Luis Rohena

1.3k total citations
27 papers, 383 citations indexed

About

Luis Rohena is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Luis Rohena has authored 27 papers receiving a total of 383 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 12 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Luis Rohena's work include Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Congenital heart defects research (4 papers). Luis Rohena is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genetics and Neurodevelopmental Disorders (6 papers) and Congenital heart defects research (4 papers). Luis Rohena collaborates with scholars based in United States, Netherlands and China. Luis Rohena's co-authors include Wendy K. Chung, David T. Hsieh, Kelly Gonzalez, Orrin Devinsky, Sha Tang, Julie Neidich, Kwame Anyane‐Yeboa, Allison K. Cabalka, S Bentley and Timothy M. Olson and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and PLoS Genetics.

In The Last Decade

Luis Rohena

26 papers receiving 370 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Luis Rohena United States 12 192 154 52 47 46 27 383
Tawfeg Ben‐Omran Qatar 11 353 1.8× 225 1.5× 41 0.8× 43 0.9× 40 0.9× 24 584
Ardinger Hh United States 6 192 1.0× 124 0.8× 27 0.5× 37 0.8× 23 0.5× 287 402
Kit San Yeung Hong Kong 13 252 1.3× 245 1.6× 25 0.5× 40 0.9× 65 1.4× 29 529
Adam Mp 6 180 0.9× 113 0.7× 25 0.5× 37 0.8× 21 0.5× 286 388
Bean Ljh 6 180 0.9× 113 0.7× 25 0.5× 37 0.8× 21 0.5× 285 386
A Amemiya Japan 6 173 0.9× 104 0.7× 24 0.5× 37 0.8× 21 0.5× 269 377
Xingjian Jin United States 10 194 1.0× 217 1.4× 42 0.8× 29 0.6× 34 0.7× 11 312
Ender Karaca Türkiye 13 265 1.4× 247 1.6× 40 0.8× 33 0.7× 40 0.9× 25 544
Teresa Neuhann Germany 14 215 1.1× 189 1.2× 28 0.5× 43 0.9× 62 1.3× 38 425
Bird Td United States 6 162 0.8× 90 0.6× 22 0.4× 35 0.7× 20 0.4× 244 342

Countries citing papers authored by Luis Rohena

Since Specialization
Citations

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

Fields of papers citing papers by Luis Rohena

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luis Rohena

This figure shows the co-authorship network connecting the top 25 collaborators of Luis Rohena. A scholar is included among the top collaborators of Luis Rohena 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 Luis Rohena. Luis Rohena 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.
Ward, Scott, Paul J. Benke, Lisa Emrick, et al.. (2023). De novo missense variants in ZBTB47 are associated with developmental delays, hypotonia, seizures, gait abnormalities, and variable movement abnormalities. American Journal of Medical Genetics Part A. 194(1). 17–30.
2.
Hsieh, David T., et al.. (2020). Lisch nodules and iris mammillations in two siblings with familial legius syndrome. SHILAP Revista de lepidopterología. 8(10). 1867–1871. 2 indexed citations
3.
Rohena, Luis, et al.. (2020). A case series of a mother and two daughters with a GLI2 gene deletion demonstrating variable expressivity and incomplete penetrance. SHILAP Revista de lepidopterología. 8(11). 2138–2144. 9 indexed citations
4.
Starokadomskyy, Petro, Katelynn M. Wilton, Konrad Krzewski, et al.. (2019). NK cell defects in X-linked pigmentary reticulate disorder. JCI Insight. 4(21). 15 indexed citations
5.
Esch, Hilde Van, Rita Colnaghi, Kathleen Freson, et al.. (2019). Defective DNA Polymerase α-Primase Leads to X-Linked Intellectual Disability Associated with Severe Growth Retardation, Microcephaly, and Hypogonadism. The American Journal of Human Genetics. 104(5). 957–967. 26 indexed citations
6.
Faux, Brian M., et al.. (2018). Youngest presenting patient with dystonia 24 and review of the literature. Clinical Case Reports. 6(11). 2070–2074. 12 indexed citations
7.
Rohena, Luis, et al.. (2018). Fashionably Late: A Case of Delayed Cutaneous Manifestations in Juvenile Dermatomyositis. Journal of Clinical Medicine Research. 10(11). 848–852. 3 indexed citations
8.
Smith, Stephen A., et al.. (2017). Novel case of paternal paracentric inversion causing partial trisomy 13 and review of the literature. American Journal of Medical Genetics Part A. 173(6). 1673–1680. 2 indexed citations
9.
Hsieh, David T., et al.. (2017). Somatic Mosaicism of PCDH19 in a male with early infantile epileptic encephalopathy and review of the literature. American Journal of Medical Genetics Part A. 173(6). 1625–1630. 19 indexed citations
10.
Rohena, Luis, et al.. (2017). Rare presentation of 6q16.3 microdeletion syndrome with severe upper limb reduction defects and duodenal atresia. Clinical Case Reports. 5(6). 905–914. 1 indexed citations
11.
Hogue, Jacob S., et al.. (2017). Tetraploid–diploid mosaicism in a patient with pigmentary anomalies of hair and skin: a new dermatologic feature. Clinical Case Reports. 6(1). 103–108. 4 indexed citations
12.
Kelle, Angela M., S Bentley, Luis Rohena, Allison K. Cabalka, & Timothy M. Olson. (2016). Ebstein anomaly, left ventricular non‐compaction, and early onset heart failure associated with a de novo α‐tropomyosin gene mutation. American Journal of Medical Genetics Part A. 170(8). 2186–2190. 25 indexed citations
13.
Rohena, Luis, et al.. (2016). Encephalocraniocutaneous lipomatosis (Haberland syndrome): A mild case with bilateral cutaneous and ocular involvement. JAAD Case Reports. 2(2). 150–152. 9 indexed citations
14.
Tang, Sha, Russell S. Miller, Luis Rohena, et al.. (2015). New Insights into the Genetics of Fetal Megacystis: ACTG2 Mutations, Encoding γ-2 Smooth Muscle Actin in Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (Berdon Syndrome). Fetal Diagnosis and Therapy. 38(4). 296–306. 40 indexed citations
15.
Rohena, Luis, Edwin R. Guzman, Mythily Ganapathi, et al.. (2015). FTO variant associated with malformation syndrome. American Journal of Medical Genetics Part A. 170(4). 1023–1028. 14 indexed citations
16.
Hsieh, David T., et al.. (2015). Infantile onset Vanishing White Matter disease associated with a novel EIF2B5 variant, remarkably long life span, severe epilepsy, and hypopituitarism. American Journal of Medical Genetics Part A. 167(4). 826–830. 5 indexed citations
17.
Shang, Linshan, Megan T. Cho, Kyle Retterer, et al.. (2015). Mutations in ARID2 are associated with intellectual disabilities. Neurogenetics. 16(4). 307–314. 43 indexed citations
18.
DeStefano, Gina M., Mazen Kurban, Kwame Anyane‐Yeboa, et al.. (2014). Mutations in the Cholesterol Transporter Gene ABCA5 Are Associated with Excessive Hair Overgrowth. PLoS Genetics. 10(5). e1004333–e1004333. 39 indexed citations
19.
Rohena, Luis, Julie Neidich, Kelly Gonzalez, et al.. (2013). Mutation inSNAP25as a novel genetic cause of epilepsy and intellectual disability. PubMed. 1(1). e26314–e26314. 53 indexed citations
20.
Rohena, Luis, et al.. (2011). Evidence for autosomal dominant inheritance of ablepharon-macrostomia syndrome. American Journal of Medical Genetics Part A. 155(4). 850–854. 8 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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