Marcia Blair

2.4k total citations
34 papers, 969 citations indexed

About

Marcia Blair is a scholar working on Cardiology and Cardiovascular Medicine, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Marcia Blair has authored 34 papers receiving a total of 969 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Cardiology and Cardiovascular Medicine, 7 papers in Cellular and Molecular Neuroscience and 6 papers in Molecular Biology. Recurrent topics in Marcia Blair's work include Cardiac electrophysiology and arrhythmias (13 papers), Atrial Fibrillation Management and Outcomes (12 papers) and Cardiac Arrhythmias and Treatments (8 papers). Marcia Blair is often cited by papers focused on Cardiac electrophysiology and arrhythmias (13 papers), Atrial Fibrillation Management and Outcomes (12 papers) and Cardiac Arrhythmias and Treatments (8 papers). Marcia Blair collaborates with scholars based in United States, Denmark and Australia. Marcia Blair's co-authors include Dan M. Roden, Dawood Darbar, Peter Hedera, Shaochun Ma, Raafia Muhammad, Tanya Stubblefield, Jonathan L. Haines, Jessica Delaney, Tao Yang and M. Benjamin Shoemaker and has published in prestigious journals such as Circulation, Journal of the American College of Cardiology and Neurology.

In The Last Decade

Marcia Blair

34 papers receiving 946 citations

Peers

Countries citing papers authored by Marcia Blair

Since Specialization

Citations

This map shows the geographic impact of Marcia Blair'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 Marcia Blair with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marcia Blair more than expected).

Fields of papers citing papers by Marcia Blair

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marcia Blair. 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 Marcia Blair. The network helps show where Marcia Blair may publish in the future.

Co-authorship network of co-authors of Marcia Blair

This figure shows the co-authorship network connecting the top 25 collaborators of Marcia Blair. A scholar is included among the top collaborators of Marcia Blair 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 Marcia Blair. Marcia Blair is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	High-throughput discovery of trafficking-deficient variants in the cardiac potassium channel KV11.1 2020 ·Heart Rhythm ·Krystian A. Kozek, Andrew M. Glazer, Chai‐Ann Ng, Daniel J. Blackwell, (unknown), (unknown), Marcia Blair, (unknown), Kenneth A. Matreyek, Douglas M. Fowler, Björn C. Knollmann, Jamie I. Vandenberg, Dan M. Roden, Brett M. Kroncke	32
2	High-Throughput Reclassification of SCN5A Variants 2020 ·The American Journal of Human Genetics ·Andrew M. Glazer, Yuko Wada, Bian Li, (unknown), (unknown), Matthew J. O’Neill, Tiffany Shields, Lynn Hall, Laura Short, Marcia Blair, Brett M. Kroncke, John A. Capra, Dan M. Roden	83
3	Electrophysiologic and molecular mechanisms of a frameshift NPPA mutation linked with familial atrial fibrillation 2019 ·Journal of Molecular and Cellular Cardiology ·(unknown), Liang Hong, Eleonora Savio‐Galimberti, Arvind Sridhar, Seock‐Won Youn, Meihong Zhang, (unknown), Marcia Blair, Sabina Kupershmidt, Dawood Darbar	22
4	INITIAL CHANGES IN PEAK AORTIC JET VELOCITY AND MEAN GRADIENT PREDICT PROGRESSION TO SEVERE AORTIC STENOSIS 2019 ·Journal of the American College of Cardiology ·(unknown), (unknown), Xu Meng, Eric Farber‐Eger, Marcia Blair, (unknown), Gregg C. Fonarow, (unknown), John McPherson, Quinn S. Wells	3
5	SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation 2014 ·Cardiovascular Research ·Eleonora Savio‐Galimberti, Peter Weeke, Raafia Muhammad, Marcia Blair, (unknown), Laura Short, Thomas C. Atack, (unknown), Carlos G. Vanoye, Morten S. Olesen, (unknown), Tao Yang, Alfred L. George, Dan M. Roden, Dawood Darbar	52
6	Whole-exome sequencing in familial atrial fibrillation 2014 ·European Heart Journal ·Peter Weeke, Raafia Muhammad, Jessica Delaney, Christian M. Shaffer, Jonathan D. Mosley, Marcia Blair, Laura Short, Tanya Stubblefield, Dan M. Roden, Dawood Darbar	31
7	A Genome-Wide Association Study to Identify Genomic Modulators of Rate Control Therapy in Patients With Atrial Fibrillation 2014 ·The American Journal of Cardiology ·Matthew J. Kolek, Todd L. Edwards, Raafia Muhammad, (unknown), M. Benjamin Shoemaker, Marcia Blair, (unknown), Atsushi Takahashi, Michiaki Kubo, Dan M. Roden, Toshihiro Tanaka, Dawood Darbar	9
8	Common genetic polymorphism at 4q25 locus predicts atrial fibrillation recurrence after successful cardioversion 2013 ·Heart Rhythm ·Babar Parvez, M. Benjamin Shoemaker, Raafia Muhammad, (unknown), Lan Jiang, Marcia Blair, Dan M. Roden, Dawood Darbar	61
9	Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation 2013 ·Heart Rhythm ·Peter Weeke, Babar Parvez, Marcia Blair, Laura Short, (unknown), Gayle Kucera, Tanya Stubblefield, Dan M. Roden, Dawood Darbar	12
10	A Common Variant on Chromosome 4q25 is Associated With Prolonged PR Interval in Subjects With and Without Atrial Fibrillation 2013 ·The American Journal of Cardiology ·Matthew J. Kolek, Babar Parvez, Raafia Muhammad, M. Benjamin Shoemaker, Marcia Blair, Tanya Stubblefield, Gayle Kucera, Joshua C. Denny, Dan M. Roden, Dawood Darbar	15
11	Abstract 19074: NPPA Overexpression in Mice Increases Susceptibility to Atrial Fibrillation 2012 ·Circulation ·Eleonora Savio‐Galimberti, Prince J. Kannankeril, (unknown), Raafia Muhammad, Marcia Blair, Dawood Darbar	1
12	Chromosome 4q25 Variants Are Genetic Modifiers of Rare Ion Channel Mutations Associated With Familial Atrial Fibrillation 2012 ·Journal of the American College of Cardiology ·Marylyn D. Ritchie, Shane Rowan, Gayle Kucera, Tanya Stubblefield, Marcia Blair, Shannon Carter, Dan M. Roden, Dawood Darbar	60
13	A KCNJ8 mutation associated with early repolarization and atrial fibrillation 2012 ·EP Europace ·Jessica Delaney, (unknown), Marcia Blair, (unknown), Frank A. Fish, Dan M. Roden, Dawood Darbar	90
14	Reappraisal of the role of the DRD3 gene in essential tremor 2008 ·Parkinsonism & Related Disorders ·Marcia Blair, Shaochun Ma, Fenna T. Phibbs, John Y. Fang, Michael K. Cooper, Thomas L. Davis, Peter Hedera	25
15	Infantile Onset of Hereditary Spastic Paraplegia Poorly Predicts the Genotype 2007 ·Pediatric Neurology ·Marcia Blair, (unknown), (unknown), (unknown), Peter Hedera	17
16	Identification of a Novel Locus for Febrile Seizures and Epilepsy on Chromosome 21q22 2006 ·Epilepsia ·Peter Hedera, Shaochun Ma, Marcia Blair, (unknown), (unknown), Yuki Bradford, Bassel Abou‐Khalil, Jonathan L. Haines	34
17	Familial essential tremor with apparent autosomal dominant inheritance: Should we also consider other inheritance modes? 2006 ·Movement Disorders ·Shaochun Ma, Thomas L. Davis, Marcia Blair, John Y. Fang, Yuki Bradford, Jonathan L. Haines, Peter Hedera	35
18	Mutation in KIF5A can also cause adult-onset hereditary spastic paraplegia 2006 ·Neurogenetics ·Marcia Blair, Shaochun Ma, Peter Hedera	42
19	Mutations in GABRA1, GABRA5, GABRG2 and GABRD receptor genes are not a major factor in the pathogenesis of familial focal epilepsy preceded by febrile seizures 2005 ·Neuroscience Letters ·Shaochun Ma, Bassel Abou‐Khalil, Marcia Blair, James S. Sutcliffe, Jonathan L. Haines, Peter Hedera	14
20	Novel Mutation in the SPG3A Gene in an African American Family With an Early Onset of Hereditary Spastic Paraplegia 2004 ·Archives of Neurology ·Peter Hedera, Gerald M. Fenichel, Marcia Blair, Jonathan L. Haines	22

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.

Explore authors with similar magnitude of impact