Melanie Bahlo
Melanie Bahlo
Theme Leader, Healthy Development and Ageing, The Walter and Eliza Hall Institute of
Verified email at wehi.edu.au - Homepage
TitleCited byYear
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, 2009
21182009
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, 2007
7252007
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
6362008
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
Australia and New Zealand Multiple Sclerosis Genetics Consortium
Nature genetics 41 (7), 824, 2009
4262009
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
2812012
Genome‐wide meta‐analysis identifies novel multiple sclerosis susceptibility loci
NA Patsopoulos, ...
Annals of neurology 70 (6), 897-912, 2011
2652011
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, 2012
2452012
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
2362005
Inference from gene trees in a subdivided population
M Bahlo, RC Griffiths
Theoretical population biology 57 (2), 79-95, 2000
2342000
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
2312008
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
2112010
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
2052000
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
1972010
Genome-wide linkage analysis of the acute coronary syndrome suggests a locus on chromosome 2
SB Harrap, KS Zammit, ZYH Wong, FM Williams, M Bahlo, AM Tonkin, ...
Arteriosclerosis, thrombosis, and vascular biology 22 (5), 874-878, 2002
1462002
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
1352009
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 and immunity 9 (7), 624, 2008
1352008
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
1232011
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
1112014
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
1112013
Human and mouse mutations in WDR35 cause short-rib polydactyly syndromes due to abnormal ciliogenesis
P Mill, PJ Lockhart, E Fitzpatrick, HS Mountford, EA Hall, MAM Reijns, ...
The American Journal of Human Genetics 88 (4), 508-515, 2011
1102011
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