🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Corrine Smolen

Pennsylvania State University

ORCID: 0000-0001-5951-5365
Biochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 8 papers. Top paper: “Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletion”.

Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletion

Genome Medicine(2021)10.1186/s13073-021-00982-z
N/A
0.385DataRank · unranked
12 citations

Anastasia Tyryshkina, Lucilla Pizzo, Corrine Smolen, Maitreya Das, Emily Huber +3 more

Genetic modifiers and ascertainment drive variable expressivity of complex disorders

medRxiv(2024)10.1101/2024.08.27.24312158
N/A
0.269DataRank · unranked
5 citations

Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Deepro Banerjee, Matthew T. Oetjens +65 more

Generation and characterization of Ccdc28b mutant mice links the Bardet-Biedl associated gene with social behavioral phenotypes

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.10.21.465251
N/A
0DataRank · unranked
0 citations

Sofía Niño, Sabrina Pose, Magdalena Cárdenas-Rodríguez, Corrine Smolen, Mariana Bresque +11 more

Scn8a Antisense Oligonucleotide Is Protective in Mouse Models of SCN8A Encephalopathy and Dravet Syndrome

Annals of Neurology(2020)10.1002/ana.25676
N/A
0DataRank · unranked
141 citations

Paymaan Jafar‐Nejad, Sophie F. Hill, Lucas D. Huffman, Corrine Smolen, Jacy L. Wagnon +9 more

Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.015
N/A
0DataRank · unranked
40 citations

Matthew Jensen, Lisa Dyer, Lucilla Pizzo, Anastasia Tyryshkina, Deepro Banerjee +38 more

Assortative mating and parental genetic relatedness drive the pathogenicity of variably expressive variants

medRxiv(2023)10.1101/2023.05.18.23290169
N/A
0DataRank · unranked
5 citations

Matthew Jensen, Lisa Dyer, Lucilla Pizzo, Anastasia Tyryshkina, Deepro Banerjee +38 more

The gene dose makes the disease

Cell(2022)10.1016/j.cell.2022.07.005
N/A
0DataRank · unranked
5 citations

Santhosh Girirajan, Corrine Smolen

Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12.1 deletion

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.03.06.434203
N/A
0DataRank · unranked
0 citations

Anastasia Tyryshkina, Lucilla Pizzo, Corrine Smolen, Maitreya Das, Emily Huber +3 more