متابعة
Hannah A Pliner
Hannah A Pliner
بريد إلكتروني تم التحقق منه على uw.edu
عنوان
عدد مرات الاقتباسات
عدد مرات الاقتباسات
السنة
Reversed graph embedding resolves complex single-cell trajectories
X Qiu, Q Mao, Y Tang, L Wang, R Chawla, HA Pliner, C Trapnell
Nature methods 14 (10), 979-982, 2017
29122017
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
Nature genetics 46 (9), 989-993, 2014
20202014
Multiplex single-cell profiling of chromatin accessibility by combinatorial cellular indexing
DA Cusanovich, R Daza, A Adey, HA Pliner, L Christiansen, ...
Science 348 (6237), 910-914, 2015
11602015
Joint profiling of chromatin accessibility and gene expression in thousands of single cells
J Cao, DA Cusanovich, V Ramani, D Aghamirzaie, HA Pliner, AJ Hill, ...
Science 361 (6409), 1380-1385, 2018
7432018
A single-cell atlas of in vivo mammalian chromatin accessibility
DA Cusanovich, AJ Hill, D Aghamirzaie, RM Daza, HA Pliner, JB Berletch, ...
Cell 174 (5), 1309-1324. e18, 2018
6692018
Cicero predicts cis-regulatory DNA interactions from single-cell chromatin accessibility data
HA Pliner, JS Packer, JL McFaline-Figueroa, DA Cusanovich, RM Daza, ...
Molecular cell 71 (5), 858-871. e8, 2018
6002018
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5762018
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ...
Nature neuroscience 17 (5), 664-666, 2014
5142014
A human cell atlas of fetal gene expression
J Cao, DR O’day, HA Pliner, PD Kingsley, M Deng, RM Daza, MA Zager, ...
Science 370 (6518), eaba7721, 2020
4912020
Supervised classification enables rapid annotation of cell atlases
HA Pliner, J Shendure, C Trapnell
Nature methods 16 (10), 983-986, 2019
3802019
The cis-regulatory dynamics of embryonic development at single-cell resolution
DA Cusanovich, JP Reddington, DA Garfield, RM Daza, D Aghamirzaie, ...
Nature 555 (7697), 538-542, 2018
3382018
A human cell atlas of fetal chromatin accessibility
S Domcke, AJ Hill, RM Daza, J Cao, DR O’Day, HA Pliner, KA Aldinger, ...
Science 370 (6518), eaba7612, 2020
2832020
Massively multiplex chemical transcriptomics at single-cell resolution
SR Srivatsan, JL McFaline-Figueroa, V Ramani, L Saunders, J Cao, ...
Science 367 (6473), 45-51, 2020
2392020
A genome-wide association study of myasthenia gravis
AE Renton, HA Pliner, C Provenzano, A Evoli, R Ricciardi, MA Nalls, ...
JAMA neurology 72 (4), 396-404, 2015
1762015
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis
S Bandres‐Ciga, AJ Noyce, G Hemani, A Nicolas, A Calvo, G Mora, ...
Annals of neurology 85 (4), 470-481, 2019
1602019
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
MA Nalls, J Bras, DG Hernandez, MF Keller, E Majounie, AE Renton, ...
Neurobiology of aging 36 (3), 1605. e7-1605. e12, 2015
114*2015
Genetic architecture of ALS in Sardinia
G Borghero, M Pugliatti, F Marrosu, MG Marrosu, MR Murru, G Floris, ...
Neurobiology of aging 35 (12), 2882. e7-2882. e12, 2014
702014
The accessible chromatin landscape of the murine hippocampus at single-cell resolution
JR Sinnamon, KA Torkenczy, MW Linhoff, SA Vitak, RM Mulqueen, ...
Genome Research 29 (5), 857-869, 2019
642019
Parkinson’s Study Group (PSG) Parkinson’s Research: The Organized GENetics Initiative (PROGENI); 23andMe
MA Nalls, N Pankratz, CM Lill, CB Do, DG Hernandez, M Saad, ...
GenePD 46 (9), 989-93, 2014
582014
Association of variants in the SPTLC1 gene with juvenile amyotrophic lateral sclerosis
JO Johnson, R Chia, DE Miller, R Li, R Kumaran, Y Abramzon, ...
JAMA neurology 78 (10), 1236-1248, 2021
542021
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مقالات 1–20