Yonit A. Addissie

749 total citations
11 papers, 144 citations indexed

About

Yonit A. Addissie is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Yonit A. Addissie has authored 11 papers receiving a total of 144 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Yonit A. Addissie's work include Genetic Syndromes and Imprinting (2 papers), Craniofacial Disorders and Treatments (2 papers) and Cleft Lip and Palate Research (2 papers). Yonit A. Addissie is often cited by papers focused on Genetic Syndromes and Imprinting (2 papers), Craniofacial Disorders and Treatments (2 papers) and Cleft Lip and Palate Research (2 papers). Yonit A. Addissie collaborates with scholars based in United States, Germany and Nigeria. Yonit A. Addissie's co-authors include Paul Kruszka, Maximilian Muenke, Ariel F. Martinez, Kristen Malecki, Zoë C. Wong, Joshua L. Everson, Beth A. Kozel, Robert J. Lipinski, María J. Guillen Sacoto and H. Collmann and has published in prestigious journals such as Oncogene, Scientific Reports and The Journal of Pediatrics.

In The Last Decade

Yonit A. Addissie

10 papers receiving 143 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Yonit A. Addissie United States	6	77	66	17	14	14	11	144
Tossaporn Seeherunvong United States	7	131 1.7×	113 1.7×	15 0.9×	18 1.3×	8 0.6×	14	201
H. Valdes‐Socin Belgium	8	79 1.0×	79 1.2×	9 0.5×	24 1.7×	16 1.1×	26	277
Federica Tamburrino Italy	9	102 1.3×	80 1.2×	13 0.8×	15 1.1×	13 0.9×	16	174
Annamaria Perri Italy	9	128 1.7×	128 1.9×	11 0.6×	23 1.6×	12 0.9×	17	227
Márta Czakó Hungary	11	112 1.5×	141 2.1×	30 1.8×	20 1.4×	6 0.4×	40	245
Anastasia Pepe Italy	7	55 0.7×	85 1.3×	21 1.2×	33 2.4×	19 1.4×	7	311
Thaís Kataoka Homma Brazil	10	144 1.9×	148 2.2×	34 2.0×	31 2.2×	22 1.6×	19	292
P. Pearson United States	11	48 0.6×	54 0.8×	21 1.2×	14 1.0×	13 0.9×	17	180
Sandra Batista United States	4	90 1.2×	36 0.5×	11 0.6×	6 0.4×	9 0.6×	5	180

Countries citing papers authored by Yonit A. Addissie

Since Specialization

Citations

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

Fields of papers citing papers by Yonit A. Addissie

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yonit A. Addissie. 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 Yonit A. Addissie. The network helps show where Yonit A. Addissie may publish in the future.

Co-authorship network of co-authors of Yonit A. Addissie

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

All Works

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11 of 11 papers shown

Wisniewski, David, Donna Voeller, Yonit A. Addissie, et al.. (2025). EGFR amplification and PI3K pathway mutations identify a subset of breast cancers that synergistically respond to EGFR and PI3K inhibition. Oncogene. 45(1). 15–25.

Ekure, Ekanem N., Adebowale Adeyemo, Hanhan Liu, et al.. (2021). Exome Sequencing and Congenital Heart Disease in Sub-Saharan Africa. Circulation Genomic and Precision Medicine. 14(1). e003108–e003108. 20 indexed citations

Addissie, Yonit A., Paul Kruszka, Zoë C. Wong, et al.. (2020). Prenatal exposure to pesticides and risk for holoprosencephaly: a case-control study. Environmental Health. 19(1). 65–65. 27 indexed citations

Hadley, Donald W., et al.. (2020). Uptake and predictors of colonoscopy use in family members not participating in cascade genetic testing for Lynch syndrome. Scientific Reports. 10(1). 15959–15959. 4 indexed citations

Addissie, Yonit A., Zoë C. Wong, Joshua L. Everson, et al.. (2020). Identifying environmental risk factors and gene–environment interactions in holoprosencephaly. Birth Defects Research. 113(1). 63–76. 13 indexed citations

Kruszka, Paul, Ashley Buscetta, Maria T. Acosta, et al.. (2019). Circle of Willis anomalies in Turner syndrome: Absent A1 segment of the anterior cerebral artery. Birth Defects Research. 111(19). 1584–1588. 2 indexed citations

Ekure, Ekanem N., Yonit A. Addissie, Ogochukwu Sokunbi, et al.. (2019). Tuberous sclerosis in a patient from Nigeria. American Journal of Medical Genetics Part A. 179(8). 1423–1425. 3 indexed citations

Kruszka, Paul, Yonit A. Addissie, Donald W. Hadley, et al.. (2016). Muenke syndrome: An international multicenter natural history study. American Journal of Medical Genetics Part A. 170(4). 918–929. 31 indexed citations

Addissie, Yonit A., Donald W. Hadley, María J. Guillen Sacoto, et al.. (2015). Executive Function and Adaptive Behavior in Muenke Syndrome. The Journal of Pediatrics. 167(2). 428–434. 9 indexed citations

10.

Addissie, Yonit A., et al.. (2015). Muenke syndrome. 4(1). 1–6. 1 indexed citations

11.

Addissie, Yonit A., et al.. (2015). Craniosynostosis and Noonan syndrome withKRASmutations: Expanding the phenotype with a case report and review of the literature. American Journal of Medical Genetics Part A. 167(11). 2657–2663. 34 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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