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Melanie Bahlo

Walter and Eliza Hall Institute of Medical Research

76H-index
477Paper Count
2.1WCitation Count
Published Papers 202
Publication Date
Correction: Patient induced pluripotent stem cells identify specificities of a reticular pseudodrusen phenotype in age-related macular degeneration
err2026-07-22
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errOAAI
errJenna C. Hall; Kavitha Krishna Sudhakar; Maciej Daniszewski; Anne Senabouth; Carla J. Abbott; Helena H. Liang; Himeesh Kumar; Grace E. Lidgerwood; Mehdi Mirzaei; Jessica YW Ma; Trevor Atkeson; Yumiko Hirokawa; Emeline F. Nandrot; Alexander Barnett; Chantal Cazevieille; Gaël Manes; Simon Mountford; Philip Thompson; Erica L. Fletcher; Zhichao Wu; Melanie Bahlo; Brendan R. E. Ansell; Daniel Paull; Alex W. Hewitt; Robyn H. Guymer; Joseph E. Powell; Alice Pébay
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Defining a tandem repeat catalog and variation clusters for genome-wide analyses and population databases
err2026-04-22
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PREAI
errBen Weisburd; Egor Dolzhenko; Mark F. Bennett; Matt C. Danzi; Isaac R.L. Xu; Hope Tanudisastro; Bida Gu; Adam English; Laurel Hiatt; Tom Mokveld; Guilherme De Sena Brandine; Readman Chiu; Nehir Edibe Kurtas; Helyaneh Ziaei Jam; Harrison Brand; Indhu-Shree Rajan-Babu; Melanie Bahlo; Mark J.P. Chaisson; Stephan Züchner; Melissa Gymrek
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Understanding Plasmodium vivax recurrent infections using an amplicon deep sequencing assay, identity-by-descent and model-based classification
err2026-04-18
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errOAAI
errJason Rosado; Jiru Han; Thomas Obadia; Jacob Munro; Zeinabou Traore; Kael Schoffer; Jessica Brewster; Caitlin Bourke; Joseph M. Vinetz; Aimee R. Taylor; Michael White; Melanie Bahlo; Dionicia Gamboa; Ivo Mueller; Shazia Ruybal-Pesántez
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HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvement
err2025-12-08
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errOAAI
errSamaneh Farashi; Carla J. Abbott; Brendan R. E. Ansell; Zhichao Wu; Lebriz Altay; Ella Arnon; Louis Arnould; Yelena Bagdasarova; Konstantinos Balaskas; Fred K. Chen; Emily Chew; Itay Chowers; Steven Clarke; Catherine Cukras; Cécile Delcourt; Marie-Noëlle Delyfer; Anneke I. den Hollander; Sascha Fauser; Robert P. Finger; Pierre-Henry Gabrielle; Jiru Han; Lauren A. B. Hodgson; Ruth Hogg; Frank G. Holz; Carel Hoyng; Himeesh Kumar; Eleonora M. Lad; Aaron Lee; Ulrich F. O. Luhmann; Matthias M. Mauschitz; Amy J. McKnight; Samuel McLenachan; Aniket Mishra; Ismail Moghul; Luz D. Orozco; Danuta M. Sampson; Liam W. Scott; Vasilena Sitnilska; Scott Song; Amy Stockwell; Anand Swaroop; Jan H. Terheyden; Liran Tiosano; Adnan Tufail; Brian L. Yaspan; Alice Pébay; Erica L. Fletcher; Robyn H. Guymer; Melanie Bahlo
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Epilepsy concordance in monozygotic twins: the role of common genetic variants
errBRAIN
IF11.7
err2025-12-01
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PREAI
errDang, Yew Li; Oliver, Karen L.; Esnault, Kate; Bahlo, Melanie; Perucca, Piero; Berkovic, Samuel F.
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Identification of expanded and interrupted ATXN2 repeat expansions in Parkinson’s disease and Lewy Body Dementia cohorts
err2025-11-27
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errOAAI
errLongfei Wang; Michael Milton; Liam G. Fearnley; Oneil G. Bhalala; Melanie Bahlo; Haloom Rafehi
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Deep Learning-Based Detection of Reticular Pseudodrusen in Age-Related Macular Degeneration
err2025-09-08
err0
errOAAI
errHimeesh Kumar; Yelena Bagdasarova; Scott Song; Doron G. Hickey; Amy C. Cohn; Mali Okada; Robert P. Finger; Jan H. Terheyden; Ruth E. Hogg; Pierre-Henry Gabrielle; Louis Arnould; Maxime Jannaud; Xavier Hadoux; Peter van Wijngaarden; Carla J. Abbott; Lauren A. B. Hodgson; Roy Schwartz; Adnan Tufail; Emily Y. Chew; Cecilia S. Lee; Erica L. Fletcher; Melanie Bahlo; Brendan R. E. Ansell; Alice Pébay; Robyn H. Guymer; Aaron Y. Lee; Zhichao Wu
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Base editing of trinucleotide repeats that cause Huntington's disease and Friedreich's ataxia reduces somatic repeat expansions in patient cells and in mice
err2025-05-26
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errOAAI
errMatuszek, Zaneta; Arbab, Mandana; Kesavan, Maheswaran; Hsu, Alvin; Roy, Jennie C. L.; Zhao, Jing; Yu, Tian; Weisburd, Ben; Newby, Gregory A.; Doherty, Neil J.; Wu, Muzhou; Shibata, Shota; Cristian, Ana; Tao, Y. Allen; Fearnley, Liam G.; Bahlo, Melanie; Rehm, Heidi L.; Xie, Jun; Gao, Guangping; Mouro Pinto, Ricardo; Liu, David R.
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Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variants
err2025-05-22
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errOAAI
errSikta, Neblina; Gooley, Samuel; Green, Timothy E.; Hoeper, Olivia; Witkowski, Tom; Bennett, Caitlin; Francis, David; Reid, Joshua; Mao, Kevin; Awad, Mohammed; Roberts-Thomson, Samuel; Bulluss, Kristian; Clark, Jonathan; Scheffer, Ingrid E.; Perucca, Piero; Bennett, Mark F.; Bahlo, Melanie; Berkovic, Samuel F.; Hildebrand, Michael S.
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Psychoses of Epilepsy: Unravelling the Phenotypic and Genotypic Features
err2025-02-14
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errOAAI
errRayner, Genevieve; Honybun, Eliza; Bahlo, Melanie; Oliver, Karen L.; Scheffer, Ingrid E.
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Multi-omic spatial effects on high-resolution AI-derived retinal thickness
err2025-02-04
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errOAAI
errJackson, V. E.; Wu, Y.; Bonelli, R.; Owen, J. P.; Scott, L. W.; Farashi, S.; Kihara, Y.; Gantner, M. L.; Egan, C.; Williams, K. M.; Ansell, B. R. E.; Tufail, A.; Lee, A. Y.; Bahlo, M.
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Novel, complex configurations of the MARCHF6 repeat expansion associated with progressive myoclonic epilepsy and familial adult myoclonic epilepsy
err2025-01-01
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errOAAI
errBennett, Mark F.; Corbett, Mark A.; Kroes, Thessa; Canafoglia, Laura; Oliver, Karen L.; Cameron, Jillian M.; Sikta, Neblina; Munro, Jacob; Fearnley, Liam G.; Ibanez, Kristina; Tucci, Arianna; Sisodiya, Sanjay M.; Hildebrand, Michael S.; Scheffer, Ingrid E.; Courage, Carolina; Lehesjoki, Anna-Elina; Giuliano, Loretta; Didato, Giuseppe; Franceschetti, Silvana; Gecz, Jozef; Berkovic, Samuel F.; Bahlo, Melanie
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Drug repurposing candidates for amyotrophic lateral sclerosis using common and rare genetic variants
err2025-01-01
err1
PREAI
errGerring, Zachary F.; Bhalala, Oneil G.; Fearnley, Liam G.; Oikari, Lotta E.; White, Anthony R.; Derks, Eske M.; Watson, Rosie; Yassi, Nawaf; Bahlo, Melanie; Reay, William R.
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Peripheral immune cell abundance differences link blood mitochondrial DNA copy number and Parkinson's disease
err2024-11-14
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errOAAI
errWang, Longfei; Han, Jiru; Fearnley, Liam G.; Milton, Michael; Rafehi, Haloom; Reid, Joshua; Gerring, Zachary F.; Masaldan, Shashank; Lang, Tali; Speed, Terence P.; Bahlo, Melanie
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Inherited PURA Pathogenic Variant Associated With a Mild Neurodevelopmental Disorder
err2024-10-01
err1
errOAAI
errHildebrand, Michael S.; Braden, Ruth O.; Lauretta, Mariana L.; Kaspi, Antony; Leventer, Richard J.; Anderson, Melinda; Goel, Himanshu; Bahlo, Melanie; Scheffer, Ingrid E.; Amor, David J.; Janowski, Robert; Niessing, Dierk; Morgan, Angela T.
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LEVERAGING GENETIC PLEIOTROPY IN DRUG TARGET DISCOVERY FOR PSYCHIATRIC DISORDERS
err2024-10-01
err0
PREAI
errGerring, Zachary; Thorp, Jackson; Bahlo, Melanie; Derks, Eske
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Clinical, Radiological and Pathological Features of a Large American Cohort of Spinocerebellar Ataxia (SCA27B)
err2024-09-12
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errOAAI
errAbou Chaar, Widad; Eranki, Anirudh N.; Stevens, Hannah A.; Watson, Sonya L.; Wong, Darice Y.; Avila, Veronica S.; Delfeld, Megan; Gary, Alexander J.; Tawde, Sanjukta; Triebold, Malia; Cherchi, Marcello; Xie, Tao; Lockhart, Paul J.; Bahlo, Melanie; Pellerin, David; Dicaire, Marie-Josee; Danzi, Matt; Zuchner, Stephan; Brais, Bernard C.; Perlman, Susan; Burmeister, Margit; Paulson, Henry; Srinivasan, Sharan; Schut, Lawrence; Bower, Matthew; Bushara, Khalaf; Liao, Chuanhong; Shakkottai, Vikram G.; Collins, John; Clark, H. Brent; Das, Soma; Fogel, Brent L.; Gomez, Christopher M.
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Inflation of polygenic risk scores caused by sample overlap and relatedness: Examples of a major risk of bias
err2024-09-01
err2
PREAI
errEllis, Colin A.; Oliver, Karen L.; Harris, Rebekah, V; Ottman, Ruth; Scheffer, Ingrid E.; Mefford, Heather C.; Epstein, Michael P.; Berkovic, Samuel F.; Bahlo, Melanie
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