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Melanie Bahlo
Melanie Bahlo
Theme Leader, Healthy Development and Ageing, The Walter and Eliza Hall Institute of
Verified email at wehi.edu.au - Homepage
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Cited by
Cited by
Year
IL28B is associated with response to chronic hepatitis C interferon-α and ribavirin therapy
V Suppiah, M Moldovan, G Ahlenstiel, T Berg, M Weltman, ML Abate, ...
Nature genetics 41 (10), 1100-1104, 2009
23062009
Development of plasmacytoid and conventional dendritic cell subtypes from single precursor cells derived in vitro and in vivo
SH Naik, P Sathe, HY Park, D Metcalf, AI Proietto, A Dakic, S Carotta, ...
Nature immunology 8 (11), 1217-1226, 2007
9342007
Iron-overload–related disease in HFE hereditary hemochromatosis
KJ Allen, LC Gurrin, CC Constantine, NJ Osborne, MB Delatycki, AJ Nicoll, ...
New England Journal of Medicine 358 (3), 221-230, 2008
7842008
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
Data analysis: Bahlo Melanie 2 Brown Matthew A 6 7 Browning Brian L 20 ...
Nature genetics 41 (7), 824-828, 2009
5072009
Strikingly different clinicopathological phenotypes determined by progranulin-mutation dosage
KR Smith, J Damiano, S Franceschetti, S Carpenter, L Canafoglia, ...
The American Journal of Human Genetics 90 (6), 1102-1107, 2012
4282012
Genome‐wide meta‐analysis identifies novel multiple sclerosis susceptibility loci
NA Patsopoulos, ...
Annals of neurology 70 (6), 897-912, 2011
3292011
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy
SE Heron, KR Smith, M Bahlo, L Nobili, E Kahana, L Licchetta, KL Oliver, ...
Nature genetics 44 (11), 1188-1190, 2012
3272012
Array-based gene discovery with three unrelated subjects shows SCARB2/LIMP-2 deficiency causes myoclonus epilepsy and glomerulosclerosis
SF Berkovic, LM Dibbens, A Oshlack, JD Silver, M Katerelos, DF Vears, ...
The American Journal of Human Genetics 82 (3), 673-684, 2008
2842008
Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26
SA Treloar, J Wicks, DR Nyholt, GW Montgomery, M Bahlo, V Smith, ...
The American Journal of Human Genetics 77 (3), 365-376, 2005
2732005
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia—MLASA syndrome
LG Riley, S Cooper, P Hickey, J Rudinger-Thirion, M McKenzie, ...
The American Journal of Human Genetics 87 (1), 52-59, 2010
2542010
The Tasmanian devil transcriptome reveals Schwann cell origins of a clonally transmissible cancer
EP Murchison, C Tovar, A Hsu, HS Bender, P Kheradpour, CA Rebbeck, ...
Science 327 (5961), 84-87, 2010
2542010
Inference from gene trees in a subdivided population
M Bahlo, RC Griffiths
Theoretical population biology 57 (2), 79-95, 2000
2512000
Identification and analysis of error types in high-throughput genotyping
KR Ewen, M Bahlo, SA Treloar, DF Levinson, B Mowry, JW Barlow, ...
The American Journal of Human Genetics 67 (3), 727-736, 2000
2212000
Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathology
GR Wilson, JCH Sim, C McLean, M Giannandrea, CA Galea, JR Riseley, ...
The American Journal of Human Genetics 95 (6), 729-735, 2014
2032014
An α‐E‐catenin (CTNNA1) mutation in hereditary diffuse gastric cancer
IJ Majewski, I Kluijt, A Cats, TS Scerri, D de Jong, RJC Kluin, S Hansford, ...
The Journal of pathology 229 (4), 621-629, 2013
1892013
A Cav3. 2 T-type calcium channel point mutation has splice-variant-specific effects on function and segregates with seizure expression in a polygenic rat model of absence epilepsy
KL Powell, SM Cain, C Ng, S Sirdesai, LS David, M Kyi, E Garcia, ...
Journal of Neuroscience 29 (2), 371-380, 2009
1762009
Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features
D Lessel, B Vaz, S Halder, PJ Lockhart, I Marinovic-Terzic, ...
Nature genetics 46 (11), 1239-1244, 2014
1702014
Kufs disease, the major adult form of neuronal ceroid lipofuscinosis, caused by mutations in CLN6
T Arsov, KR Smith, J Damiano, S Franceschetti, L Canafoglia, ...
The American Journal of Human Genetics 88 (5), 566-573, 2011
1662011
Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians
JP Rubio, J Stankovich, J Field, N Tubridy, M Marriott, C Chapman, ...
Genes & Immunity 9 (7), 624-630, 2008
1542008
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked …
FJ Kaiser, M Ansari, D Braunholz, M Concepción Gil-Rodríguez, ...
Human molecular genetics 23 (11), 2888-2900, 2014
1522014
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