Edward M. Scolnick

Biochemistry, Genetics and Molecular BiologyAgricultural and Biological Sciences

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 12 papers. Top paper: “Rare coding variants in ten genes confer substantial risk for schizophrenia”.

Rare coding variants in ten genes confer substantial risk for schizophrenia

Nature(2022)10.1038/s41586-022-04556-w

N/A

7.2DataRank · unranked

900 citations

Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas +95 more

Biological insights from 108 schizophrenia-associated genetic loci

Nature(2014)10.1038/nature13595

N/A

1.3DataRank · unranked

8042 citations

Stephan Ripke, Aiden Corvin, Jesse R. Dixon, Kai-How Farh, Peter Holmans +284 more

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Nature(2011)10.1038/nature10251

N/A

1.2DataRank · unranked

2729 citations

Stephen Sawcer, Garrett Hellenthal, Matti Pirinen, Chris C. A. Spencer, Nikolaos A. Patsopoulos +241 more

Rare chromosomal deletions and duplications increase risk of schizophrenia

Nature(2008)10.1038/nature07239

N/A

1.1DataRank · unranked

1503 citations

Michael C O'Donovan, Catherine H. Wilson, Manfred Kayser, Pentti J. Tienari, Aiden Corvin +72 more

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

Nature Genetics(2016)10.1038/ng.3725

N/A

1.1DataRank · unranked

1129 citations

Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer +267 more

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

Cell Genomics(2023)10.1016/j.xgen.2023.100356

N/A

1.0DataRank · unranked

43 citations

Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Tushar Kamath, S.J. Burris +95 more

Validating therapeutic targets through human genetics

Nature Reviews Drug Discovery(2013)10.1038/nrd4051

N/A

0.995DataRank · unranked

758 citations

Edward M. Scolnick, David Altshuler, Robert M. Plenge

Analysis of High-Resolution HapMap of DTNBP1 (Dysbindin) Suggests No Consistency between Reported Common Variant Associations and Schizophrenia

The American Journal of Human Genetics(2006)10.1086/508942

N/A

0.719DataRank · unranked

120 citations

Derek W. Morris, Skye G. Waggoner, Coleen Damcott, Edward M. Scolnick, Jeremiah M. Scharf +1 more

Mammalian brain glycoproteins exhibit diminished glycan complexity compared to other tissues

Nature Communications(2022)10.1038/s41467-021-27781-9

N/A

0.705DataRank · unranked

109 citations

Maxence Noël, Sylvain Lehoux, Murat Çetinbaş, Ramnik J. Xavier, Ruslan I. Sadreyev +5 more

The schizophrenia-associated variant in SLC39A8 alters N-glycosylation in the mouse brain

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.12.22.424076

N/A

0.165DataRank · unranked

2 citations

Sarah Williams, Maxence Noël, Bo Yang, Alexandria K. D’Souza, Toru Nakata +10 more

Selective inhibition of glycogen synthase kinase 3α corrects pathophysiology in a mouse model of fragile X syndrome

Science Translational Medicine(2020)10.1126/scitranslmed.aam8572

N/A

0DataRank · unranked

61 citations

Laura J. Stoppel, Rebecca K. Senter, Michael C. Lewis, Arnold J. Heynen, David C. Stoppel +12 more

A polygenic burden of rare disruptive mutations in schizophrenia

UNC Libraries(2020)10.17615/carr-e613

N/A

0DataRank · unranked

0 citations

Sarah E. Bergen, Steven A. McCarroll, Eric S. Lander, Stacey B. Gabriel, Giulio Genovese +27 more