Katrina Celis

463 total citations
9 papers, 81 citations indexed

About

Katrina Celis is a scholar working on Genetics, Molecular Biology and Physiology. According to data from OpenAlex, Katrina Celis has authored 9 papers receiving a total of 81 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Physiology. Recurrent topics in Katrina Celis's work include Genetic Associations and Epidemiology (2 papers), Alzheimer's disease research and treatments (2 papers) and Cleft Lip and Palate Research (2 papers). Katrina Celis is often cited by papers focused on Genetic Associations and Epidemiology (2 papers), Alzheimer's disease research and treatments (2 papers) and Cleft Lip and Palate Research (2 papers). Katrina Celis collaborates with scholars based in United States, Puerto Rico and Colombia. Katrina Celis's co-authors include Wendy K. Chung, Eden Haverfield, Edwin R. Guzman, Rongze Yang, Joshua Cappell, Sidney B. Eisig, Patricia Lanzano, Joseph Haddad, Da‐Wei Gong and Gloria H. Su and has published in prestigious journals such as Neurology, Journal of the Neurological Sciences and The Laryngoscope.

In The Last Decade

Katrina Celis

9 papers receiving 81 citations

Peers

Countries citing papers authored by Katrina Celis

Since Specialization

Citations

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

Fields of papers citing papers by Katrina Celis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Katrina Celis

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

All Works

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9 of 9 papers shown

#	Work	Indexed citations
1	Neuropsychiatric features in a multi‐ethnic population with Alzheimer disease and mild cognitive impairment 2023 ·International Journal of Geriatric Psychiatry ·Katrina Celis, (unknown), Larry D. Adams, (unknown), (unknown), Takiyah D. Starks, (unknown), Kara L. Hamilton‐Nelson, Pedro Mena, (unknown), Reneé A. Laux, Yeunjoo E. Song, Allison Caban‐Holt, (unknown), Jeffery M. Vance, Jonathan L. Haines, Goldie S. Byrd, Gary W. Beecham, Margaret A. Pericak‐Vance, Michael L. Cuccaro	2
2	Ancestry‐related differences in chromatin accessibility and gene expression of APOE ε4 are associated with Alzheimer's disease risk 2023 ·Alzheimer s & Dementia ·Katrina Celis, (unknown), Farid Rajabli, Patrice L. Whitehead, Kara L. Hamilton‐Nelson, Derek M. Dykxhoorn, Karen Nuytemans, Liyong Wang, Margaret E. Flanagan, Sandra Weıntraub, Changiz Geula, Marla Gearing, Clifton L. Dalgard, Fulai Jin, David A. Bennett, Theresa Schuck, Margaret A. Pericak‐Vance, Anthony J. Griswold, Juan I. Young, Jeffery M. Vance	4
3	Novel Variants in LRRK2 and GBA Identified in Latino Parkinson Disease Cohort Enriched for Caribbean Origin 2020 ·Frontiers in Neurology ·Karen Nuytemans, Farid Rajabli, Parker L. Bussies, Katrina Celis, William K. Scott, Carlos Singer, Corneliu Luca, Ángel Viñuela, Margaret A. Pericak‐Vance, Jeffery M. Vance	6
4	The Alzheimer’s disease sequencing project–follow up study (ADSP‐FUS): Increasing ethnic diversity in Alzheimer’s genetics research with addition of potential new cohorts 2020 ·Alzheimer s & Dementia ·Pedro Mena, Brian W. Kunkle, Kelley Faber, Katrina Celis, Larry D. Adams, Tatiana Foroud, Dolly Reyes‐Dumeyer, Amanda B Kuzma, Adam C. Naj, Eden R. Martin, Clifton L. Dalgard, Gerard D. Schellenberg, Weixin Wang, Jeffery M. Vance, Michael L. Cuccaro, Richard Mayeux, Badri N. Vardarajan, Margaret A. Pericak‐Vance	6
5	Transcriptome Analysis of Single Nucleus RNA-seq from Alzheimer Disease APOE4 Carrier Brains in African American (AA) and Non-Hispanic Whites (NHW) Reveals Differences in APOE Expression (4626) 2020 ·Neurology ·Katrina Celis, Anthony J. Griswold, Parker L. Bussies, Farid Rajabli, Patrice L. Whitehead, (unknown), Kara L. Hamilton‐Nelson, Eileen H. Bigio, Marsel Mesulam, Changiz Geula, Sandra Weıntraub, Marla Gearing, Gary W. Beecham, William K. Scott, Margaret A. Pericak‐Vance, Juan I. Young, Jeffery M. Vance	3
6	ACSS2 gene variant associated with cleft lip and palate in two independent Hispanic populations 2017 ·The Laryngoscope ·Sonam Dodhia, Katrina Celis, (unknown), Yi Cai, (unknown), (unknown), David Hoffman, (unknown), Sidney B. Eisig, Gloria H. Su, Wendy K. Chung, Joseph Haddad	2
7	African haplotypic background mitigates the effect of apoe ε4 risk allele in alzheimer disease 2017 ·Journal of the Neurological Sciences ·Margaret A. Pericak‐Vance, Farid Rajabli, (unknown), Katrina Celis, Kara L. Hamilton‐Nelson, (unknown), (unknown), Goldie S. Byrd, Jeffery M. Vance, (unknown), Jonathan L. Haines, Gary W. Beecham	2
8	Loss of function mutation in glutamic pyruvate transaminase 2 (GPT2) causes developmental encephalopathy 2015 ·Journal of Inherited Metabolic Disease ·Katrina Celis, (unknown), Eden Haverfield, Joshua Cappell, Rongze Yang, Da‐Wei Gong, Wendy K. Chung	20
9	Association of candidate genes with nonsyndromic clefts in Honduran and Colombian populations 2012 ·The Laryngoscope ·(unknown), Andrew C. Birkeland, (unknown), Gloria H. Su, Patricia Lanzano, Edwin R. Guzman, Katrina Celis, Sidney B. Eisig, David Hoffman, (unknown), (unknown), Wendy K. Chung, Joseph Haddad	36

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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