human chromosome 16 derived from a flow-purified library.
American journal of human genetics 1988;42(2):373-9.
1988: Callen D F; Hyland V J; Baker E G; Fratini A; Simmers R N; Mulley J C; Sutherland G R
Fine mapping of gene probes and anonymous DNA fragments to the long arm of chromosome 16.
Genomics 1988;2(2):144-53.
1988: Sutherland G R; Baker E; Callen D F
A BrdU-enhanceable fragile site or viral modification site at 11q23.1 in lymphoblastoid cultures.
Cytogenetics and cell genetics 1988;47(4):201-3.
1988: Sutherland G R; Baker E; Hyland V J; Callen D F; Close J A; Tregear G W; Evans B A; Richards R I
Human prostate-specific antigen (APS) is a member of the glandular kallikrein gene family at 19q13.
Cytogenetics and cell genetics 1988;48(4):205-7.
1987: Simmers R N; Mulley J C; Hyland V J; Callen D F; Sutherland G R
Mapping the human alpha globin gene complex to 16p13.2----pter.
Journal of medical genetics 1987;24(12):761-6.
1987: Callen D F; Mulley J C; Baker E G; Sutherland G R
Determining the origin of human X isochromosomes by use of DNA sequence polymorphisms and detection of an apparent i(Xq) with Xp sequences.
Human genetics 1987;77(3):236-40.
1987: Callen D F; Baker E; Simmers R N; Seshadri R; Roninson I B
Localization of the human multiple drug resistance gene, MDR1, to 7q21.1.
Human genetics 1987;77(2):142-4.
1987: Sutherland G R; Reeders S; Hyland V J; Callen D F; Fratini A; Mulley J C
Molecular genetics of human chromosome 16.
Journal of medical genetics 1987;24(8):451-6.
1987: Callen D F; Sutherland G R; Carter R F
A fertile man with tdic(Y;22): how a stable neo-X1X2Y sex-determining mechanism could evolve in man.
American journal of medical genetics. Supplement 1987;3():151-5.
1986: Fratini A; Simmers R N; Callen D F; Hyland V J; Tischfield J A; Stambrook P J; Sutherland G R
A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23)(FRA16D) loci.
Cytogenetics and cell genetics 1986;43(1-2):10-3.
1985: Michael P M; Garson O M; Callen D F
A review of the t(1;19) breakpoints in acute lymphocytic leukemia.
Cancer genetics and cytogenetics 1985;17(1):79-80.

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