Monique Williams

3.6k total citations
56 papers, 1.4k citations indexed

About

Monique Williams is a scholar working on Clinical Biochemistry, Molecular Biology and Psychiatry and Mental health. According to data from OpenAlex, Monique Williams has authored 56 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Clinical Biochemistry, 18 papers in Molecular Biology and 15 papers in Psychiatry and Mental health. Recurrent topics in Monique Williams's work include Metabolism and Genetic Disorders (23 papers), Dementia and Cognitive Impairment Research (11 papers) and Folate and B Vitamins Research (8 papers). Monique Williams is often cited by papers focused on Metabolism and Genetic Disorders (23 papers), Dementia and Cognitive Impairment Research (11 papers) and Folate and B Vitamins Research (8 papers). Monique Williams collaborates with scholars based in Netherlands, United States and France. Monique Williams's co-authors include John C. Morris, Catherine M. Roe, Chengjie Xiong, James E. Galvin, Hildegard M. Schuller, Howard K. Plummer, Patricia K. Tithof, Martha Storandt, Ganesh M. Babulal and Femke Molema and has published in prestigious journals such as PLoS ONE, Neurology and Diabetes Care.

In The Last Decade

Monique Williams

54 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Monique Williams Netherlands	22	425	410	409	320	165	56	1.4k
Cristina Sierra Spain	30	234 0.6×	353 0.9×	561 1.4×	295 0.9×	229 1.4×	140	2.6k
Dries Dobbelaere France	18	87 0.2×	478 1.2×	461 1.1×	243 0.8×	169 1.0×	42	1.3k
Gerard D. Schellenberg United States	18	438 1.0×	286 0.7×	486 1.2×	841 2.6×	53 0.3×	30	1.7k
Sumit Parikh United States	22	223 0.5×	811 2.0×	1.5k 3.6×	207 0.6×	70 0.4×	70	2.4k
Nobuto Shibata Japan	21	251 0.6×	90 0.2×	529 1.3×	564 1.8×	83 0.5×	101	1.6k
Björn Regland Sweden	29	575 1.4×	154 0.4×	453 1.1×	652 2.0×	972 5.9×	50	2.3k
Kim A. Jobst United Kingdom	15	522 1.2×	139 0.3×	303 0.7×	602 1.9×	889 5.4×	23	2.5k
Jean‐Marie Sérot France	17	112 0.3×	107 0.3×	302 0.7×	455 1.4×	76 0.5×	26	1.3k
Holly R. Thomasson United States	22	192 0.5×	55 0.1×	446 1.1×	177 0.6×	94 0.6×	29	2.2k

Countries citing papers authored by Monique Williams

Since Specialization

Citations

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

Fields of papers citing papers by Monique Williams

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monique Williams

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

All Works

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20 of 20 papers shown

Trani, Jean‐Francois, Samantha Murphy, Monique Williams, et al.. (2024). Recruiting a prospective community cohort to study Alzheimer's disease and structural and social determinants of health among adults racialized as Black: The ARCHES cohort. Alzheimer s & Dementia Translational Research & Clinical Interventions. 10(2). e12473–e12473. 4 indexed citations

Weinstein, David A., R. Jackson, Monique Williams, et al.. (2024). Short and long-term acceptability and efficacy of extended-release cornstarch in the hepatic glycogen storage diseases: results from the Glyde study. Orphanet Journal of Rare Diseases. 19(1). 258–258. 2 indexed citations

Sikkema‐Raddatz, Birgit, Terry G. J. Derks, Clara D.M. van Karnebeek, et al.. (2024). Newborn Screening by DNA-First: Systematic Evaluation of the Eligibility of Inherited Metabolic Disorders Based on Treatability. International Journal of Neonatal Screening. 11(1). 1–1. 2 indexed citations

Strijker, Marin, Laura A. Tseng, Curtis R. Coughlin, et al.. (2021). Cognitive and neurological outcome of patients in the Dutch pyridoxine-dependent epilepsy (PDE-ALDH7A1) cohort, a cross-sectional study. European Journal of Paediatric Neurology. 33. 112–120. 10 indexed citations

Mathison, Angela, Thiago M. de Assuncao, Monique Williams, et al.. (2020). Discovery, expression, cellular localization, and molecular properties of a novel, alternative spliced HP1γ isoform, lacking the chromoshadow domain. PLoS ONE. 15(2). e0217452–e0217452. 6 indexed citations

Peetsold, Marieke G., et al.. (2020). Fumarase Deficiency: A Case With a New Pathogenic Mutation and a Review of the Literature. Journal of Child Neurology. 36(4). 310–323. 6 indexed citations

Stout, Sarah H., Ganesh M. Babulal, Margaret Johnson, Monique Williams, & Catherine M. Roe. (2020). Recruitment of African American and Non-Hispanic White Older Adults for Alzheimer Disease Research Via Traditional and Social Media: a Case Study. Journal of Cross-Cultural Gerontology. 35(3). 329–339. 13 indexed citations

Bosch, Annet M., Margot F. Mulder, M. Estela Rubio‐Gozalbo, et al.. (2019). A nationwide retrospective observational study of population newborn screening for medium‐chain acyl‐CoA dehydrogenase (MCAD) deficiency in the Netherlands. Journal of Inherited Metabolic Disease. 42(5). 890–897. 22 indexed citations

Bleeker, Jeannette C., Sacha Ferdinandusse, Maaike de Vries, et al.. (2019). Proposal for an individualized dietary strategy in patients with very long‐chain acyl‐CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 42(1). 159–168. 18 indexed citations

10.

Molema, Femke, Florian Gleich, Peter Burgard, et al.. (2019). Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea‐cycle disorders: On the basis of information from a European multicenter registry. Journal of Inherited Metabolic Disease. 42(6). 1162–1175. 26 indexed citations

11.

Williams, Monique, Alberto Burlina, Laura Rubert, et al.. (2018). N-Acetylglutamate Synthase Deficiency Due to a Recurrent Sequence Variant in the N-acetylglutamate Synthase Enhancer Region. Scientific Reports. 8(1). 15436–15436. 8 indexed citations

12.

Mathison, Angela, Monique Williams, Asha Nair, et al.. (2017). Combined AURKA and H3K9 Methyltransferase Targeting Inhibits Cell Growth By Inducing Mitotic Catastrophe. Molecular Cancer Research. 15(8). 984–997. 12 indexed citations

13.

Mulder, Monique T., et al.. (2017). Low-density lipoprotein receptor–negative compound heterozygous familial hypercholesterolemia: Two lifetime journeys of lipid-lowering therapy. Journal of clinical lipidology. 11(1). 301–305. 3 indexed citations

14.

Kruijshaar, Michelle E., Rick van Minkelen, W. Onkenhout, et al.. (2016). Neonatal screening for profound biotinidase deficiency in the Netherlands: consequences and considerations. European Journal of Human Genetics. 24(10). 1424–1429. 18 indexed citations

15.

Welling, Lindsey, Anita Boelen, Terry G. J. Derks, et al.. (2016). Nine years of newborn screening for classical galactosemia in the Netherlands: Effectiveness of screening methods, and identification of patients with previously unreported phenotypes. Molecular Genetics and Metabolism. 120(3). 223–228. 34 indexed citations

16.

Visser, Gepke, et al.. (2016). Occurrence of subdural hematomas in Dutch glutaric aciduria type 1 patients. European Journal of Pediatrics. 175(7). 1001–1006. 15 indexed citations

17.

Louw, Elles van der, T.J. Williams, Bobbie J. Henry-Barron, et al.. (2016). Ketogenic diet therapy for epilepsy during pregnancy: A case series. Seizure. 45. 198–201. 31 indexed citations

18.

Versmissen, Jorie, et al.. (2015). Cascade screening of familial hypercholesterolemia must go on. Atherosclerosis. 242(2). 415–417. 22 indexed citations

19.

Roe, Catherine M., Anne M. Fagan, Monique Williams, et al.. (2011). Improving CSF biomarker accuracy in predicting prevalent and incident Alzheimer disease. Neurology. 76(6). 501–510. 35 indexed citations

20.

Schuller, Hildegard M., Patricia K. Tithof, Monique Williams, & Howard K. Plummer. (1999). The tobacco-specific carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone is a beta-adrenergic agonist and stimulates DNA synthesis in lung adenocarcinoma via beta-adrenergic receptor-mediated release of arachidonic acid.. PubMed. 59(18). 4510–5. 162 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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