Jannine D. Cody

2.6k total citations
63 papers, 1.5k citations indexed

About

Jannine D. Cody is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Jannine D. Cody has authored 63 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 52 papers in Genetics, 35 papers in Molecular Biology and 18 papers in Plant Science. Recurrent topics in Jannine D. Cody's work include Genomic variations and chromosomal abnormalities (47 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Chromosomal and Genetic Variations (18 papers). Jannine D. Cody is often cited by papers focused on Genomic variations and chromosomal abnormalities (47 papers), Genetics and Neurodevelopmental Disorders (21 papers) and Chromosomal and Genetic Variations (18 papers). Jannine D. Cody collaborates with scholars based in United States, France and United Kingdom. Jannine D. Cody's co-authors include Robin J. Leach, Daniel E. Hale, Patricia Heard, Courtney Sebold, Bridgette Soileau, Frederick R. Singer, Jack L. Lancaster, Celia I. Kaye, Zoran Brkanac and Erika Carter and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Journal of Virology and The FASEB Journal.

In The Last Decade

Jannine D. Cody

61 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jannine D. Cody United States 25 971 729 312 275 222 63 1.5k
R. J. M. Gardner New Zealand 18 682 0.7× 766 1.1× 137 0.4× 356 1.3× 178 0.8× 27 1.6k
Almuth Caliebe Germany 23 678 0.7× 655 0.9× 95 0.3× 324 1.2× 96 0.4× 66 1.4k
Anna Lindstrand Sweden 22 827 0.9× 882 1.2× 140 0.4× 135 0.5× 58 0.3× 84 1.5k
Naomichi Matsumoto Japan 16 587 0.6× 525 0.7× 234 0.8× 150 0.5× 62 0.3× 26 942
Maureen Bocian United States 18 1.4k 1.5× 1.2k 1.7× 101 0.3× 241 0.9× 114 0.5× 35 2.1k
Joris Andrieux France 23 1.2k 1.3× 1.1k 1.5× 203 0.7× 266 1.0× 98 0.4× 97 2.0k
Kwame Anyane‐Yeboa United States 26 1.2k 1.3× 1.3k 1.7× 222 0.7× 361 1.3× 97 0.4× 66 2.3k
Jean‐Pierre Fryns Belgium 18 635 0.7× 664 0.9× 82 0.3× 185 0.7× 209 0.9× 72 1.3k
Desirée du Sart Australia 26 617 0.6× 888 1.2× 373 1.2× 71 0.3× 251 1.1× 39 2.0k
Ann‐Charlotte Thuresson Sweden 20 485 0.5× 655 0.9× 77 0.2× 97 0.4× 42 0.2× 34 1.1k

Countries citing papers authored by Jannine D. Cody

Since Specialization
Citations

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

Fields of papers citing papers by Jannine D. Cody

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jannine D. Cody. 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 Jannine D. Cody. The network helps show where Jannine D. Cody may publish in the future.

Co-authorship network of co-authors of Jannine D. Cody

This figure shows the co-authorship network connecting the top 25 collaborators of Jannine D. Cody. A scholar is included among the top collaborators of Jannine D. Cody 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 Jannine D. Cody. Jannine D. Cody 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.
Gelfond, Jonathan, et al.. (2023). Causes of death in individuals with trisomy 18 after the first year of life. American Journal of Medical Genetics Part A. 194(2). 279–287. 3 indexed citations
2.
Cody, Jannine D.. (2020). The Consequences of Abnormal Gene Dosage: Lessons from Chromosome 18. Trends in Genetics. 36(10). 764–776. 5 indexed citations
3.
Sebold, Courtney, Patricia Heard, Erika Carter, et al.. (2015). A review of 18p deletions. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 169(3). 251–264. 57 indexed citations
4.
Perry, Brian P. & Jannine D. Cody. (2014). Otologic characteristics of individuals with deletions of distal 18q. The Laryngoscope. 124(11). 2606–2609. 4 indexed citations
5.
Hermetz, Karen, Scott Newman, Karen N. Conneely, et al.. (2014). Large Inverted Duplications in the Human Genome Form via a Fold-Back Mechanism. PLoS Genetics. 10(1). e1004139–e1004139. 54 indexed citations
6.
Hermetz, Karen, Urvashi Surti, Jannine D. Cody, & M. Katharine Rudd. (2012). A recurrent translocation is mediated by homologous recombination between HERV-H elements. Molecular Cytogenetics. 5(1). 6–6. 18 indexed citations
7.
Luo, Yue, Karen Hermetz, Jennifer G. Mullé, et al.. (2011). Diverse mutational mechanisms cause pathogenic subtelomeric rearrangements. Human Molecular Genetics. 20(19). 3769–3778. 31 indexed citations
8.
Sebold, Courtney, Elizabeth Roeder, Bridgette Soileau, et al.. (2010). Tetrasomy 18p: Report of the molecular and clinical findings of 43 individuals. American Journal of Medical Genetics Part A. 152A(9). 2164–2172. 50 indexed citations
9.
Medina, Rolando, Patricia Heard, Erika Carter, et al.. (2009). Psychiatric syndromes in individuals with chromosome 18 abnormalities. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 153B(3). 837–845. 10 indexed citations
10.
Heard, Patricia, et al.. (2009). High resolution genomic analysis of 18q− using oligo‐microarray comparative genomic hybridization (aCGH). American Journal of Medical Genetics Part A. 149A(7). 1431–1437. 42 indexed citations
11.
Horbinski, Craig, Patricia Heard, Malini Sathanoori, et al.. (2008). Molecular and clinical characterization of a recurrent cryptic unbalanced t(4q;18q) resulting in an 18q deletion and 4q duplication. American Journal of Medical Genetics Part A. 146A(22). 2898–2904. 18 indexed citations
12.
Cody, Jannine D.. (2006). Creating partnerships and improving health care: The role of genetic advocacy groups. Genetics in Medicine. 8(12). 797–799. 7 indexed citations
13.
Baillargeon, Jacques, et al.. (2002). Molecular characterization of 18p deletions: Evidence for a breakpoint cluster. Genetics in Medicine. 4(1). 15–19. 26 indexed citations
14.
Lehman, Donna M., W.E. Sponsel, Robert F. Stratton, et al.. (2001). Genetic mapping of a novel X-linked recessive colobomatous microphthalmia. American Journal of Medical Genetics. 101(2). 114–119. 16 indexed citations
15.
Cody, Jannine D., et al.. (1999). Gene expression patterns in cell lines from patients with 18q- syndrome. Human Genetics. 104(6). 467–475. 24 indexed citations
16.
Cody, Jannine D., et al.. (1999). Haplosufficiency of the melanocortin-4 receptor gene in individuals with deletions of 18q. Human Genetics. 105(5). 424–427. 23 indexed citations
17.
Cody, Jannine D., Zoran Brkanac, Rosemarie Plaetke, et al.. (1997). Preferential loss of the paternal alleles in the 18q- syndrome. American Journal of Medical Genetics. 69(3). 280–286. 65 indexed citations
18.
Cody, Jannine D., Daniel E. Hale, Zoran Brkanac, Celia I. Kaye, & Robin J. Leach. (1997). Growth hormone insufficiency associated with haploinsufficiency at 18q23. American Journal of Medical Genetics. 71(4). 420–425. 45 indexed citations
19.
Cody, Jannine D., Frederick R. Singer, G. David Roodman, et al.. (1997). Genetic Linkage of Paget Disease of the Bone to Chromosome 18q. The American Journal of Human Genetics. 61(5). 1117–1122. 122 indexed citations
20.
Ghidoni, Patricia D., et al.. (1994). Growth hormone deficiency in 18q deletion syndrome. The American Journal of Human Genetics. 55. 1 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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