Paper Search Results
Home Page
More Results
Recommendations from ProNE (based on Citation Graph)
AuthorId: 3253547
Limit: 10
Sort by: score
Embedding: s2_recommendations
IP address: 3.144.31.17
Freq flyer: False
authorId(s): 3253547
Author(s): D. Geschwind
score
citationCount
Paper
Authors
year
More like this
Compare & Contrast
ProNE-s
SciNCL
Specter
GNN
4435
Expanded GGGGCC Hexanucleotide Repeat in Noncoding Region of C9ORF72 Causes Chromosome 9p-Linked FTD and ALS
M. Dejesus‐Hernandez
,
I. Mackenzie
, ...,
R. Rademakers
2011
Similar to this
Compare & Contrast
2378
An anatomically comprehensive atlas of the adult human brain transcriptome
M. Hawrylycz
,
E. Lein
, ...,
Allan R. Jones
2012
Similar to this
Compare & Contrast
2106
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. H. Lee
,
S. Ripke
, ...,
N. Wray
2013
Similar to this
Compare & Contrast
1969
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
Stephan J Sanders
,
M. Murtha
, ...,
M. State
2012
Similar to this
Compare & Contrast
1905
Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
B. Kunkle
,
B. Grenier‐Boley
, ...,
M. Pericak-Vance
2019
Similar to this
Compare & Contrast
1569
Identification of common genetic risk variants for autism spectrum disorder
J. Grove
,
S. Ripke
, ...,
A. Børglum
2019
Similar to this
Compare & Contrast
1560
Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder
D. Demontis
,
R. Walters
, ...,
B. Neale
2018
Similar to this
Compare & Contrast
1505
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Satterstrom
,
J. Kosmicki
, ...,
R. Walters
2019
Similar to this
Compare & Contrast
1275
Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection
A. Pardiñas
,
P. Holmans
, ...,
J. Walters
2018
Similar to this
Compare & Contrast
1254
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan J Sanders
,
A. Ercan-Sencicek
, ...,
M. State
2011
Similar to this
Compare & Contrast
Help
Bulk Download
GitHub
Final Report (YouTube)
JSALT-2023
Contact us (by email)
BETA Version