Mahdi Ghani

2000 -

ocupació: investigador

Sèrie

There is nothing here

Create a new serie

Treballs

There is nothing here

Create a new work

Articles 28

Date

Títol

Autors

2018-04-04

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease.

Robert A. Hegele, Ekaterina Rogaeva, Anthony Lang, Sandra Black, Lorne Zinman, Christine Sato, Mahdi Ghani, Mario Masellis, Morris Freedman, Adam D. McIntyre, Allison A Dilliott
2016-03-21

Mutation analysis of the MS4A and TREM gene clusters in a case-control Alzheimer's disease data set.

Mahdi Ghani, Peter Henry St George-Hyslop, Ekaterina Rogaeva, Bryan Traynor, Christine Sato, J Raphael Gibbs
2016-03-10

Novel GRN Mutations in Patients with Corticobasal Syndrome

Foad Taghdiri, Mahdi Ghani
2016-05-06

Genetic and epigenetic study of ALS-discordant identical twins with double mutations in SOD1 and ARHGEF28.

Mahdi Ghani, Ekaterina Rogaeva
2016-10-12

Characterizing familial corticobasal syndrome due to Alzheimer's disease pathology and PSEN1 mutations.

Mahdi Ghani, Peter Henry St George-Hyslop, Ekaterina Rogaeva, Sandra Black, Julia Keith, Mario Masellis, Morris Freedman
2016-06-13

Genetic Variations in ABCA7 Can Increase Secreted Levels of Amyloid-β40 and Amyloid-β42 Peptides and ABCA7 Transcription in Cell Culture Models.

Mahdi Ghani, Ekaterina Rogaeva
2015-09-14

Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals

Margaret A. Pericak-Vance, Ekaterina Rogaeva, Peter Henry St George-Hyslop, Nilüfer Ertekin-Taner, Chiao-Feng Lin, Gyungah Jun, Lindsay A. Farrer, Robert C. Green, Tatiana Foroud, Richard Mayeux, Christiane Reitz, David A Bennett, Walter A. Kukull, Jonathan L Haines, Joseph Buxbaum, Paul K. Crane, Philip L De Jager, Kathleen S. Hall, Oscar L Lopez, M. Ilyas Kamboh, Neill R Graff-Radford, Adam C Naj, Mark W Logue, Clinton Baldwin, Lisa J Barnes, Jennifer J Manly, Kathryn L. Lunetta, Alison Goate, Joseph H. Lee, Gerard D Schellenberg, Alzheimer's Disease Genetics Consortium, Christine Sato, Mahdi Ghani, Laura B Cantwell, Daniele Fallin, Goldie S Byrd, Badri Narayan Vardarajan, Ruchita A Rajbhandary, Otto Valladares, Towfique Raj, Patrick Griffiths, Thomas O Obisesan, Jill R Murrell
2015-02-01

Coding mutations in SORL1 and Alzheimer disease

Mahdi Ghani, Peter Henry St George-Hyslop, Richard Mayeux, Christiane Reitz, Ekaterina Rogaeva, Joseph H. Lee, Christopher Bohm, Yalun Zhang, Dolly Reyes-Dumeyer
2015-06-23

Rare coding mutations identified by sequencing of Alzheimer disease genome-wide association studies loci

Mahdi Ghani, Peter Henry St George-Hyslop, Richard Mayeux, Christiane Reitz, Ekaterina Rogaeva, Joseph H. Lee, Christine Sato, Dolly Reyes-Dumeyer, Sandra María Barral Rodríguez
2015-11-06

Mutation analysis of CHCHD2 in Canadian patients with familial Parkinson's disease

Ekaterina Rogaeva, Anthony Lang, Christine Sato, Danielle Moreno, Mahdi Ghani
2015-03-31

Mutation analysis of CHCHD10 in different neurodegenerative diseases

Daniela Galimberti, Mahdi Ghani, Elisa Rubino, Benedetta Nacmias, Sandro Sorbi, Peter Henry St George-Hyslop, Anthony Lang, Ekaterina Rogaeva, Susan H Fox, Bryan Traynor, Lorne Zinman, Amalia Bruni, Innocenzo Rainero, Lorenzo Pinessi, Christine Sato, Ezequiel I Surace, Danielle Moreno, Julia Keith, Sabrina A M Curcio, Raffaele Maletta
2015-11-02

MTHFSD and DDX58 are novel RNA-binding proteins abnormally regulated in amyotrophic lateral sclerosis.

Mahdi Ghani, Ekaterina Rogaeva, Jean-Pierre Julien
2014-09-10

Identical twins with the C9orf72 repeat expansion are discordant for ALS

Marka van Blitterswijk, Mahdi Ghani, Yana Yunusova, Ekaterina Rogaeva, Rosa Rademakers, Andrew Singleton
2014-08-01

Mutation analysis of patients with neurodegenerative disorders using NeuroX array

Mahdi Ghani, Benedetta Nacmias, Sandro Sorbi, Peter Henry St George-Hyslop, Anthony Lang, Ekaterina Rogaeva, Andrew Singleton, Lorne Zinman, Christine Sato, Maria Carmela Tartaglia, Ezequiel I Surace, Danielle Moreno, Andrea Tedde, Valentina Bessi
2014-11-13

Inbreeding among Caribbean Hispanics from the Dominican Republic and its effects on risk of Alzheimer disease

Mahdi Ghani, Joseph H. Lee, Peter Henry St George-Hyslop, Christiane Reitz, Ekaterina Rogaeva, Richard Mayeux
2013-10-01

Evidence of recessive Alzheimer disease loci in a Caribbean Hispanic data set: genome-wide survey of runs of homozygosity

Mahdi Ghani, Peter Henry St George-Hyslop, Richard Mayeux, Christiane Reitz, Ekaterina Rogaeva, Joseph H. Lee, Christine Sato, Danielle Moreno
2013-02-15

Role of p73 in Alzheimer disease: lack of association in mouse models or in human cohorts

Kunie Ando, Mahdi Ghani, Mark W Logue, Clinton Baldwin, Jean-Pierre Brion, Peter Henry St George-Hyslop, Lindsay A. Farrer, Fadel Tissir, Richard Mayeux, Ekaterina Rogaeva, Joseph H. Lee
2013-05-14

Independent and epistatic effects of variants in VPS10-d receptors on Alzheimer disease risk and processing of the amyloid precursor protein (APP)

Mahdi Ghani, Richard Mayeux, Christiane Reitz, Ekaterina Rogaeva, Jonathan L Haines, Alzheimer's Disease Genetics Consortium (ADGC), Peter Henry St George-Hyslop, Lindsay A. Farrer
2013-05-23

Hypermethylation of the CpG island near the G4C2 repeat in ALS with a C9orf72 expansion

Mahdi Ghani, Yonglan Zheng, Ekaterina Rogaeva
2012-01

Genome-wide survey of large rare copy number variants in Alzheimer's disease among Caribbean hispanics

Ekaterina Rogaeva, Peter Henry St George-Hyslop, Mahdi Ghani, Dalila Pinto, Stephen W. Scherer, Richard Mayeux, Joseph H. Lee, Christine Sato, Danielle Moreno
2012-07-20

Epidemiology and genetics of frontotemporal dementia: a door-to-door survey in southern Italy

Nicoletta Smirne, Rosanna Colao, Chiara Cupidi, Mahdi Ghani, Peter Henry St George-Hyslop, Maria Anfossi, Gianfranco Puccio, Livia Bernardi, Raffaele Maletta
2012-12-01

Investigation of c9orf72 in 4 neurodegenerative disorders

Mahdi Ghani, Jordi Clarimón, Daniela Galimberti, Peter Henry St George-Hyslop, Sandra Black, Anthony Lang, Karen E Morrison, Richard Mayeux, Ekaterina Rogaeva, Connie Fernández-Cid Marras, Lili-Naz Hazrati, Danielle Moreno, Christine Sato, Mario Masellis, Lorne Zinman, Mercè Boada, Amalia Bruni, Innocenzo Rainero, Lorenzo Pinessi, Janice L Robertson, Rosanna Colao, Gianfranco Puccio, Raffaele Maletta
2012-12-11

Segmental duplications in genome-wide significant loci and housekeeping genes; warning for GAPDH and ACTB.

Mahdi Ghani, Ekaterina Rogaeva
2012-07-21

Genetic association of CR1 with Alzheimer's disease: a tentative disease mechanism.

Nathalie Brouwers, Mahdi Ghani, Peter Henry St George-Hyslop, Christine Van Broeckhoven, Ekaterina Rogaeva, Christine Sato, Lili-Naz Hazrati
2012-09

Fcγ Receptor Polymorphisms Do Not Predict Response to Intravenous Immunoglobulin in Myasthenia Gravis

Mahdi Ghani, Carolina Barnett, Peter Henry St George-Hyslop, Ekaterina Rogaeva, Vera Bril
2011-09-01

Misregulation of mitotic chromosome segregation in a new type of autosomal recessive primary microcephaly

Mahdi Ghani, Peter Robinson, Ioannis Gavvovidis, Peter Krawitz, Luitgard Graul-Neumann, Heidemarie Neitzel, Detlev Schindler, Marc Trimborn, Andreas Busche, Nadine Sternberg, Juan Alberto Marchal Ortega
2010

Establishment of a mouse model with misregulated chromosome condensation due to defective Mcph1 function

Hans-Hilger Ropers, Ioannis Gavvovidis, Mahdi Ghani, Masoud Garshasbi, Heidemarie Neitzel, Detlev Schindler, Marc Trimborn, Véronique Dutrannoy, Andreas Busche
2010-10-26

A clinical and molecular genetic study of 112 Iranian families with primary microcephaly

Mahdi Ghani, Hossein Najmabadi, Masoumeh Falah, Farkhondeh Behjati, Kimia Kahrizi

Human - wd:Q41935071

Welcome to Inventaire

la biblioteca dels teus amics i comunitats

saber més