Brad Angle

2.6k total citations
33 papers, 1000 citations indexed

About

Brad Angle is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Brad Angle has authored 33 papers receiving a total of 1000 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 16 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Brad Angle's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (7 papers) and RNA modifications and cancer (4 papers). Brad Angle is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (7 papers) and RNA modifications and cancer (4 papers). Brad Angle collaborates with scholars based in United States, Germany and Poland. Brad Angle's co-authors include Barbara K. Burton, Zsolt Urbán, Vishwanathan Hucthagowder, Katherine H. Kim, Lihua Y. Marmorstein, Nina Sausgruber, Laurence I. Burd, Joseph H. Hersh, Katherine Christensen and Joel Charrow and has published in prestigious journals such as PEDIATRICS, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Brad Angle

32 papers receiving 975 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Brad Angle United States 18 527 444 191 117 107 33 1000
Louise C. Wilson United Kingdom 20 638 1.2× 629 1.4× 178 0.9× 104 0.9× 88 0.8× 46 1.2k
B. Le Marec France 19 474 0.9× 506 1.1× 115 0.6× 150 1.3× 88 0.8× 67 1.0k
Gary A. Bellus United States 19 1.3k 2.5× 1.3k 3.0× 215 1.1× 130 1.1× 139 1.3× 30 2.0k
Irfan Saadi United States 18 347 0.7× 623 1.4× 57 0.3× 75 0.6× 94 0.9× 36 1.1k
Maria Iascone Italy 20 320 0.6× 608 1.4× 265 1.4× 57 0.5× 105 1.0× 115 1.5k
Marco Ritelli Italy 25 1.1k 2.0× 474 1.1× 245 1.3× 61 0.5× 221 2.1× 79 1.6k
Boris G. Kousseff United States 25 785 1.5× 603 1.4× 307 1.6× 276 2.4× 96 0.9× 83 1.6k
C Camacho-Hübner United Kingdom 12 181 0.3× 409 0.9× 113 0.6× 73 0.6× 44 0.4× 16 1.0k
Nicola Chiarelli Italy 22 724 1.4× 340 0.8× 158 0.8× 25 0.2× 96 0.9× 40 1.0k
Kouji Narahara Japan 18 500 0.9× 509 1.1× 50 0.3× 212 1.8× 54 0.5× 52 877

Countries citing papers authored by Brad Angle

Since Specialization
Citations

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

Fields of papers citing papers by Brad Angle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Brad Angle

This figure shows the co-authorship network connecting the top 25 collaborators of Brad Angle. A scholar is included among the top collaborators of Brad Angle 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 Brad Angle. Brad Angle 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.
Torres, Raúl, Rotem Ben‐Shachar, Jodi D. Hoffman, et al.. (2020). Evaluation and classification of severity for 176 genes on an expanded carrier screening panel. Prenatal Diagnosis. 40(10). 1246–1257. 28 indexed citations
2.
Beck, David B., Megan T. Cho, Francisca Millan, et al.. (2016). A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects. Neurogenetics. 17(3). 173–178. 25 indexed citations
3.
Millan, Francisca, Megan T. Cho, Kyle Retterer, et al.. (2016). Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder. American Journal of Medical Genetics Part A. 170(7). 1791–1798. 42 indexed citations
4.
Weh, Eric, Linda M. Reis, Hannah C. Happ, et al.. (2014). Whole exome sequence analysis of Peters anomaly. Human Genetics. 133(12). 1497–1511. 53 indexed citations
5.
Peña, Loren, Brad Angle, Barbara K. Burton, & Joel Charrow. (2012). Follow-up of patients with short-chain acyl-CoA dehydrogenase and isobutyryl-CoA dehydrogenase deficiencies identified through newborn screening: one center’s experience. Genetics in Medicine. 14(3). 342–347. 22 indexed citations
6.
Burton, Barbara K., et al.. (2012). A Pilot Newborn Screening Program for Lysosomal Storage Disorders (LSD) in Illinois. Molecular Genetics and Metabolism. 105(2). S23–S24. 16 indexed citations
7.
Rosenfeld, Jill A., Kyae Hyung Kim, Brad Angle, et al.. (2012). Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly. Molecular Syndromology. 3(6). 247–254. 37 indexed citations
8.
Rosenfeld, Jill A., Brad Angle, Valerie Banks, et al.. (2011). Distinctive phenotype in 9 patients with deletion of chromosome 1q24‐q25. American Journal of Medical Genetics Part A. 155(6). 1336–1351. 29 indexed citations
9.
Epstein, Leon G., Ali Jalali, Joshua V. Ross, et al.. (2008). Neuroimaging findings in children with rare or novel de novo chromosomal anomalies. Birth Defects Research Part A Clinical and Molecular Teratology. 82(4). 200–210. 1 indexed citations
10.
Angle, Brad & Barbara K. Burton. (2007). Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II. Molecular Genetics and Metabolism. 93(1). 36–39. 46 indexed citations
11.
Oglesbee, Devin, Miao He, Jerry Vockley, et al.. (2007). Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiency. Genetics in Medicine. 9(2). 108–116. 33 indexed citations
12.
Angle, Brad. (2007). A 4-month-old Girl With an Enlarged Tongue and Limb Asymmetry. Pediatric Annals. 36(5). 261–262. 2 indexed citations
13.
Hucthagowder, Vishwanathan, Nina Sausgruber, Katherine H. Kim, et al.. (2006). Fibulin-4: A Novel Gene for an Autosomal Recessive Cutis Laxa Syndrome. The American Journal of Human Genetics. 78(6). 1075–1080. 202 indexed citations
14.
Angle, Brad, et al.. (2002). Partial duplication 4q and deletion 1p36 in monozygotic twins with discordant phenotypes. American Journal of Medical Genetics. 111(3). 307–312. 5 indexed citations
15.
Angle, Brad, et al.. (2000). Case of partial duplication 2q3 with characteristic phenotype: Rare occurrence of an unbalanced offspring resulting from a parental pericentric inversion. American Journal of Medical Genetics. 91(2). 126–130. 21 indexed citations
16.
Angle, Brad, et al.. (1999). Case of partial trisomy 9p and partial trisomy 14q resulting from a maternal translocation: Overlapping manifestations of characteristic phenotypes. American Journal of Medical Genetics. 84(2). 132–136. 15 indexed citations
17.
Angle, Brad, Joseph H. Hersh, & Katherine Christensen. (1998). Molecularly proven hypochondroplasia with cloverleaf skull deformity: a novel association. Clinical Genetics. 54(5). 417–420. 19 indexed citations
18.
Hersh, Joseph H., Brad Angle, Marcello Pietrantoni, et al.. (1998). Predictive Value of Fetal Ultrasonography in the Diagnosis of a Lethal Skeletal Dysplasia. Southern Medical Journal. 91(12). 1137–1142. 16 indexed citations
19.
Angle, Brad & Joseph H. Hersh. (1997). Anophthalmia, intracerebral cysts, and cleft lip/palate: Expansion of the phenotype in oculocerebrocutaneous syndrome?. American Journal of Medical Genetics. 68(1). 39–42. 10 indexed citations
20.
Angle, Brad, et al.. (1994). Microcephaly, lymphedema, and chorioretinal dysplasia: Report of two additional cases. American Journal of Medical Genetics. 53(2). 99–101. 13 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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