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The challenge of detecting epistasis (G x G interactions): Genetic Analysis Workshop 16.
An P, Mukherjee O, Chanda P, Yao L, Engelman CD, Huang CH, Zheng T, Kovac IP, Dubé MP, Liang X, Li J, de Andrade M, Culverhouse R, Malzahn D, Manning AK, Clarke GM, Jung J, Province MA. An P, et al. Among authors: mukherjee o. Genet Epidemiol. 2009;33 Suppl 1(0 1):S58-67. doi: 10.1002/gepi.20474. Genet Epidemiol. 2009. PMID: 19924703 Free PMC article.
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin.
Mukherjee O, Pastor P, Cairns NJ, Chakraverty S, Kauwe JS, Shears S, Behrens MI, Budde J, Hinrichs AL, Norton J, Levitch D, Taylor-Reinwald L, Gitcho M, Tu PH, Tenenholz Grinberg L, Liscic RM, Armendariz J, Morris JC, Goate AM. Mukherjee O, et al. Ann Neurol. 2006 Sep;60(3):314-22. doi: 10.1002/ana.20963. Ann Neurol. 2006. PMID: 16983685 Free PMC article.
Neuropathologic heterogeneity in HDDD1: a familial frontotemporal lobar degeneration with ubiquitin-positive inclusions and progranulin mutation.
Behrens MI, Mukherjee O, Tu PH, Liscic RM, Grinberg LT, Carter D, Paulsmeyer K, Taylor-Reinwald L, Gitcho M, Norton JB, Chakraverty S, Goate AM, Morris JC, Cairns NJ. Behrens MI, et al. Among authors: mukherjee o. Alzheimer Dis Assoc Disord. 2007 Jan-Mar;21(1):1-7. doi: 10.1097/WAD.0b013e31803083f2. Alzheimer Dis Assoc Disord. 2007. PMID: 17334266
Progranulin mutations and amyotrophic lateral sclerosis or amyotrophic lateral sclerosis-frontotemporal dementia phenotypes.
Schymick JC, Yang Y, Andersen PM, Vonsattel JP, Greenway M, Momeni P, Elder J, Chiò A, Restagno G, Robberecht W, Dahlberg C, Mukherjee O, Goate A, Graff-Radford N, Caselli RJ, Hutton M, Gass J, Cannon A, Rademakers R, Singleton AB, Hardiman O, Rothstein J, Hardy J, Traynor BJ. Schymick JC, et al. Among authors: mukherjee o. J Neurol Neurosurg Psychiatry. 2007 Jul;78(7):754-6. doi: 10.1136/jnnp.2006.109553. Epub 2007 Mar 19. J Neurol Neurosurg Psychiatry. 2007. PMID: 17371905 Free PMC article.
Evidence of linkage and association on 18p11.2 for psychosis.
Mukherjee O, Meera P, Ghosh S, Kubendran S, Kiran K, Manjunath KR, Subhash MN, Benegal V, Brahmachari SK, Majumder PP, Jain S. Mukherjee O, et al. Am J Med Genet B Neuropsychiatr Genet. 2006 Dec 5;141B(8):868-73. doi: 10.1002/ajmg.b.30363. Am J Med Genet B Neuropsychiatr Genet. 2006. PMID: 16941653
Effect of CLU and PICALM polymorphisms on AD risk: A study from south India.
Shankarappa BM, Kota LN, Purushottam M, Nagpal K, Mukherjee O, Viswanath B, Varghese M, Bharath S, Jain S. Shankarappa BM, et al. Among authors: mukherjee o. Asian J Psychiatr. 2017 Jun;27:7-11. doi: 10.1016/j.ajp.2016.12.017. Epub 2016 Dec 29. Asian J Psychiatr. 2017. PMID: 28558900
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