Aaron Black

3.5k total citations
10 papers, 264 citations indexed

About

Aaron Black is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Aaron Black has authored 10 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Aaron Black's work include Genomics and Rare Diseases (4 papers), Retinal Development and Disorders (3 papers) and RNA modifications and cancer (2 papers). Aaron Black is often cited by papers focused on Genomics and Rare Diseases (4 papers), Retinal Development and Disorders (3 papers) and RNA modifications and cancer (2 papers). Aaron Black collaborates with scholars based in United States, Netherlands and Australia. Aaron Black's co-authors include Jean Bennett, Anneke I. den Hollander, Frans P.M. Cremers, A. O. B. Redmond, Gareth Roberts, Vidyullatha Vasireddy, Albert M. Maguire, Miguel C. Seabra, Daniel C. Chung and Thierry Vilboux and has published in prestigious journals such as Journal of Clinical Investigation, PEDIATRICS and Trends in Molecular Medicine.

In The Last Decade

Aaron Black

10 papers receiving 257 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Aaron Black United States 5 209 107 83 37 32 10 264
Lucas Fares‐Taie France 8 177 0.8× 32 0.3× 86 1.0× 18 0.5× 16 0.5× 15 238
Firoz Kabir United States 11 193 0.9× 98 0.9× 57 0.7× 49 1.3× 11 0.3× 23 258
Saoud Tahsin Swafiri Spain 11 175 0.8× 61 0.6× 98 1.2× 15 0.4× 7 0.2× 15 252
Zachry T. Soens United States 9 249 1.2× 111 1.0× 161 1.9× 21 0.6× 26 0.8× 12 325
Inmaculada Martín-Mérida Spain 10 225 1.1× 95 0.9× 77 0.9× 22 0.6× 14 0.4× 15 251
A. S. Jun United States 6 290 1.4× 63 0.6× 38 0.5× 122 3.3× 43 1.3× 8 416
Galuh Astuti Netherlands 12 340 1.6× 142 1.3× 106 1.3× 42 1.1× 56 1.8× 23 423
Wouter Beumer Netherlands 8 195 0.9× 32 0.3× 41 0.5× 12 0.3× 35 1.1× 11 252
Ingrid Bader Germany 7 186 0.9× 61 0.6× 69 0.8× 13 0.4× 18 0.6× 12 206
Sara D. Ragi United States 8 173 0.8× 72 0.7× 39 0.5× 27 0.7× 55 1.7× 33 246

Countries citing papers authored by Aaron Black

Since Specialization
Citations

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

Fields of papers citing papers by Aaron Black

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aaron Black

This figure shows the co-authorship network connecting the top 25 collaborators of Aaron Black. A scholar is included among the top collaborators of Aaron Black 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 Aaron Black. Aaron Black 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
1.
Durham, Emily L., et al.. (2023). TBCK syndrome: a rare multi-organ neurodegenerative disease. Trends in Molecular Medicine. 29(10). 783–785. 4 indexed citations
2.
Nair, Divya, Aaron Black, Rajesh Angireddy, et al.. (2023). Heterozygous variants in TBCK cause a mild neurologic syndrome in humans and mice. American Journal of Medical Genetics Part A. 191(10). 2508–2517. 2 indexed citations
4.
Bodian, Dale L., Thierry Vilboux, Alina Khromykh, et al.. (2017). Utilization of genomic sequencing for population screening of immunodeficiencies in the newborn. Genetics in Medicine. 19(12). 1367–1375. 22 indexed citations
5.
Solomon, Benjamin D., Dale L. Bodian, Alina Khromykh, et al.. (2016). Utility of Whole Genome Sequencing for Detection of Newborn Screening Disorders in a Population Cohort of ∼1700 Neonates. PEDIATRICS. 137(Supplement 3). 492A–492A. 1 indexed citations
6.
Cherukuri, Praveen F., Thierry Vilboux, Prachi Kothiyal, et al.. (2016). P-B23 Prevalence of Ebola viral entry resistance in a diverse population. JAIDS Journal of Acquired Immune Deficiency Syndromes. 71(Supplement 1). 83–83. 1 indexed citations
7.
Black, Aaron, Vidyullatha Vasireddy, Daniel C. Chung, et al.. (2014). Adeno‐associated virus 8‐mediated gene therapy for choroideremia: preclinical studies in in vitro and in vivo models. The Journal of Gene Medicine. 16(5-6). 122–130. 30 indexed citations
8.
Hollander, Anneke I. den, Aaron Black, Jean Bennett, & Frans P.M. Cremers. (2010). Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies. Journal of Clinical Investigation. 120(9). 3042–3053. 166 indexed citations
9.
Hollander, Anneke I. den, Aaron Black, Jean Bennett, & Frans P.M. Cremers. (2010). Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies. Journal of Clinical Investigation. 121(1). 456–456. 9 indexed citations
10.
Roberts, Gareth, et al.. (1988). Screening for cystic fibrosis: a four year regional experience.. Archives of Disease in Childhood. 63(12). 1438–1443. 28 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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