STÖGER, REINHARD, WILLIAMS, PAULA, SHEPHARD, FREYA and CHAKRABARTI, LISA, 2017. Elevated 5hmC levels characterize DNA of the cerebellum in Parkinson's disease npj Parkinson's Disease. 3(1), 6 POLLARD, AMELIA K, ORTORI, CATHARINE A, STOGER, REINHARD, BARRETT, DAVID A and CHAKRABARTI, LISA, 2017. Mouse mitochondrial lipid composition is defined by age in brain and muscle. Aging. SHEPHARD, FREYA, GREVILLE-HEYGATE, OLIVER, LIDDELL, SUSAN, EMES, RICHARD and CHAKRABARTI, LISA, 2016. Analysis of mitochondrial haemoglobin in Parkinson's disease brain Mitochondrion. 29, 45-52 SHEPHARD F, GREVILLE-HEYGATE O, MARSH O, ANDERSON S and CHAKRABARTI L, 2014. A mitochondrial location for haemoglobins--dynamic distribution in ageing and Parkinson's disease. Mitochondrion. 14(1), 64-72 LATHROP, M.J., CHAKRABARTI, L., ENG, J., RHODES, C.H., LUTZ, T., NIETO, A., LIGGITT, H.D., WARNER, S., FIELDS, J., STÖGER, R. and FIERING, S., 2010. Deletion of the Chd6 exon 12 affects motor coordination Mammalian Genome. 21(3-4), 130-142 CHAKRABARTI, L., ZAHRA, R., JACKSON, S.M., KAZEMI-ESFARJANI, P., SOPHER, B.L., MASON, A.G., TONEFF, T., RYU, S., SHAFFER, S., KANSY, J.W., ENG, J., MERRIHEW, G., MACCROSS, M.J., MURPHY, A., GOODLETT, D.R. and HOOK, V., 2010. Mitochondrial dysfunction in NnaD mutant flies and Purkinje cell degeneration mice reveals a role for Nna proteins in neuronal bioenergetics Neuron. 66(6), 835-847 CHAKRABARTI, L., ENG, J., IVANOV, N., GARDEN, G.A. and LA SPADA, A.R., 2009. Autophagy activation and enhanced mitophagy characterize the Purkinje cells of pcd mice prior to neuronal death. Molecular Brain. 2(1), 24 CHAKRABARTI, L., ENG, J., MARTINEZ, R.A., JACKSON, S., HUANG, J., POSSIN, D.E., SOPHER, B.L. and LA SPADA, A.R., 2008. The zinc-binding domain of Nna1 is required to prevent retinal photoreceptor loss and cerebellar ataxia in Purkinje cell degeneration (pcd) mice Vision Research. 48(19), 1999-2005 CHAKRABARTI, LISA, NEAL, JAMES T, MILES, MICHAEL, MARTINEZ, REFUGIO A, SMITH, ANNETTE C, SOPHER, BRYCE L and LA SPADA, ALBERT R, 2006. The Purkinje cell degeneration 5J mutation is a single amino acid insertion that destabilizes Nna1 protein. Mammalian genome : official journal of the International Mammalian Genome Society. 17(2), 103-10
SKIBINSKI, GAIA, PARKINSON, NICHOLAS J, BROWN, JEREMY M, CHAKRABARTI, LISA, LLOYD, SARAH L, HUMMERICH, HOLGER, NIELSEN, JØRGEN E, HODGES, JOHN R, SPILLANTINI, MARIA GRAZIA, THUSGAARD, TOVE and BRAND, 2005. Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia. Nature genetics. 37(8), 806-8
BROWN, JERRY, GYDESEN, SUSANNE, JOHANNSEN, PETER, GADE, ANDERS, SKIBINSKI, GAIA, CHAKRABARTI, LISA, BRUN, ARNE, SPILLANTINI, MARIA, YANCOPOULOU, DESPINA, THUSGAARD, TOVE, SORENSEN, ASGER and FISHER, ELIZ, 2004. Frontotemporal dementia linked to chromosome 3. Dementia and geriatric cognitive disorders. 17(4), 274-6
YANCOPOULOU, DESPINA, CROWTHER, R ANTHONY, CHAKRABARTI, LISA, GYDESEN, SUSANNE, BROWN, JEREMY M and SPILLANTINI, MARIA GRAZIA, 2003. Tau protein in frontotemporal dementia linked to chromosome 3 (FTD-3). Journal of neuropathology and experimental neurology. 62(8), 878-82
GYDESEN, S, BROWN, J M, BRUN, A, CHAKRABARTI, L, GADE, A, JOHANNSEN, P, ROSSOR, M, THUSGAARD, T, GROVE, A, YANCOPOULOU, D, SPILLANTINI, M G, FISHER, E M C, COLLINGE, J and SORENSEN, S A, 2002. Chromosome 3 linked frontotemporal dementia (FTD-3). Neurology. 59(10), 1585-94 PETERS, M A, JARVIK, G P, JANER, M, CHAKRABARTI, L, KOLB, S, GOODE, E L, GIBBS, M, DUBOIS, C C, SCHUSTER, E F, HOOD, L, OSTRANDER, E A and STANFORD, J L, 2001. Genetic linkage analysis of prostate cancer families to Xq27-28. Human heredity. 51(1-2), 107-13
GOODE, E L, STANFORD, J L, CHAKRABARTI, L, GIBBS, M, KOLB, S, MCINDOE, R A, BUCKLEY, V A, SCHUSTER, E F, NEAL, C L, MILLER, E L, BRANDZEL, S, HOOD, L, OSTRANDER, E A and JARVIK, G P, 2000. Linkage analysis of 150 high-risk prostate cancer families at 1q24-25. Genetic epidemiology. 18(3), 251-75 GIBBS, M, STANFORD, J L, JARVIK, G P, JANER, M, BADZIOCH, M, PETERS, M A, GOODE, E L, KOLB, S, CHAKRABARTI, L, SHOOK, M, BASOM, R, OSTRANDER, E A and HOOD, L, 2000. A genomic scan of families with prostate cancer identifies multiple regions of interest. American journal of human genetics. 67(1), 100-9 GIBBS, M, STANFORD, J L, MCINDOE, R A, JARVIK, G P, KOLB, S, GOODE, E L, CHAKRABARTI, L, SCHUSTER, E F, BUCKLEY, V A, MILLER, E L, BRANDZEL, S, LI, S, HOOD, L and OSTRANDER, E A, 1999. Evidence for a rare prostate cancer-susceptibility locus at chromosome 1p36. American journal of human genetics. 64(3), 776-87
PARMANTIER, E, LYNN, B, LAWSON, D, TURMAINE, M, NAMINI, S S, CHAKRABARTI, L, MCMAHON, A P, JESSEN, K R and MIRSKY, R, 1999. Schwann cell-derived Desert hedgehog controls the development of peripheral nerve sheaths. Neuron. 23(4), 713-24 GIBBS, M, CHAKRABARTI, L, STANFORD, J L, GOODE, E L, KOLB, S, SCHUSTER, E F, BUCKLEY, V A, SHOOK, M, HOOD, L, JARVIK, G P and OSTRANDER, E A, 1999. Analysis of chromosome 1q42.2-43 in 152 families with high risk of prostate cancer. American journal of human genetics. 64(4), 1087-95 CHAKRABARTI, L, BRISTULF, J, FOSS, G S and DAVIES, K E, 1998. Expression of the murine homologue of FMR2 in mouse brain and during development. Human molecular genetics. 7(3), 441-8 CHAKRABARTI, L and DAVIES, K E, 1997. Fragile X syndrome. Current opinion in neurology. 10(2), 142-7
RITCHIE, R J, CHAKRABARTI, L, KNIGHT, S J, HARDING, R M and DAVIES, K E, 1997. Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28. American journal of medical genetics. 73(4), 463-9
KNIGHT, S J, RITCHIE, R J, CHAKRABARTI, L, CROSS, G, TAYLOR, G R, MUELLER, R F, HURST, J, PATERSON, J, YATES, J R, DOW, D J and DAVIES, K E, 1996. A study of FRAXE in mentally retarded individuals referred for fragile X syndrome (FRAXA) testing in the United Kingdom. American journal of human genetics. 58(5), 906-13
CHAKRABARTI, L, KNIGHT, S J, FLANNERY, A V and DAVIES, K E, 1996. A candidate gene for mild mental handicap at the FRAXE fragile site. Human molecular genetics. 5(2), 275-82