Brad Angle

2.6k citations

33 papers · 1000 indexed · h-index 18

Impact in

Genetics top 5%
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
Clinical Biochemistry top 5%
- Metabolism and Genetic Disorders

Papers in ⓘ

Genetics 18
- Genomic variations and chromosomal abnormalities 9
- Connective tissue disorders research 3
- Genetics and Neurodevelopmental Disorders 3
Developmental Biology 1

Co-authors: Barbara K. Burton (8 shared papers)Katherine H. Kim (1 shared paper)Vishwanathan Hucthagowder (1 shared paper)Lihua Y. Marmorstein (1 shared paper)Nina Sausgruber (1 shared paper)Zsolt Urbán (1 shared paper)Laurence I. Burd (1 shared paper)Joseph H. Hersh (10 shared papers)
Journals: Molecular Genetics and Metabolism (2 papers)Genetics in Medicine (2 papers)Prenatal Diagnosis (2 papers)American Journal of Medical Genetics (12 papers)Birth Defects Research Part A Clinical and Molecular Teratology (1 paper)
Partner nations: United States Germany Poland

In The Last Decade

Brad Angle

32 papers receiving 975 citations

Peers

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-authors

The 25 scholars most cited alongside Brad Angle, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Brad Angle Line = papers co-authored together Brad Angle links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Fibulin-4: A Novel Gene for an Autosomal Recessive Cutis Laxa Syndrome The American Journal of Human Genetics ·Vishwanathan Hucthagowder, Nina Sausgruber, Katherine H. Kim, Brad Angle, Lihua Y. Marmorstein, Zsolt Urbán	2006	202
2	An increased incidence of haemangiomas in infants born following chorionic villus sampling (CVS) Prenatal Diagnosis ·Barbara K. Burton, Charlene J. Schulz, Brad Angle, Laurence I. Burd	1995	122
3	Mutations in PPIB (cyclophilin B) delay type I procollagen chain association and result in perinatal lethal to moderate osteogenesis imperfecta phenotypes Human Molecular Genetics ·Shawna M. Pyott, Ulrike Schwarze, Helena E. Christiansen, Melanie Pepin, Dru F. Leistritz, Richard Dineen, Catharine Harris, Barbara K. Burton, Brad Angle, Katherine Kim, Michael D. Sussman, MaryAnn Weis, David R. Eyre, David W. Russell, Kevin McCarthy, Robert D. Steiner, Peter H. Byers	2011	89
4	Whole exome sequence analysis of Peters anomaly Human Genetics ·Eric Weh, Linda M. Reis, Hannah C. Happ, Alex V. Levin, Patricia G. Wheeler, Karen L. David, Erin Carney, Brad Angle, Natalie Hauser, Elena V. Semina	2014	53
5	Risk of sudden death and acute life-threatening events in patients with glutaric acidemia type II Molecular Genetics and Metabolism ·Brad Angle, Barbara K. Burton	2007	46
6	Neonatal progeroid (Wiedemann-Rautenstrauch) syndrome: Report of five new cases and review American Journal of Medical Genetics ·Enik K rm n Pivnick, Brad Angle, Robert A. Kaufman, Bryan D. Hall, Pisit Pitukcheewanont, Joseph H. Hersh, John L. Fowlkes, Lynda P. Sanders, John M. O’Brien, Gregory S. Carroll, Wendy M. Gunther, Helen G. Morrow, George A. Burghen, Jewell C. Ward	2000	45
7	Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder American Journal of Medical Genetics Part A ·Francisca Millan, Megan T. Cho, Kyle Retterer, Kristin G. Monaghan, Renkui Bai, Patrik Vitazka, David B. Everman, Brooke Smith, Brad Angle, Victoria H. J. Roberts, LaDonna Immken, Honey Nagakura, Marc DiFazio, Elliott H. Sherr, Eden Haverfield, Bethany Friedman, Aida Telegrafi, Jane Juusola, Wendy K. Chung, Sherri J. Bale	2016	42
8	Further Evidence of Contrasting Phenotypes Caused by Reciprocal Deletions and Duplications: Duplication of NSD1 Causes Growth Retardation and Microcephaly Molecular Syndromology ·Jill A. Rosenfeld, Kyae Hyung Kim, Brad Angle, Robin Troxell, Jerome L. Gorski, Maggie Westemeyer, Moshe Frydman, Y. Senturias, Dawn Earl, Beth S. Torchia, Roger A. Schultz, Jay W. Ellison, Karen D. Tsuchiya, Sarah Zimmerman, Teresa A. Smolarek, B. C. Ballif, L.G. Shaffer	2012	37
9	Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiency Genetics in Medicine ·Devin Oglesbee, Miao He, Nilanjana Majumder, Jerry Vockley, Ayesha Ahmad, Brad Angle, Barbara K. Burton, Joel Charrow, Regina Ensenauer, Can Fıçıcıoğlu, Laura Davis Keppen, Deborah Marsden, Silvia Tortorelli, Si Houn Hahn, Dietrich Matern	2007	33
10	Distinctive phenotype in 9 patients with deletion of chromosome 1q24‐q25 American Journal of Medical Genetics Part A ·Deepika Burkardt, Jill A. Rosenfeld, Maria Helgeson, Brad Angle, Valerie Banks, Wendy E. Smith, Karen W. Gripp, Jessica Moline, Rocio Moran, Dmitriy M. Niyazov, Cathy A. Stevens, Elaine H. Zackai, Robert Roger Lebel, Douglas G. Ashley, Nancy Kramer, Ralph S. Lachman, John M. Graham	2011	29
11	Evaluation and classification of severity for 176 genes on an expanded carrier screening panel Prenatal Diagnosis ·Aishwarya Arjunan, Holly Bellerose, Raúl Torres, Rotem Ben‐Shachar, Jodi D. Hoffman, Brad Angle, Robert Nathan Slotnick, Brittany Simpson, Andrea M. Lewis, Pilar Magoulas, Kelly Bontempo, Jeanine Schulze, Jennifer Tarpinian, Jessica Bucher, Richard Dineen, Allison L. Goetsch, Gabriel A. Lazarin, Katherine Johansen Taber	2020	28
12	Early‐life epileptic encephalopathy secondary to SZT2 pathogenic recessive variants Epileptic Disorders ·Charu Venkatesan, Brad Angle, J Gordon Millichap	2016	28
13	A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects Neurogenetics ·David B. Beck, Megan T. Cho, Francisca Millan, Carin Yates, Mark Hannibal, Bridget O’Connor, Marwan Shinawi, Anne M. Connolly, Darrel Waggoner, Sara Halbach, Brad Angle, Victoria R. Sanders, Yufeng Shen, Kyle Retterer, Amber Begtrup, Renkui Bai, Wendy K. Chung	2016	25
14	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 ·Loren Peña, Brad Angle, Barbara K. Burton, Joel Charrow	2012	22
15	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 ·Brad Angle, Joseph H. Hersh, Frank Yen, Katherine Christensen	2000	21
16	Molecularly proven hypochondroplasia with cloverleaf skull deformity: a novel association Clinical Genetics ·Brad Angle, Joseph H. Hersh, Katherine Christensen	1998	19
17	Atypical case of Smith-Lemli-Opitz syndrome: Implications for diagnosis American Journal of Medical Genetics ·Brad Angle, G S Tint, Oraib A. Yacoub, Ann L. Clark	1998	19
18	Further delineation of Aymé‐Gripp syndrome and use of automated facial analysis tool American Journal of Medical Genetics Part A ·Shivarajan Amudhavalli, Randi Hanson, Brad Angle, Kelly Bontempo, Karen W. Gripp	2018	17
19	Predictive Value of Fetal Ultrasonography in the Diagnosis of a Lethal Skeletal Dysplasia Southern Medical Journal ·Joseph H. Hersh, Brad Angle, Marcello Pietrantoni, Vernon D. Cook, Joseph A. Spinnato, Ann L. Clark, James Kurtzman, Robert W. Bendon, A Gerassimides	1998	16
20	A Pilot Newborn Screening Program for Lysosomal Storage Disorders (LSD) in Illinois Molecular Genetics and Metabolism ·Barbara K. Burton, Joel Charrow, Brad Angle, Shanna Widera, Darrel Waggoner	2012	16

About Brad Angle

Brad Angle is a scholar working on Genetics, Developmental Biology, Clinical Biochemistry, Pediatrics, Perinatology and Child Health and Molecular Biology, having authored 33 papers that have together received 1000 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (7 papers), Chromosomal and Genetic Variations (4 papers), RNA modifications and cancer (4 papers), Metabolism and Genetic Disorders (3 papers), Connective tissue disorders research (3 papers), RNA Research and Splicing (3 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (527 citations), Clinical Biochemistry (97 citations), Developmental Biology (18 citations), Rheumatology (103 citations) and Molecular Biology (444 citations). Brad Angle has collaborated with scholars based in United States, Germany and Poland. Frequent co-authors include Barbara K. Burton, Katherine H. Kim, Vishwanathan Hucthagowder, Lihua Y. Marmorstein, Nina Sausgruber, Zsolt Urbán, Laurence I. Burd, Joseph H. Hersh, Katherine Christensen and Joel Charrow. Their work appears in journals such as Molecular Genetics and Metabolism, Genetics in Medicine, Prenatal Diagnosis, American Journal of Medical Genetics and Birth Defects Research Part A Clinical and Molecular Teratology.

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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