Kira Apse

2.1k total citations
16 papers, 798 citations indexed

About

Kira Apse is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Kira Apse has authored 16 papers receiving a total of 798 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Pediatrics, Perinatology and Child Health, 7 papers in Genetics and 5 papers in Molecular Biology. Recurrent topics in Kira Apse's work include Fetal and Pediatric Neurological Disorders (6 papers), BRCA gene mutations in cancer (3 papers) and Genomics and Rare Diseases (2 papers). Kira Apse is often cited by papers focused on Fetal and Pediatric Neurological Disorders (6 papers), BRCA gene mutations in cancer (3 papers) and Genomics and Rare Diseases (2 papers). Kira Apse collaborates with scholars based in United States, Türkiye and France. Kira Apse's co-authors include Jiongdong Pang, Robert C. Stanton, Zhiquan Zhang, Mark D. Rose, Wang-Ni Tian, Bernard S. Chang, Christopher A. Walsh, Christopher A. Walsh, Barbara B. Biesecker and Volney Sheen and has published in prestigious journals such as Journal of Biological Chemistry, Neurology and American Journal of Public Health.

In The Last Decade

Kira Apse

15 papers receiving 771 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kira Apse United States	12	261	215	208	126	83	16	798
Luísa Diogo Portugal	20	790 3.0×	304 1.4×	143 0.7×	185 1.5×	47 0.6×	71	1.4k
Lori M. Roberts United States	7	431 1.7×	175 0.8×	171 0.8×	67 0.5×	30 0.4×	8	977
Frédérique Guénot France	3	408 1.6×	223 1.0×	111 0.5×	291 2.3×	131 1.6×	3	1.1k
Olga Stephansson Sweden	11	332 1.3×	223 1.0×	55 0.3×	129 1.0×	84 1.0×	13	768
K. Tada Japan	24	889 3.4×	145 0.7×	224 1.1×	164 1.3×	72 0.9×	102	1.6k
Mehmet Seven Türkiye	15	304 1.2×	115 0.5×	265 1.3×	62 0.5×	67 0.8×	59	765
A. A. M. Morris United Kingdom	17	613 2.3×	126 0.6×	115 0.6×	254 2.0×	55 0.7×	27	1.0k
Donald T. Whelan Canada	20	488 1.9×	243 1.1×	166 0.8×	101 0.8×	39 0.5×	42	917
Curtis R. Coughlin United States	21	774 3.0×	310 1.4×	255 1.2×	153 1.2×	50 0.6×	49	1.4k
Alex E. Felice Malta	16	270 1.0×	129 0.6×	132 0.6×	153 1.2×	29 0.3×	59	1.0k

Countries citing papers authored by Kira Apse

Since Specialization

Citations

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

Fields of papers citing papers by Kira Apse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kira Apse

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

All Works

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16 of 16 papers shown

Seifert, Wenke, Muriel Holder‐Espinasse, Jirko Kühnisch, et al.. (2008). Expanded mutational spectrum in Cohen syndrome, tissue expression, and transcript variants ofCOH1. Human Mutation. 30(2). E404–E420. 38 indexed citations

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

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

Chang, Bernard S., Seonhee Kim, Abha Aggarwal, et al.. (2006). The role of RELN in lissencephaly and neuropsychiatric disease. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 144B(1). 58–63. 47 indexed citations

Tsao, Jack W., Jason Neal, Kira Apse, et al.. (2006). Cerebellar Ataxia With Progressive Improvement. Archives of Neurology. 63(4). 594–594. 5 indexed citations

Gérard‐Blanluet, Marion, Volney Sheen, Jason Neal, et al.. (2006). Bilateral periventricular heterotopias in an X‐linked dominant transmission in a family with two affected males. American Journal of Medical Genetics Part A. 140A(10). 1041–1046. 20 indexed citations

Ferland, Russell J., John Gaitanis, Kira Apse, et al.. (2006). Periventricular nodular heterotopia and Williams syndrome. American Journal of Medical Genetics Part A. 140A(12). 1305–1311. 39 indexed citations

Neal, Jason, Kira Apse, Mustafa Şahin, Christopher A. Walsh, & Volney Sheen. (2006). Deletion of chromosome 1p36 is associated with periventricular nodular heterotopia. American Journal of Medical Genetics Part A. 140A(15). 1692–1695. 26 indexed citations

Chang, Bernard S., Kira Apse, Roberto Caraballo, et al.. (2006). A familial syndrome of unilateral polymicrogyria affecting the right hemisphere. Neurology. 66(1). 133–135. 34 indexed citations

10.

Tietjen, Ian, Füsun Ferda Erdoğan, Sophie Currier, et al.. (2005). EMX2‐independent familial schizencephaly: Clinical and genetic analyses. American Journal of Medical Genetics Part A. 135A(2). 166–170. 11 indexed citations

11.

Gollust, Sarah E., et al.. (2005). Community Involvement in Developing Policies for Genetic Testing: Assessing the Interests and Experiences of Individuals Affected by Genetic Conditions. American Journal of Public Health. 95(1). 35–41. 30 indexed citations

12.

Miller, Paul Steven, et al.. (2005). Community Involvement in Developing Policies for Genetic Testing: Assessing the Interests and Experiences of Individuals Affected by Genetic Conditions. SSRN Electronic Journal.

13.

Apse, Kira, et al.. (2004). Perceptions of genetic discrimination among at-risk relatives of colorectal cancer patients. Genetics in Medicine. 6(6). 510–516. 47 indexed citations

14.

Zhang, Zhiquan, Kira Apse, Jiongdong Pang, & Robert C. Stanton. (2001). High glucose inhibits glucose-6-phosphate dehydrogenase via cAMP in aortic endothelial cells.. Journal of Biological Chemistry. 276(7). 5412–5412. 6 indexed citations

15.

Zhang, Zhiquan, Kira Apse, Jiongdong Pang, & Robert C. Stanton. (2000). High Glucose Inhibits Glucose-6-phosphate Dehydrogenase via cAMP in Aortic Endothelial Cells. Journal of Biological Chemistry. 275(51). 40042–40047. 190 indexed citations

16.

Tian, Wang-Ni, et al.. (1999). Importance of glucose-6-phosphate dehydrogenase activity in cell death. American Journal of Physiology-Cell Physiology. 276(5). C1121–C1131. 219 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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