X
Search Filters
Format Format
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
index medicus (17) 17
humans (12) 12
article (9) 9
genetics (8) 8
genomes (8) 8
neurosciences (8) 8
amyotrophic lateral sclerosis (6) 6
analysis (6) 6
genes (6) 6
research (6) 6
amyotrophic lateral sclerosis - genetics (5) 5
amyotrophic-lateral-sclerosis (5) 5
chromatin (5) 5
female (5) 5
gene expression (5) 5
genetic aspects (5) 5
genetic research (5) 5
genotype (5) 5
male (5) 5
mutation (5) 5
animals (4) 4
biochemistry & molecular biology (4) 4
genome-wide association study (4) 4
genomics (4) 4
geriatrics & gerontology (4) 4
gwas (4) 4
internal medicine (4) 4
multidisciplinary sciences (4) 4
neurology (4) 4
transcription factors (4) 4
accessibility (3) 3
aged (3) 3
als (3) 3
atac-seq (3) 3
c9orf72 protein (3) 3
cells (3) 3
clinical neurology (3) 3
combinatorial analysis (3) 3
expression (3) 3
genetic predisposition to disease - genetics (3) 3
genetics & heredity (3) 3
genome-wide association (3) 3
methods (3) 3
middle aged (3) 3
proteins - genetics (3) 3
read alignment (3) 3
risk factors (3) 3
single-cell analysis - methods (3) 3
age of onset (2) 2
algorithms (2) 2
alleles (2) 2
alzheimers-disease (2) 2
amyotrophic lateral sclerosis - pathology (2) 2
bioinformatics (2) 2
case-control studies (2) 2
cell biology (2) 2
cell fate (2) 2
chromatin - metabolism (2) 2
chromatin accessibility (2) 2
common variants (2) 2
developmental biology (2) 2
disease (2) 2
dna methylation (2) 2
dna repeat expansion (2) 2
dna-damage (2) 2
embryogenesis (2) 2
embryonic development (2) 2
embryonic growth stage (2) 2
epigenesis, genetic (2) 2
frontotemporal dementia (2) 2
frontotemporal dementia - genetics (2) 2
gcta (2) 2
gene expression regulation (2) 2
gene regulation (2) 2
gene-expression (2) 2
genetic association studies (2) 2
genetic predisposition to disease (2) 2
genetic transcription (2) 2
genome (2) 2
genome-wide association study - methods (2) 2
greece (2) 2
heart (2) 2
hek293 cells (2) 2
heritability (2) 2
hexanucleotide repeat (2) 2
human genome (2) 2
identification (2) 2
imputation (2) 2
kidneys (2) 2
landscapes (2) 2
meta-analysis (2) 2
mice (2) 2
mutations (2) 2
parkinson disease - genetics (2) 2
parkinson's disease (2) 2
parkinsons-disease (2) 2
proteins (2) 2
risk (2) 2
risk profiles (2) 2
sequencing data (2) 2
more...
Language Language
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


Nature Methods, ISSN 1548-7091, 10/2017, Volume 14, Issue 10, pp. 979 - 982
Journal Article
Science, ISSN 0036-8075, 05/2015, Volume 348, Issue 6237, pp. 910 - 914
Technical advances have enabled the collection of genome and transcriptome data sets with single-cell resolution. However, single-cell characterization of the... 
IN-VITRO | HUMAN GENOME | RNA-SEQ | MULTIDISCIPLINARY SCIENCES | CONTIGUITY | FATE | EXPRESSION | TRANSPOSITION | HL-60 Cells | Chromatin - metabolism | Single-Cell Analysis - methods | Epigenesis, Genetic | Humans | HEK293 Cells | Chromatin | Research | Analysis | Cells | Indexing | Cellular biology | Tissue | Index Medicus | Multiplexing | Cellular | Landscapes | Accessibility | Strategy | Culture | Combinatorial analysis
Journal Article
GENOME RESEARCH, ISSN 1088-9051, 05/2019, Volume 29, Issue 5, pp. 857 - 869
Here we present a comprehensive map of the accessible chromatin landscape of the mouse hippocampus at single-cell resolution. Substantial advances of this work... 
SYSTEM | MARKER | BIOCHEMISTRY & MOLECULAR BIOLOGY | TRANSCRIPTION | ELECTROPHYSIOLOGY | MEMORY | GENOMES | CORTEX | BIOTECHNOLOGY & APPLIED MICROBIOLOGY | GENETICS & HEREDITY | NEURONS | DIVERSITY | EXPRESSION
Journal Article
Journal Article
by Johnson, Janel O and Pioro, Erik P and Boehringer, Ashley and Chia, Ruth and Feit, Howard and Renton, Alan E and Pliner, Hannah A and Abramzon, Yevgeniya and Marangi, Giuseppe and Winborn, Brett J and Gibbs, J. Raphael and Nalls, Michael A and Morgan, Sarah and Shoai, Maryam and Hardy, John and Pittman, Alan and Orrell, Richard W and Malaspina, Andrea and Sidle, Katie C and Fratta, Pietro and Harms, Matthew B and Baloh, Robert H and Pestronk, Alan and Weihl, Conrad C and Rogaeva, Ekaterina and Zinman, Lorne and Drory, Vivian E and Borghero, Giuseppe and Mora, Gabriele and Calvo, Andrea and Rothstein, Jeffrey D and Drepper, Carsten and Sendtner, Michael and Singleton, Andrew B and Taylor, J Paul and Cookson, Mark R and Restagno, Gabriella and Sabatelli, Mario and Bowser, Robert and Chio`, Adriano and Traynor, Bryan J and Moglia, Cristina and Cammarosano, Stefania and Canosa, Antonio and Gallo, Sara and Brunetti, Maura and Ossola, Irene and Marinou, Kalliopi and Papetti, Laura and Pisano, Fabrizio and Pinter, Giuseppe Lauria and Conte, Amelia and Luigetti, Marco and Zollino, Marcella and Lattante, Serena and Marangi, Giuseppe and la Bella, Vincenzo and Spataro, Rossella and Colletti, Tiziana and Battistini, Stefania and Ricci, Claudia and Caponnetto, Claudia and Mancardi, Gianluigi and Mandich, Paola and Salvi, Fabrizio and Bartolomei, Ilaria and Mandrioli, Jessica and Sola, Patrizia and Lunetta, Christian and Penco, Silvana and Monsurrò, Maria Rosaria and Conforti, Francesca Luisa and Tedeschi, Gioacchino and Gambardella, Antonio and Quattrone, Aldo and Volanti, Paolo and Floris, Gianluca and Cannas, Antonino and Piras, Valeria and Marrosu, Francesco and Marrosu, Maria Giovanna and Murru, Maria Rita and Pugliatti, Maura and Parish, Leslie D and Sotgiu, Alessandra and Solinas, Giuliana and Ulgheri, Lucia and Ticca, Anna and Simone, Isabella and Logroscino, Giancarlo and Pirisi, Angelo and ITALSGEN
Nature Neuroscience, ISSN 1097-6256, 2014, Volume 17, Issue 5, pp. 664 - 666
Journal Article
Journal Article
by Nicolas, Aude and Kenna, Kevin P and Kenna, Aoife and Kenna, Kevin and Kenna, Brendan J and Renton, Alan E and Ticozzi, Nicola and Faghri, Faraz and Chia, Ruth and Dominov, Janice A and Nalls, Mike A and Keagle, Pamela and Rivera, Alberto M and van Rheenen, Wouter and Murphy, Natalie A and van Vugt, Joke and van Vugt, Joke J.F.A and Geiger, Joshua T and Van der Spek, Rick A and Pliner, Hannah A and Shankaracharya and Smith, Bradley N and Marangi, Giuseppe and Topp, Simon D and Abramzon, Yevgeniya and Gkazi, Athina Soragia and Eicher, John D and Logullo, Francesco O and Simone, Isabella and Simone, Isabella L and Logroscino, Giancarlo and Salvi, Fabrizio and Bartolomei, Ilaria and Borghero, Giuseppe and Murru, Maria Rita and Costantino, Emanuela and Pani, Carla and Puddu, Roberta and Caredda, Carla and Piras, Valeria and Tranquilli, Stefania and Cuccu, Stefania and Corongiu, Daniela and Melis, Maurizio and Milia, Antonio and Marrosu, Francesco and Marrosu, Maria Giovanna and Floris, Gianluca and Cannas, Antonino and Capasso, Margherita and Caponnetto, Claudia and Mancardi, Gianluigi and Origone, Paola and Mandich, Paola and Conforti, Francesca L and Cavallaro, Sebastiano and Mora, Gabriele and Mora, Jesús S and Marinou, Kalliopi and Sideri, Riccardo and Penco, Silvana and Mosca, Lorena and Lunetta, Christian and Pinter, Giuseppe Lauria and Corbo, Massimo and Riva, Nilo and Carrera, Paola and Volanti, Paolo and Mandrioli, Jessica and Fini, Nicola and Fasano, Antonio and Tremolizzo, Lucio and Arosio, Alessandro and Ferrarese, Carlo and Trojsi, Francesca and Tedeschi, Gioacchino and Monsurrò, Maria Rosaria and Piccirillo, Giovanni and Femiano, Cinzia and Ticca, Anna and Ortu, Enzo and La Bella, Vincenzo and Spataro, Rossella and Colletti, Tiziana and Sabatelli, Mario and Zollino, Marcella and Conte, Amelia and Luigetti, Marco and Lattante, Serena and Santarelli, Marialuisa and Petrucci, Antonio and Pugliatti, Maura and Pirisi, Angelo and Parish, Leslie D and Occhineri, Patrizia and Giannini, Fabio and Battistini, Stefania and Ricci, Claudia and Benigni, Michele and Cau, Tea B and ... and Genomic Translation ALS Care GTAC and ALS Sequencing Consortium and Clinical Res ALS Related Disorders and NYGC ALS Consortium and ITALSGEN Consortium and SLAGEN Consortium and French ALS Consortium and Project MinE ALS Sequencing Consor and Answer ALS Fdn and Project MinE ALS Sequencing Consortium and Genomic Translation for ALS Care (GTAC) Consortium and Answer ALS Foundation and Clinical Research in ALS and Related Disorders for Therapeutic Development (CReATe) Consortium and Medicinska fakulteten and Institutionen för farmakologi och klinisk neurovetenskap and Umeå universitet
Neuron, ISSN 0896-6273, 03/2018, Volume 97, Issue 6, pp. 1268 - 1283.e6
Journal Article
Acta Neuropathologica, ISSN 0001-6322, 3/2014, Volume 127, Issue 3, pp. 391 - 396
Journal Article