Devon Lamb Thrush

1.1k total citations
19 papers, 334 citations indexed

About

Devon Lamb Thrush is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Devon Lamb Thrush has authored 19 papers receiving a total of 334 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Devon Lamb Thrush's work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (4 papers) and Prenatal Screening and Diagnostics (4 papers). Devon Lamb Thrush is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (4 papers) and Prenatal Screening and Diagnostics (4 papers). Devon Lamb Thrush collaborates with scholars based in United States and United Kingdom. Devon Lamb Thrush's co-authors include Julie M. Gastier‐Foster, Caroline Astbury, Robert E. Pyatt, Shalini C. Reshmi, Sayaka Hashimoto, C M Wiles, David H. Miller, N. Alsanjari, A. E. Harding and F Scaravilli and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of the American College of Cardiology and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Devon Lamb Thrush

19 papers receiving 312 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Devon Lamb Thrush United States 10 218 141 54 29 27 19 334
Sandra Whalen France 13 268 1.2× 157 1.1× 59 1.1× 17 0.6× 24 0.9× 28 417
Tuva Barøy Norway 12 221 1.0× 161 1.1× 44 0.8× 29 1.0× 9 0.3× 21 333
Angelien Heister Netherlands 10 227 1.0× 69 0.5× 42 0.8× 20 0.7× 30 1.1× 10 437
Adeline Ngoh United Kingdom 8 136 0.6× 175 1.2× 69 1.3× 28 1.0× 11 0.4× 15 367
Jens Schallner Germany 11 182 0.8× 120 0.9× 50 0.9× 10 0.3× 34 1.3× 15 324
Michele Iacomino Italy 11 169 0.8× 108 0.8× 106 2.0× 12 0.4× 16 0.6× 35 382
Clara DM van Karnebeek Canada 7 190 0.9× 105 0.7× 49 0.9× 78 2.7× 9 0.3× 7 349
Valeria Cinquina Italy 11 112 0.5× 193 1.4× 40 0.7× 9 0.3× 27 1.0× 22 388
Dimitar N. Azmanov Australia 12 191 0.9× 122 0.9× 75 1.4× 26 0.9× 7 0.3× 23 336

Countries citing papers authored by Devon Lamb Thrush

Since Specialization
Citations

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

Fields of papers citing papers by Devon Lamb Thrush

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Devon Lamb Thrush. 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 Devon Lamb Thrush. The network helps show where Devon Lamb Thrush may publish in the future.

Co-authorship network of co-authors of Devon Lamb Thrush

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

All Works

19 of 19 papers shown
1.
Hagman, Kelly D. Farwell, et al.. (2020). Facing the challenge of genetic counselors' need for rapid continuing education about genomic technologies. Journal of Genetic Counseling. 29(5). 838–848. 5 indexed citations
2.
Darabi, Sourat, et al.. (2019). Clinical validity assessment of genes for inclusion in multi‐gene panel testing: A systematic approach. Molecular Genetics & Genomic Medicine. 7(5). e630–e630. 4 indexed citations
3.
Powis, Zöe, Devon Lamb Thrush, Brigette Tippin Davis, & Jill S. Dolinsky. (2016). DIAGNOSTIC EXOME SEQUENCING IN PEDIATRIC PATIENTS WITH CONGENITAL HEART DISEASE. Journal of the American College of Cardiology. 67(13). 991–991. 3 indexed citations
4.
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
5.
Hashimoto, Sayaka, Devon Lamb Thrush, Shalini C. Reshmi, et al.. (2014). Variability in pathogenicity prediction programs: impact on clinical diagnostics. Molecular Genetics & Genomic Medicine. 3(2). 99–110. 39 indexed citations
6.
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
7.
Pfau, Ruthann, Devon Lamb Thrush, Dennis Bartholomew, et al.. (2013). MCPH1 deletion in a newborn with severe microcephaly and premature chromosome condensation. European Journal of Medical Genetics. 56(11). 609–613. 9 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.
Hickey, Scott E., Devon Lamb Thrush, Shalini C. Reshmi, et al.. (2013). A case of an atypically large proximal 15q deletion as cause for Prader–Willi syndrome arising from a de novo unbalanced translocation. European Journal of Medical Genetics. 56(9). 510–514. 3 indexed citations
10.
Bowden, Sasigarn A., et al.. (2013). Autosomal Dominant Pseudohypoaldosteronism Type 1 in an Infant with Salt Wasting Crisis Associated with Urinary Tract Infection and Obstructive Uropathy. SHILAP Revista de lepidopterología. 2013. 1–5. 16 indexed citations
11.
Hickey, Scott E., Sawona Biswas, Devon Lamb Thrush, et al.. (2013). Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion. European Journal of Medical Genetics. 56(9). 521–525. 1 indexed citations
12.
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
13.
Repnikova, Elena, Caroline Astbury, Shalini C. Reshmi, et al.. (2012). Microarray comparative genomic hybridization and cytogenetic characterization of tissue‐specific mosaicism in three patients. American Journal of Medical Genetics Part A. 158A(8). 1924–1933. 17 indexed citations
14.
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
15.
Cottrell, Catherine E., Natalie Bir, Liz Varga, et al.. (2011). Contactin 4 as an autism susceptibility locus. Autism Research. 4(3). 189–199. 46 indexed citations
16.
Rosales, Xiomara Q., Julie M. Gastier‐Foster, Sarah Lewis, et al.. (2010). Novel diagnostic features of dysferlinopathies. Muscle & Nerve. 42(1). 14–21. 59 indexed citations
17.
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
18.
Harding, Brian, N. Alsanjari, Sarah Smith, et al.. (1995). Progressive neuronal degeneration of childhood with liver disease (Alpers' disease) presenting in young adults.. Journal of Neurology Neurosurgery & Psychiatry. 58(3). 320–325. 54 indexed citations
19.
Thrush, Devon Lamb, et al.. (1987). X-linked bulbo-spinal neuronopathy: a family study of three patients.. Journal of Neurology Neurosurgery & Psychiatry. 50(3). 279–284. 27 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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