T. Blaine Crowley

2.2k total citations
52 papers, 558 citations indexed

About

T. Blaine Crowley is a scholar working on Molecular Biology, Epidemiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, T. Blaine Crowley has authored 52 papers receiving a total of 558 indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Molecular Biology, 35 papers in Epidemiology and 28 papers in Pulmonary and Respiratory Medicine. Recurrent topics in T. Blaine Crowley's work include Congenital heart defects research (46 papers), Congenital Heart Disease Studies (35 papers) and Coronary Artery Anomalies (18 papers). T. Blaine Crowley is often cited by papers focused on Congenital heart defects research (46 papers), Congenital Heart Disease Studies (35 papers) and Coronary Artery Anomalies (18 papers). T. Blaine Crowley collaborates with scholars based in United States, Italy and Canada. T. Blaine Crowley's co-authors include Donna M. McDonald‐McGinn, Elaine H. Zackai, Beverly S. Emanuel, Daniel E. McGinn, Kathleen E. Sullivan, Raquel E. Gur, Jennifer Heimall, Cynthia Solot, Marta Unolt and Kathleen Valverde and has published in prestigious journals such as SHILAP Revista de lepidopterología, Gastroenterology and Scientific Reports.

In The Last Decade

T. Blaine Crowley

49 papers receiving 557 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
T. Blaine Crowley United States 15 424 267 190 165 99 52 558
Moira Blyth United Kingdom 12 139 0.3× 68 0.3× 75 0.4× 162 1.0× 57 0.6× 22 379
Friederike Körber Germany 11 116 0.3× 60 0.2× 56 0.3× 137 0.8× 63 0.6× 32 424
Christopher Troedson Australia 13 147 0.3× 125 0.5× 33 0.2× 83 0.5× 31 0.3× 29 524
Eugene J. Sidoti United States 6 396 0.9× 165 0.6× 217 1.1× 396 2.4× 107 1.1× 8 647
Agata Polizzi Italy 15 183 0.4× 87 0.3× 14 0.1× 190 1.2× 117 1.2× 36 590
Julie M. Joyce Canada 10 176 0.4× 88 0.3× 20 0.1× 174 1.1× 18 0.2× 26 470
M. Hariri United Kingdom 7 60 0.1× 64 0.2× 497 2.6× 160 1.0× 60 0.6× 8 725
Kwang-Jen Hsiao Taiwan 14 279 0.7× 33 0.1× 44 0.2× 87 0.5× 136 1.4× 37 667
Jane C. Edmond United States 14 122 0.3× 94 0.4× 28 0.1× 170 1.0× 85 0.9× 37 498
Frédérique Toulgoat France 14 53 0.1× 106 0.4× 59 0.3× 40 0.2× 104 1.1× 24 703

Countries citing papers authored by T. Blaine Crowley

Since Specialization
Citations

This map shows the geographic impact of T. Blaine Crowley'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 T. Blaine Crowley with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites T. Blaine Crowley more than expected).

Fields of papers citing papers by T. Blaine Crowley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by T. Blaine Crowley. 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 T. Blaine Crowley. The network helps show where T. Blaine Crowley may publish in the future.

Co-authorship network of co-authors of T. Blaine Crowley

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

All Works

20 of 20 papers shown
1.
White, Lauren K., T. Blaine Crowley, Brenda Finucane, et al.. (2023). Gathering the Stakeholder’s Perspective: Experiences and Opportunities in Rare Genetic Disease Research. Genes. 14(1). 169–169. 2 indexed citations
2.
Gur, Raquel E., Raquel E. Gur, Donna M. McDonald‐McGinn, et al.. (2023). Psychosis spectrum features, neurocognition and functioning in a longitudinal study of youth with 22q11.2 deletion syndrome. Psychological Medicine. 53(14). 6763–6772. 6 indexed citations
3.
Blagowidow, Natalie, Beata Nowakowska, Erica Schindewolf, et al.. (2023). Prenatal Screening and Diagnostic Considerations for 22q11.2 Microdeletions. Genes. 14(1). 160–160. 15 indexed citations
4.
Surrey, Lea F., Abhay Srinivasan, Dong Li, et al.. (2023). Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CA. American Journal of Medical Genetics Part A. 194(1). 64–69. 1 indexed citations
5.
Solot, Cynthia, T. Blaine Crowley, Jeroen Breckpot, et al.. (2023). Language Profiles of School-Aged Children with 22q11.2 Copy Number Variants. Genes. 14(3). 679–679. 6 indexed citations
6.
McGinn, Daniel E., T. Blaine Crowley, Tracy Heung, et al.. (2022). Influence of Parent-of-Origin on Intellectual Outcomes in the Chromosome 22q11.2 Deletion Syndrome. Genes. 13(10). 1800–1800. 2 indexed citations
7.
Campbell, Ian M., T. Blaine Crowley, Chintan Jobaliya, et al.. (2022). Platelet findings in 22q11.2 deletion syndrome correlate with disease manifestations but do not correlate with GPIb surface expression. Clinical Genetics. 103(1). 109–113. 4 indexed citations
8.
Crowley, T. Blaine, Yichuan Liu, Marta Unolt, et al.. (2022). Improved Outcomes in Patients with 22q11.2 Deletion Syndrome and Diagnosis of Interrupted Aortic Arch Prior to Birth Hospital Discharge, a Retrospective Study. Genes. 14(1). 62–62. 7 indexed citations
9.
Crowley, T. Blaine, et al.. (2022). Surgical insights and management in patients with the 22q11.2 deletion syndrome. Pediatric Surgery International. 38(6). 899–905. 2 indexed citations
10.
Homans, Jelle F., Tom P. C. Schlösser, Michiel L. Houben, et al.. (2021). 22q11.2 Deletion Syndrome as a Human Model for Idiopathic Scoliosis. Journal of Clinical Medicine. 10(21). 4823–4823. 5 indexed citations
11.
Schmitt, J. Eric, David R. Roalf, Kosha Ruparel, et al.. (2021). A Comprehensive Analysis of Cerebellar Volumes in the 22q11.2 Deletion Syndrome. Biological Psychiatry Cognitive Neuroscience and Neuroimaging. 8(1). 79–90. 7 indexed citations
12.
Zhang, Zhe, Lihua Shi, Li Song, et al.. (2021). Chromatin Modifications in 22q11.2 Deletion Syndrome. Journal of Clinical Immunology. 41(8). 1853–1864. 12 indexed citations
13.
Solot, Cynthia, Tyler M. Moore, T. Blaine Crowley, et al.. (2020). Early language measures associated with later psychosis features in 22q11.2 deletion syndrome. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 183(6). 392–400. 12 indexed citations
14.
Unolt, Marta, Molka Kammoun, Beata Nowakowska, et al.. (2019). Pathogenic variants in CDC45 on the remaining allele in patients with a chromosome 22q11.2 deletion result in a novel autosomal recessive condition. Genetics in Medicine. 22(2). 326–335. 7 indexed citations
15.
Elden, Lisa M., T. Blaine Crowley, Frank A. Pameijer, et al.. (2018). Anatomic Malformations of the Middle and Inner Ear in 22q11.2 Deletion Syndrome: Case Series and Literature Review. American Journal of Neuroradiology. 39(5). 928–934. 14 indexed citations
16.
Cohen, Jennifer L., T. Blaine Crowley, Daniel E. McGinn, et al.. (2018). 22q and two: 22q11.2 deletion syndrome and coexisting conditions. American Journal of Medical Genetics Part A. 176(10). 2203–2214. 21 indexed citations
17.
Schindewolf, Erica, Nahla Khalek, Mark P. Johnson, et al.. (2018). Expanding the fetal phenotype: Prenatal sonographic findings and perinatal outcomes in a cohort of patients with a confirmed 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 176(8). 1735–1741. 30 indexed citations
18.
Unolt, Marta, Paolo Versacci, Silvia Anaclerio, et al.. (2018). Congenital heart diseases and cardiovascular abnormalities in 22q11.2 deletion syndrome: From well‐established knowledge to new frontiers. American Journal of Medical Genetics Part A. 176(10). 2087–2098. 43 indexed citations
19.
Sacca, Rosalba, Karen B. Zur, T. Blaine Crowley, et al.. (2017). Association of airway abnormalities with 22q11.2 deletion syndrome. International Journal of Pediatric Otorhinolaryngology. 96. 11–14. 32 indexed citations
20.
Crowley, T. Blaine, Soma Jyonouchi, Jennifer Heimall, et al.. (2017). Identification of 22q11.2 Deletion Syndrome via Newborn Screening for Severe Combined Immunodeficiency. Journal of Clinical Immunology. 37(5). 476–485. 34 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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