Robert E. Pyatt

2.4k total citations
40 papers, 988 citations indexed

About

Robert E. Pyatt is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Robert E. Pyatt has authored 40 papers receiving a total of 988 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 20 papers in Molecular Biology and 7 papers in Hematology. Recurrent topics in Robert E. Pyatt's work include Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (8 papers) and Prenatal Screening and Diagnostics (6 papers). Robert E. Pyatt is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genomics and Rare Diseases (8 papers) and Prenatal Screening and Diagnostics (6 papers). Robert E. Pyatt collaborates with scholars based in United States, Nigeria and South Sudan. Robert E. Pyatt's co-authors include Thomas W. Prior, Susan Rice, Edward F. Srour, Jon McMahel, André Gothot, Sayaka Hashimoto, David Mihal, Caroline Astbury, Shalini C. Reshmi and Julie M. Gastier‐Foster and has published in prestigious journals such as Blood, American Journal Of Pathology and Clinical Chemistry.

In The Last Decade

Robert E. Pyatt

40 papers receiving 950 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Robert E. Pyatt United States 15 496 313 223 198 166 40 988
David George United States 20 697 1.4× 189 0.6× 119 0.5× 176 0.9× 94 0.6× 28 1.2k
Lilian Bomme Ousager Denmark 17 428 0.9× 114 0.4× 420 1.9× 98 0.5× 186 1.1× 57 1.1k
Roger A. Fleischman United States 17 558 1.1× 256 0.8× 272 1.2× 275 1.4× 92 0.6× 29 1.2k
Adele Giampaolo Italy 21 857 1.7× 288 0.9× 231 1.0× 491 2.5× 63 0.4× 47 1.6k
J.J. Cassiman Belgium 21 395 0.8× 348 1.1× 383 1.7× 235 1.2× 83 0.5× 56 1.4k
Helen Parker United Kingdom 23 492 1.0× 404 1.3× 198 0.9× 296 1.5× 31 0.2× 48 1.3k
I. Maric United States 12 228 0.5× 197 0.6× 66 0.3× 207 1.0× 79 0.5× 15 903
Paolo Simi Italy 22 633 1.3× 127 0.4× 571 2.6× 60 0.3× 145 0.9× 82 1.4k
Karin Pike‐Overzet Netherlands 20 623 1.3× 148 0.5× 304 1.4× 213 1.1× 42 0.3× 45 1.3k
Nuray Akyüz Germany 15 328 0.7× 136 0.4× 107 0.5× 86 0.4× 70 0.4× 53 802

Countries citing papers authored by Robert E. Pyatt

Since Specialization
Citations

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

Fields of papers citing papers by Robert E. Pyatt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Robert E. Pyatt. 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 Robert E. Pyatt. The network helps show where Robert E. Pyatt may publish in the future.

Co-authorship network of co-authors of Robert E. Pyatt

This figure shows the co-authorship network connecting the top 25 collaborators of Robert E. Pyatt. A scholar is included among the top collaborators of Robert E. Pyatt 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 Robert E. Pyatt. Robert E. Pyatt 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.
Cherukuri, Praveen F., David E. Condon, Shaopeng Gu, et al.. (2022). Establishing analytical validity of BeadChip array genotype data by comparison to whole-genome sequence and standard benchmark datasets. BMC Medical Genomics. 15(1). 56–56. 5 indexed citations
2.
Repnikova, Elena, Dmitry Lyalin, Kimberly S. McDonald, et al.. (2019). CNTN6 copy number variations: Uncertain clinical significance in individuals with neurodevelopmental disorders. European Journal of Medical Genetics. 63(1). 103636–103636. 5 indexed citations
3.
Barrie, Elizabeth S., Li Yu, Sayaka Hashimoto, et al.. (2018). Pericentromeric regions of homozygosity on the X chromosome: Another likely benign population variant. European Journal of Medical Genetics. 61(7). 416–420. 1 indexed citations
4.
Hashimoto, Sayaka, et al.. (2017). Partial tetrasomy 11q resulting from an intrachromosomal triplication of a 22 Mb region of chromosome 11. American Journal of Medical Genetics Part A. 173(4). 1056–1060. 2 indexed citations
5.
Thrush, Devon Lamb, Scott E. Hickey, Sayaka Hashimoto, et al.. (2014). Atypical breakpoint in a t(6;17) translocation case of acampomelic campomelic dysplasia. European Journal of Medical Genetics. 57(7). 315–318. 6 indexed citations
6.
Bowling, Bethany Vice, et al.. (2014). Bringing Next-Generation Sequencing into the Classroom through a Comparison of Molecular Biology Techniques. The American Biology Teacher. 76(6). 396–401. 5 indexed citations
7.
Hickey, Scott E., Theresa Mihalic Mosher, Ruthann Pfau, et al.. (2013). Duplication of the Xq27.3–q28 region, including the FMR1 gene, in an X‐linked hypogonadism, gynecomastia, intellectual disability, short stature, and obesity syndrome. American Journal of Medical Genetics Part A. 161(9). 2294–2299. 17 indexed citations
8.
Pastore, Matthew, Sayaka Hashimoto, Devon Lamb Thrush, et al.. (2013). Neurodevelopmental disorders among individuals with duplication of 4p13 to 4p12 containing a GABAA receptor subunit gene cluster. European Journal of Human Genetics. 22(1). 105–109. 14 indexed citations
9.
Repnikova, Elena, Jill A. Rosenfeld, Aimee McKinney, et al.. (2013). Characterization of copy number variation in genomic regions containing STR loci using array comparative genomic hybridization. Forensic Science International Genetics. 7(5). 475–481. 6 indexed citations
10.
Pyatt, Robert E., Aimee McKinney, Caroline Astbury, et al.. (2012). 12q14 microdeletion associated with HMGA2 gene disruption and growth restriction. American Journal of Medical Genetics Part A. 158A(11). 2925–2930. 16 indexed citations
11.
Flanigan, Kevin M., Julie M. Gastier‐Foster, Robert E. Pyatt, et al.. (2012). D.P.4 Comparison of commercially-available exome capture kits in the diagnosis of neuromuscular disorders. Neuromuscular Disorders. 22(9-10). 808–808. 1 indexed citations
12.
Kalman, Lisa V., Jay Leonard, Norman P. Gerry, et al.. (2011). Quality Assurance for Duchenne and Becker Muscular Dystrophy Genetic Testing. Journal of Molecular Diagnostics. 13(2). 167–174. 18 indexed citations
13.
Cottrell, Catherine E., Thomas W. Prior, Robert E. Pyatt, et al.. (2010). Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization. American Journal of Medical Genetics Part A. 152A(9). 2301–2307. 8 indexed citations
14.
Prior, Thomas W., Pamela J. Snyder, B Rink, et al.. (2010). Newborn and carrier screening for spinal muscular atrophy. American Journal of Medical Genetics Part A. 152A(7). 1608–1616. 193 indexed citations
15.
Carroll, Andrew J., Nyla A. Heerema, Julie M. Gastier‐Foster, et al.. (2009). Masked Hypodiploidy: Hypodiploid Acute Lymphoblastic Leukemia (ALL) in Children Mimicking Hyperdiploid ALL: A Report From the Children's Oncology Group (COG) AALL03B1 Study.. Blood. 114(22). 1580–1580. 7 indexed citations
16.
Pyatt, Robert E. & Thomas W. Prior. (2006). A feasibility study for the newborn screening of spinal muscular atrophy. Genetics in Medicine. 8(7). 428–437. 28 indexed citations
17.
Holtzclaw, J. David, Robert E. Pyatt, J. Joseph Hoey, et al.. (2005). FIRST: A Model for Developing New Science Faculty.. The journal of college science teaching. 34(6). 24–29. 12 indexed citations
18.
Kerstann, Kimberly F., Eleanor Feingold, Sallie B. Freeman, et al.. (2004). Linkage disequilibrium mapping in trisomic populations: Analytical approaches and an application to congenital heart defects in Down syndrome. Genetic Epidemiology. 27(3). 240–251. 14 indexed citations
19.
Pyatt, Robert E., et al.. (1999). Use of Merocyanine 540 for the Isolation of Quiescent, Primitive Human Bone Marrow Hematopoietic Progenitor Cells. Journal of Hematotherapy. 8(2). 189–198. 2 indexed citations
20.

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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