Debbie A. Nickerson

2.9k total citations
10 papers, 371 citations indexed

About

Debbie A. Nickerson is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Rheumatology. According to data from OpenAlex, Debbie A. Nickerson has authored 10 papers receiving a total of 371 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Pulmonary and Respiratory Medicine and 2 papers in Rheumatology. Recurrent topics in Debbie A. Nickerson's work include Chromosomal and Genetic Variations (2 papers), Cancer Genomics and Diagnostics (2 papers) and Iron Metabolism and Disorders (2 papers). Debbie A. Nickerson is often cited by papers focused on Chromosomal and Genetic Variations (2 papers), Cancer Genomics and Diagnostics (2 papers) and Iron Metabolism and Disorders (2 papers). Debbie A. Nickerson collaborates with scholars based in United States, Canada and Australia. Debbie A. Nickerson's co-authors include Mark J. Rieder, Brian J. O’Roak, Emre Karakoç, Kenneth M. K. Mark, Laura Vives, Can Alkan, Evan E. Eichler, Megan Y. Dennis, J. G. Smith and Habil Zare and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Nature Methods.

In The Last Decade

Debbie A. Nickerson

10 papers receiving 366 citations

Peers

Debbie A. Nickerson
Hilmi Tozkır Türkiye
Stacy Roberts United States
Eddy N. de Boer Netherlands
Nan Leng China
Esther Vamos Belgium
Fang Xu China
Debbie A. Nickerson
Citations per year, relative to Debbie A. Nickerson Debbie A. Nickerson (= 1×) peers Emmanouil Kanavakis

Countries citing papers authored by Debbie A. Nickerson

Since Specialization
Citations

This map shows the geographic impact of Debbie A. Nickerson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Debbie A. Nickerson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Debbie A. Nickerson more than expected).

Fields of papers citing papers by Debbie A. Nickerson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Debbie A. Nickerson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Debbie A. Nickerson. The network helps show where Debbie A. Nickerson may publish in the future.

Co-authorship network of co-authors of Debbie A. Nickerson

This figure shows the co-authorship network connecting the top 25 collaborators of Debbie A. Nickerson. A scholar is included among the top collaborators of Debbie A. Nickerson based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Debbie A. Nickerson. Debbie A. Nickerson is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

10 of 10 papers shown
2.
Patowary, Ashok, Ryan Nesbitt, Debbie A. Nickerson, et al.. (2019). Family-based exome sequencing and case-control analysis implicate CEP41 as an ASD gene. Translational Psychiatry. 9(1). 4–4. 11 indexed citations
3.
Wallace, Stephanie E, Dong Guo, Ellen S. Regalado, et al.. (2016). Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension. Clinical Genetics. 90(4). 351–360. 53 indexed citations
4.
Emond, Mary J., Tin Louie, Julia Emerson, et al.. (2015). Exome Sequencing of Phenotypic Extremes Identifies CAV2 and TMC6 as Interacting Modifiers of Chronic Pseudomonas aeruginosa Infection in Cystic Fibrosis. PLoS Genetics. 11(6). e1005273–e1005273. 33 indexed citations
5.
Blau, C. Anthony, Habil Zare, Junfeng Wang, et al.. (2014). Inferring clonal composition from multiple sections of a breast cancer.. Journal of Clinical Oncology. 32(15_suppl). 11077–11077. 4 indexed citations
6.
Zare, Habil, Junfeng Wang, Alex Hu, et al.. (2014). Inferring Clonal Composition from Multiple Sections of a Breast Cancer. PLoS Computational Biology. 10(7). e1003703–e1003703. 75 indexed citations
7.
Murray, Joseph A., Stela McLachlan, Paul C. Adams, et al.. (2013). Association Between Celiac Disease and Iron Deficiency in Caucasians, but Not Non-Caucasians. Clinical Gastroenterology and Hepatology. 11(7). 808–814. 27 indexed citations
8.
Karakoç, Emre, Can Alkan, Brian J. O’Roak, et al.. (2011). Detection of structural variants and indels within exome data. Nature Methods. 9(2). 176–178. 82 indexed citations
9.
McLaren, Christine E., Chad Garner, Clare C. Constantine, et al.. (2011). Genome-Wide Association Study Identifies Genetic Loci Associated with Iron Deficiency. PLoS ONE. 6(3). e17390–e17390. 53 indexed citations
10.
Cushman, Mary, Leslie A. Lange, Lucia A. Hindorff, et al.. (2008). Associations between common fibrinogen gene polymorphisms and cardiovascular disease in older adults. Thrombosis and Haemostasis. 99(2). 388–395. 32 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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