Tarjinder Singh

Also affiliated with Columbia University Irving Medical Center, New York Genome Center, Columbia University

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 17 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

Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia

Nature Genetics(2022)10.1038/s41588-022-01034-x

N/A

3.5DataRank · unranked

214 citations

Daniel P. Howrigan, Sinéad B. Chapman, Rolf Adolfsson, Nick Bass, Douglas Blackwood +42 more

The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia

Nature Communications(2022)10.1038/s41467-022-31436-8

N/A

1.4DataRank · unranked

61 citations

Olli Pietiläinen, Mykyta Artomov, Matthew Tegtmeyer, Vera Valakh, Leevi Lehtonen +40 more

Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals

Nature Communications(2023)10.1038/s41467-023-39539-6

N/A

1.2DataRank · unranked

56 citations

David Lewis‐Smith, Ryan L. Collins, Lisa‐Marie Niestroj, Shridhar Parthasarathy, Julie Xian +94 more

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Nature Genetics(2017)10.1038/ng.3903

N/A

0.826DataRank · unranked

246 citations

David M. Hougaard, Mandy Johnstone, Nicholas Bass, Jaana Suvisaari, Minna Torniainen +21 more

Autism spectrum disorder and attention deficit hyperactivity disorder have a similar burden of rare protein-truncating variants

Nature Neuroscience(2019)10.1038/s41593-019-0527-8

N/A

0.815DataRank · unranked

228 citations

F. Kyle Satterstrom, Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis +17 more

The impact of rare protein coding genetic variation on adult cognitive function

Nature Genetics(2023)10.1038/s41588-023-01398-8

N/A

0.628DataRank · unranked

65 citations

Ruoyu Tian, Tian Ge, Max Lam, Gabriela Sánchez-Andrade, Tarjinder Singh +76 more

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.009

N/A

0.617DataRank · unranked

60 citations

Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen‐Chen Anne Feng +95 more

Omics Approaches to Investigate the Pathogenesis of Suicide

Biological Psychiatry(2024)10.1016/j.biopsych.2024.05.017

N/A

0.473DataRank · unranked

10 citations

Yang Xiao, Tarjinder Singh, Chenxu Zhu, Mbemba Jabbi, Harry Pantazopoulos +16 more

ASD and ADHD have a similar burden of rare protein-truncating variants

bioRxiv (Cold Spring Harbor Laboratory)(2018)10.1101/277707

N/A

0.434DataRank · unranked

17 citations

Tarjinder Singh, Emilie M. Wigdor, Jurgen Del‐Favero, Ditte Demontis, Christine Stevens +18 more

Exome sequencing in bipolar disorder reveals shared risk gene AKAP11 with schizophrenia

medRxiv(2021)10.1101/2021.03.09.21252930

N/A

0.366DataRank · unranked

7 citations

Daniel P. Howrigan, Sinéad B. Chapman, Rolf Adolfsson, Nick Bass, Douglas Blackwood +41 more

Genetic contribution to disease-course severity and progression in the SUPER-Finland study, a cohort of 10,403 individuals with psychotic disorders

Molecular Psychiatry(2024)10.1038/s41380-024-02516-6

N/A

0.360DataRank · unranked

10 citations

Jaana Suvisaari, Markku Lähteenvuo, Tarjinder Singh, Ari Ahola‐Olli, Lea Urpa +33 more

The genetic architecture of the human skeletal form

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.01.03.521284

N/A

0DataRank · unranked

2 citations

Emily Javan, Olivia S. Smith, Faris F. Gulamali, Javier de la Fuente, Brianna I. Flynn +8 more

Deep learning based phenotyping of medical images improves power for gene discovery of complex disease

medRxiv(2023)10.1101/2023.03.07.23286909

N/A

0DataRank · unranked

1 citations

Emily Javan, Eugenia Lin, Zoe Trutner, Karl Koenig, Kenoma O. Anighoro +6 more

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

UNC Libraries(2024)10.17615/4nb8-at41

N/A

0DataRank · unranked

0 citations

David Curtis, Jennifer Sambrook, Robin Murray, David St Clair, Trevor Cole +54 more

Characterization of six CaMKIIα variants found in patients with schizophrenia

iScience(2021)10.1016/j.isci.2021.103184

N/A

0DataRank · unranked

19 citations

Sarah G. Cook, Hillary F. Allen, Kevin C. Crosby, Tarjinder Singh, Steven J. Coultrap +2 more

Deep learning based phenotyping of medical images improves power for gene discovery of complex disease

npj Digital Medicine(2023)10.1038/s41746-023-00903-x

N/A

0DataRank · unranked

14 citations

Emily Javan, Eugenia Lin, Zoe Trutner, Karl Koenig, Kenoma O. Anighoro +6 more