Prof David F Callen
Prof David F Callen
Director of Centre for Personalised Cancer Medicine, University of Adelaide, South Australia
Verified email at
Cited by
Cited by
Incidence and origin of" null" alleles in the (AC) n microsatellite markers.
DF Callen, AD Thompson, Y Shen, HA Phillips, RI Richards, JC Mulley, ...
American journal of human genetics 52 (5), 922, 1993
A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis
M Town, G Jean, S Cherqui, M Attard, L Forestier, SA Whitmore, ...
Nature genetics 18 (4), 319-324, 1998
Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance
MA Tischfield, HN Baris, C Wu, G Rudolph, L Van Maldergem, W He, ...
Cell 140 (1), 74-87, 2010
Expression cloning of a cDNA for the major Fanconi anaemia gene, FAA
JR Lo Ten Foe, MA Rooimans, L Bosnoyan-Collins, N Alon, M Wijker, ...
Nature genetics 14 (3), 320-323, 1996
Derepression of an endogenous long terminal repeat activates the CSF1R proto-oncogene in human lymphoma
B Lamprecht, K Walter, S Kreher, R Kumar, M Hummel, D Lenze, ...
Nature medicine 16 (5), 571-579, 2010
Integration of cytogenetic landmarks into the draft sequence of the human genome
T BAC Resource Consortium, VG Cheung, N Nowak, W Jang, IR Kirsch, ...
Nature 409 (6822), 953-958, 2001
The oncogenic role of miR-155 in breast cancer
S Mattiske, RJ Suetani, PM Neilsen, DF Callen
Cancer epidemiology, biomarkers & prevention 21 (8), 1236-1243, 2012
Localization of the human multiple drug resistance gene, MDR1, to 7q21.1
DF Callen, E Baker, RN Simmers, R Seshadri, IB Roninson
Human genetics 77, 142-144, 1987
A third Wilms' tumor locus on chromosome 16q
MA Maw, PE Grundy, LJ Millow, MR Eccles, RS Dunn, PJ Smith, ...
Cancer research 52 (11), 3094-3098, 1992
The sequence and analysis of duplication-rich human chromosome 16
J Martin, C Han, LA Gordon, A Terry, S Prabhakar, X She, G Xie, ...
Nature 432 (7020), 988-994, 2004
Molecular cloning and physical and genetic mapping of a novel human Na+/H+ exchanger (NHE5/SLC9A5) to chromosome 16q22. 1
CA Klanke, YR Su, DF Callen, Z Wang, P Meneton, N Baird, ...
Genomics 25 (3), 615-622, 1995
Implications of FRA16A structure for the mechanism of chromosomal fragile site genesis
JK Nancarrow, E Kremer, K Holman, H Eyre, NA Doggett, D Le Paslier, ...
Science 264 (5167), 1938-1941, 1994
The NF1 gene revisited–from bench to bedside
YS Yap, JR McPherson, CK Ong, SG Rozen, BT Teh, ASG Lee, DF Callen
Oncotarget 5 (15), 5873, 2014
Mutant p53 drives invasion in breast tumors through up-regulation of miR-155
PM Neilsen, JE Noll, S Mattiske, CP Bracken, PA Gregory, RB Schulz, ...
Oncogene 32 (24), 2992-3000, 2013
Structure and chromosomal localization of the human renal kallikrein gene
BA Evans, ZX Yun, JA Close, GW Tregear, N Kitamura, S Nakanishi, ...
Biochemistry 27 (9), 3124-3129, 1988
The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene
K Bhalla, HA Phillips, J Crawford, OLD McKenzie, JC Mulley, H Eyre, ...
Journal of human genetics 49 (6), 308-311, 2004
At least two different regions are involved in allelic imbalance on chromosome arm 16q in breast cancer
AM Cleton‐Jansen, EW Moerland, NJ Kuipers‐Dijkshoorn, CJ Cornelisse, ...
Genes, Chromosomes and Cancer 9 (2), 101-107, 1994
Study of 250 children with idiopathic mental retardation reveals nine cryptic and diverse subtelomeric chromosome anomalies
E Baker, L Hinton, DF Callen, M Altree, A Dobbie, HJ Eyre, GR Sutherland, ...
American journal of medical genetics 107 (4), 285-293, 2002
Chromosomal origin of small ring marker chromosomes in man: characterization by molecular genetics.
DF Callen, HJ Eyre, ML Ringenbergs, CJ Freemantle, P Woodroffe, ...
American journal of human genetics 48 (4), 769, 1991
Mutations in KCNT1 cause a spectrum of focal epilepsies
RS Møller, SE Heron, LHG Larsen, CX Lim, MG Ricos, MA Bayly, ...
Epilepsia 56 (9), e114-e120, 2015
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