Nancy B. Spinner

MedicineBiochemistry, 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

1in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 1 indexed paper attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

Papers

Driven by 15 papers. Top paper: “Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia”.

Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

Science(2008)10.1126/science.1155174

N/A

1.1DataRank · unranked

1822 citations

Anjene M Addington, Wellcome Trust Case Control Consortium, Anjené M. Addington, Sarah B. Pierce, Alex S. Nord +39 more

Microduplications of 16p11.2 are associated with schizophrenia

Nature Genetics(2009)10.1038/ng.474

N/A

0.990DataRank · unranked

733 citations

Kenneth S. Kendler, Manfred Kayser, Anjene M Addington, Jon McClellan, Milica Pejović-Milovančević +66 more

A six-attribute classification of geneticmosaicism

Genetics in Medicine(2020)10.1038/s41436-020-0877-3

N/A

0.668DataRank · unranked

85 citations

Jair Tenorio, Julián Nevado, Gema Gordo, Lara Rodríguez‐Laguna, Marta Feito +9 more

Impaired Redox and Protein Homeostasis as Risk Factors and Therapeutic Targets in Toxin-Induced Biliary Atresia

Gastroenterology(2020)10.1053/j.gastro.2020.05.080

N/A

0.489DataRank · unranked

25 citations

Kristin Lorent, Diana Escobar-Zarate, Ramakrishnan Rajagopalan, Kathleen M. Loomes, Kevin P. Gillespie +8 more

Exome Sequencing in Individuals with Isolated Biliary Atresia

Scientific Reports(2020)10.1038/s41598-020-59379-4

N/A

0.457DataRank · unranked

20 citations

Ellen Tsai, Christopher M. Grochowski, Susan M. Kelly, Kathleen M. Loomes, Nancy B. Spinner +2 more

Functional characterization of 2,832 JAG1 variants supports reclassification for Alagille syndrome and improves guidance for clinical variant interpretation

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.06.011

N/A

0.416DataRank · unranked

15 citations

Ernest Keefer-Jacques, Tanaya Jadhav, Daniel Antfolk, Qianqian Ming, Nicolette Valente +9 more

Phenotypic Divergence of JAG1 ‐ and NOTCH2 ‐Associated Alagille Syndrome & Disease‐Specific NOTCH2 Variant Classification Guidelines

Liver International(2025)10.1111/liv.70251

N/A

0.241DataRank · unranked

4 citations

Liting Li, Huiyu She, Jian‐She Wang, Kathleen M. Loomes, David A. Piccoli +87 more

Microduplications of 16p11.2 are associated with schizophrenia

UNC Libraries(2020)10.17615/zwts-m549

N/A

0DataRank · unranked

0 citations

Jaya Ganesh, Detelina Grozeva, Vladimir Makarov, Abhishek Bhandari, Ravinesh A. Kumar +27 more

Processes and preliminary outputs for identification of actionable genes as incidental findings in genomic sequence data in the Clinical Sequencing Exploratory Research Consortium

UNC Libraries(2020)10.17615/x7nz-xc34

N/A

0DataRank · unranked

0 citations

Levi A. Garraway, Elizabeth T. DeChene, Heidi L. Rehm, Matthew C. Dulik, James P. Evans +12 more

Advanced approach for comprehensive mtDNA genome testing in mitochondrial disease

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.12.006

N/A

0DataRank · unranked

29 citations

Jorune Balciuniene, Maria Alejandra Diaz‐Miranda, Elizabeth M. McCormick, Erfan Aref-Eshghi, Alison M. Muir +14 more

Generation of an Alagille syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi032-A) carrying a heterozygous mutation (p.Cys682Leufs*7) in the JAG1 gene

Stem Cell Research(2023)10.1016/j.scr.2023.103231

N/A

0DataRank · unranked

4 citations

Ivan Pavlinov, Miao Xu, Kaari L. Linask, Jeanette Beers, Chengyu Liu +7 more

Generation of an Alagille Syndrome (ALGS) patient-derived induced pluripotent stem cell line (TRNDi036-A) carrying a heterozygous mutation (p.Cys693*) in the JAG1 gene

Stem Cell Research(2024)10.1016/j.scr.2024.103429

N/A

0DataRank · unranked

2 citations

Miao Xu, Ivan Pavlinov, Kaari L. Linask, Jeanette Beers, Jizhong Zou +8 more

Generation of induced pluripotent stem cell lines TRNDi037-A and TRNDi038-A from two patients with Alagille syndrome carrying heterozygous JAG1 mutations

Stem Cell Research(2024)10.1016/j.scr.2024.103634

N/A

0DataRank · unranked

0 citations

Guibin Chen, Ivan Pavlinov, Xiuli Huang, Kaari L. Linask, Chengyu Liu +9 more

Alagille syndrome and risk for hepatocellular carcinoma: Need for increased surveillance in adults with mild liver phenotypes

American Journal of Medical Genetics Part A(2020)10.1002/ajmg.a.62028

N/A

0DataRank · unranked

28 citations

Melissa A. Gilbert, David A. Piccoli, Nancy B. Spinner, Ian D. Krantz, Kathleen M. Loomes +1 more

Outcomes of Childhood Cholestasis in Alagille Syndrome: Results of a Multicenter Observational Study

Hepatology Communications(2020)10.1002/hep4.1468

N/A

0DataRank · unranked

81 citations

Wen Ye, Nathan P. Goodrich, Kathleen M. Loomes, René Romero, James E. Heubi +17 more