Adria Bodell

4.2k total citations
21 papers, 2.3k citations indexed

About

Adria Bodell is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Adria Bodell has authored 21 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 10 papers in Pediatrics, Perinatology and Child Health and 9 papers in Genetics. Recurrent topics in Adria Bodell's work include Fetal and Pediatric Neurological Disorders (10 papers), Congenital heart defects research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Adria Bodell is often cited by papers focused on Fetal and Pediatric Neurological Disorders (10 papers), Congenital heart defects research (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Adria Bodell collaborates with scholars based in United States, Israel and Türkiye. Adria Bodell's co-authors include Christopher A. Walsh, Bernard S. Chang, Meral Topçu, A. James Barkovich, Robert Hill, Yin Yao Shugart, Vijay Ganesh, R. Sean Hill, Rachel Straussberg and Lina Basel‐Vanagaite and has published in prestigious journals such as Science, Neuron and Nature Genetics.

In The Last Decade

Adria Bodell

21 papers receiving 2.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adria Bodell United States 19 1.2k 733 729 586 379 21 2.3k
Meral Topçu Türkiye 24 1.4k 1.2× 718 1.0× 399 0.5× 509 0.9× 306 0.8× 85 2.5k
Christopher A. Walsh United States 21 659 0.6× 534 0.7× 676 0.9× 755 1.3× 268 0.7× 31 1.8k
Karine Poirier France 23 1.2k 1.0× 778 1.1× 414 0.6× 370 0.6× 698 1.8× 48 2.1k
R. Sean Hill United States 13 956 0.8× 624 0.9× 286 0.4× 267 0.5× 199 0.5× 17 1.7k
Sharon Minnerath United States 15 989 0.8× 353 0.5× 820 1.1× 240 0.4× 307 0.8× 17 1.9k
Matthew R. Sarkisian United States 32 1.7k 1.4× 780 1.1× 1.1k 1.5× 545 0.9× 397 1.0× 63 3.5k
Elena Parrini Italy 22 899 0.8× 1.0k 1.4× 549 0.8× 596 1.0× 227 0.6× 61 2.2k
Yaman Z. Ekşioğlu United States 16 529 0.5× 313 0.4× 480 0.7× 413 0.7× 236 0.6× 23 1.5k
Chérif Beldjord France 30 2.5k 2.1× 1.3k 1.8× 686 0.9× 453 0.8× 698 1.8× 59 4.3k
Carlos Cardoso France 24 1.2k 1.0× 871 1.2× 302 0.4× 282 0.5× 286 0.8× 37 2.0k

Countries citing papers authored by Adria Bodell

Since Specialization
Citations

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

Fields of papers citing papers by Adria Bodell

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adria Bodell

This figure shows the co-authorship network connecting the top 25 collaborators of Adria Bodell. A scholar is included among the top collaborators of Adria Bodell 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 Adria Bodell. Adria Bodell 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.
Dies, Kira A., Adria Bodell, Fuki M. Hisama, et al.. (2012). Schizencephaly. Journal of Child Neurology. 28(2). 198–203. 21 indexed citations
2.
Shen, Jun, Edward C. Gilmore, Mary Haddadin, et al.. (2010). Mutations in PNKP cause microcephaly, seizures and defects in DNA repair. Nature Genetics. 42(3). 245–249. 213 indexed citations
3.
Mochida, Ganeshwaran H., Muhammad Mahajnah, Anthony D. Hill, et al.. (2009). A Truncating Mutation of TRAPPC9 Is Associated with Autosomal-Recessive Intellectual Disability and Postnatal Microcephaly. The American Journal of Human Genetics. 85(6). 897–902. 107 indexed citations
4.
Hill, Anthony D., Bernard S. Chang, Robert Hill, et al.. (2007). A 2‐Mb critical region implicated in the microcephaly associated with terminal 1q deletion syndrome. American Journal of Medical Genetics Part A. 143A(15). 1692–1698. 52 indexed citations
5.
Tietjen, Ian, Adria Bodell, Kira Apse, et al.. (2007). Comprehensive EMX2 genotyping of a large schizencephaly case series. American Journal of Medical Genetics Part A. 143A(12). 1313–1316. 30 indexed citations
6.
Chang, Bernard S., Tami Katzir, Tong Liu, et al.. (2007). A structural basis for reading fluency: White matter defects in a genetic brain malformation. Neurology. 69(23). 2146–2154. 56 indexed citations
7.
Rajab, Anna, et al.. (2006). An autosomal recessive form of spastic cerebral palsy (CP) with microcephaly and mental retardation. American Journal of Medical Genetics Part A. 140A(14). 1504–1510. 17 indexed citations
8.
Masruha, Marcelo Rodrigues, Luís Otávio Sales Ferreira Caboclo, Henrique Carrete, et al.. (2006). Mutation in Filamin A Causes Periventricular Heterotopia, Developmental Regression, and West Syndrome in Males. Epilepsia. 47(1). 211–214. 18 indexed citations
9.
Currier, Sophie, Christine K. Lee, Bernard S. Chang, et al.. (2005). Mutations inPOMT1 are found in a minority of patients with Walker-Warburg syndrome. American Journal of Medical Genetics Part A. 133A(1). 53–57. 43 indexed citations
10.
Piao, Xianhua, Bernard S. Chang, Adria Bodell, et al.. (2005). Genotype–phenotype analysis of human frontoparietal polymicrogyria syndromes. Annals of Neurology. 58(5). 680–687. 103 indexed citations
11.
Piao, Xianhua, R. Sean Hill, Adria Bodell, et al.. (2004). G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex. Science. 303(5666). 2033–2036. 405 indexed citations
12.
Ferland, Russell J., Wafaa Eyaid, Randall V. Collura, et al.. (2004). Abnormal cerebellar development and axonal decussation due to mutations in AHI1 in Joubert syndrome. Nature Genetics. 36(9). 1008–1013. 286 indexed citations
13.
Chang, Bernard S., Xianhua Piao, G. D. Cascino, et al.. (2004). Bilateral generalized polymicrogyria (BGP). Neurology. 62(10). 1722–1728. 44 indexed citations
14.
Chang, Bernard S., Xianhua Piao, Adria Bodell, et al.. (2003). Bilateral frontoparietal polymicrogyria: Clinical and radiological features in 10 families with linkage to chromosome 16. Annals of Neurology. 53(5). 596–606. 100 indexed citations
15.
Sheen, Volney, Vijay Ganesh, Meral Topçu, et al.. (2003). Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex. Nature Genetics. 36(1). 69–76. 273 indexed citations
16.
Sheen, Volney, Lina Basel‐Vanagaite, Jean R. Goodman, et al.. (2003). Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus. Brain and Development. 26(5). 326–334. 41 indexed citations
17.
Sheen, Volney, James W. Wheless, Adria Bodell, et al.. (2003). Periventricular heterotopia associated with chromosome 5p anomalies. Neurology. 60(6). 1033–1036. 76 indexed citations
18.
Sheen, Volney, Meral Topçu, Samuel F. Berkovic, et al.. (2003). Autosomal recessive form of periventricular heterotopia. Neurology. 60(7). 1108–1112. 48 indexed citations
19.
Warner, Laura E., Max J. Hilz, Stanley H. Appel, et al.. (1996). Clinical Phenotypes of Different MPZ (P0) Mutations May Include Charcot–Marie–Tooth Type 1B, Dejerine–Sottas, and Congenital Hypomyelination. Neuron. 17(3). 451–460. 288 indexed citations
20.
Shohat, Mordechai, Ralph Lachman, Helen E. Gruber, et al.. (1994). Desbuquois syndrome: Clinical, radiographic, and morphologic characterization. American Journal of Medical Genetics. 52(1). 9–18. 30 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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