Alecia Willis

4.4k total citations
17 papers, 643 citations indexed

About

Alecia Willis is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Alecia Willis has authored 17 papers receiving a total of 643 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 5 papers in Genetics. Recurrent topics in Alecia Willis's work include Metabolism and Genetic Disorders (6 papers), Biochemical and Molecular Research (3 papers) and Folate and B Vitamins Research (3 papers). Alecia Willis is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Biochemical and Molecular Research (3 papers) and Folate and B Vitamins Research (3 papers). Alecia Willis collaborates with scholars based in United States, Spain and Ghana. Alecia Willis's co-authors include David Valle, Hans‐Ulrich Bender, Gary Steel, Marshall Summar, Ann E. Pulver, Wei‐Wen Lin, Shlomo Almashanu, Chien-an A. Hu, Lee‐Jun C. Wong and Christine M. Eng and has published in prestigious journals such as Free Radical Biology and Medicine, The American Journal of Human Genetics and Gene.

In The Last Decade

Alecia Willis

16 papers receiving 632 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Alecia Willis United States	14	373	195	132	77	69	17	643
Tamara Ramadan Switzerland	10	361 1.0×	60 0.3×	132 1.0×	101 1.3×	285 4.1×	11	832
Mohammed Almannai Saudi Arabia	17	597 1.6×	137 0.7×	381 2.9×	125 1.6×	40 0.6×	43	935
Lisa Emrick United States	15	486 1.3×	105 0.5×	290 2.2×	134 1.7×	47 0.7×	43	736
Chike Bellarmine Item Austria	17	348 0.9×	108 0.6×	360 2.7×	179 2.3×	59 0.9×	38	879
Helen Freeman United Kingdom	5	400 1.1×	177 0.9×	45 0.3×	232 3.0×	24 0.3×	5	744
Nicole Lesko Sweden	11	511 1.4×	79 0.4×	154 1.2×	43 0.6×	50 0.7×	23	652
Mehmet Seven Türkiye	15	304 0.8×	115 0.6×	67 0.5×	62 0.8×	22 0.3×	59	765
S. Lane Rutledge United States	19	844 2.3×	252 1.3×	519 3.9×	104 1.4×	66 1.0×	31	1.3k
J. M. van der Klei‐van Moorsel Netherlands	9	586 1.6×	101 0.5×	254 1.9×	110 1.4×	59 0.9×	10	786
Caroline A. Wallace United Kingdom	5	376 1.0×	171 0.9×	25 0.2×	184 2.4×	55 0.8×	6	652

Countries citing papers authored by Alecia Willis

Since Specialization

Citations

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

Fields of papers citing papers by Alecia Willis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alecia Willis

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

All Works

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17 of 17 papers shown

Song, Wei, Hayk Hovhannisyan, Wenjie Chen, et al.. (2015). Exploring the landscape of pathogenic genetic variation in the ExAC population database: insights of relevance to variant classification. Genetics in Medicine. 18(8). 850–854. 58 indexed citations

Posey, Jennifer E., Lindsay C. Burrage, Marcus J. Miller, et al.. (2014). Lysinuric protein intolerance presenting with multiple fractures. Molecular Genetics and Metabolism Reports. 1. 176–183. 18 indexed citations

Vatta, Matteo, Zhiyv Niu, James R. Lupski, et al.. (2013). Evidence for replicative mechanism in a CHD7 rearrangement in a patient with CHARGE syndrome. PMC.

Vatta, Matteo, Zhiyv Niu, James R. Lupski, et al.. (2013). Evidence for replicative mechanism in a CHD7 rearrangement in a patient with CHARGE syndrome. American Journal of Medical Genetics Part A. 161(12). 3182–3186. 5 indexed citations

Celestino-Soper, Patrícia B. S., Cindy Skinner, Richard J. Schroer, et al.. (2012). Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders. Molecular Cytogenetics. 5(1). 17–17. 41 indexed citations

Bekheirnia, Mir Reza, Victor Wei Zhang, Tanya N. Eble, et al.. (2012). POLG mutation in a patient with cataracts, early-onset distal muscle weakness and atrophy, ovarian dysgenesis and 3-methylglutaconic aciduria. Gene. 499(1). 209–212. 16 indexed citations

Willis, Alecia, Ignatia Van den Veyver, & Christine M. Eng. (2012). Multiplex ligation‐dependent probe amplification (MLPA) and prenatal diagnosis. Prenatal Diagnosis. 32(4). 315–320. 20 indexed citations

Yang, Yaping, et al.. (2011). Early onset obesity and adrenal insufficiency associated with a homozygous POMC mutation. International Journal of Pediatric Endocrinology. 2011(1). 5–5. 35 indexed citations

Häberle, Johannes, Oleg A. Shchelochkov, Jing Wang, et al.. (2010). Molecular defects in human carbamoy phosphate synthetase I: mutational spectrum, diagnostic and protein structure considerations. Human Mutation. 32(6). 579–589. 53 indexed citations

10.

Le, Truc M., Alecia Willis, Frances Barr, et al.. (2010). An ethnic-specific polymorphism in the catalytic subunit of glutamate-cysteine ligase impairs the production of glutathione intermediates in vitro. Molecular Genetics and Metabolism. 101(1). 55–61. 9 indexed citations

11.

Willis, Alecia, Hans‐Ulrich Bender, Gary Steel, & David Valle. (2008). PRODH variants and risk for schizophrenia. Amino Acids. 35(4). 673–679. 51 indexed citations

12.

Yadav, Meeta, et al.. (2006). The frequent observation of evidence for nonsense-mediated decay in RNA from patients with carbamyl phosphate synthetase I deficiency. Molecular Genetics and Metabolism. 89(1-2). 80–86. 14 indexed citations

13.

Bender, Hans‐Ulrich, Shlomo Almashanu, Gary Steel, et al.. (2005). Functional Consequences of PRODH Missense Mutations. The American Journal of Human Genetics. 76(3). 409–420. 110 indexed citations

14.

Williams, Scott M., Marylyn D. Ritchie, John A. Phillips, et al.. (2004). Multilocus Analysis of Hypertension: A Hierarchical Approach. Human Heredity. 57(1). 28–38. 112 indexed citations

15.

Summar, Marshall, Lynn Hall, Brian W. Christman, et al.. (2004). Environmentally determined genetic expression: clinical correlates with molecular variants of carbamyl phosphate synthetase I. Molecular Genetics and Metabolism. 81. 12–19. 38 indexed citations

16.

Summar, Marshall, Lynn Hall, Holli B. Hutcheson, et al.. (2003). Characterization of genomic structure and polymorphisms in the human carbamyl phosphate synthetase I gene. Gene. 311. 51–57. 46 indexed citations

17.

Willis, Alecia, Michael L. Freeman, Frances Barr, et al.. (2002). Ethnic diversity in a critical gene responsible for glutathione synthesis. Free Radical Biology and Medicine. 34(1). 72–76. 17 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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