Meredith Weaver

914 total citations
15 papers, 226 citations indexed

About

Meredith Weaver is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Meredith Weaver has authored 15 papers receiving a total of 226 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 4 papers in Clinical Biochemistry. Recurrent topics in Meredith Weaver's work include Genomics and Rare Diseases (5 papers), Metabolism and Genetic Disorders (4 papers) and Intellectual Property and Patents (3 papers). Meredith Weaver is often cited by papers focused on Genomics and Rare Diseases (5 papers), Metabolism and Genetic Disorders (4 papers) and Intellectual Property and Patents (3 papers). Meredith Weaver collaborates with scholars based in United States, Canada and Spain. Meredith Weaver's co-authors include Mildred K. Cho, Jon F. Merz, Debra G. B. Leonard, Samantha Illangasekare, Michael S. Watson, Sharon E. Plon, Toni I. Pollin, Reece K. Hart, Christine Micheel and Deborah Ritter and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and Genetics in Medicine.

In The Last Decade

Meredith Weaver

12 papers receiving 207 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Meredith Weaver United States	7	104	74	70	66	59	15	226
Carol Isaacson Barash United States	9	18 0.2×	55 0.7×	159 2.3×	48 0.7×	16 0.3×	14	328
Marlene E. Haffner United States	9	36 0.3×	55 0.7×	85 1.2×	49 0.7×	167 2.8×	23	323
James Valentine United States	4	5 0.0×	24 0.3×	96 1.4×	129 2.0×	74 1.3×	7	315
Josep Torrent-Farnell Spain	6	27 0.3×	29 0.4×	37 0.5×	28 0.4×	164 2.8×	10	256
Hanna I. Hyry United Kingdom	7	16 0.2×	11 0.1×	31 0.4×	34 0.5×	128 2.2×	8	230
Enrico Costa Italy	8	13 0.1×	17 0.2×	39 0.6×	39 0.6×	91 1.5×	26	284
David Glazer Canada	4	3 0.0×	127 1.7×	187 2.7×	91 1.4×	41 0.7×	7	343
Eline Picavet Belgium	11	40 0.4×	23 0.3×	44 0.6×	27 0.4×	217 3.7×	20	299
Francis Arickx Belgium	6	14 0.1×	10 0.1×	22 0.3×	15 0.2×	160 2.7×	11	209
Jong Hyuk Lee South Korea	9	11 0.1×	7 0.1×	32 0.5×	69 1.0×	83 1.4×	24	271

Countries citing papers authored by Meredith Weaver

Since Specialization

Citations

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

Fields of papers citing papers by Meredith Weaver

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Meredith Weaver

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

All Works

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15 of 15 papers shown

Mew, Nicholas Ah, Ljubica Caldovic, Annette Feigenbaum, et al.. (2024). P007: PP4 criteria specifications for proximal urea cycle disorders*. SHILAP Revista de lepidopterología. 2. 100884–100884.

Groopman, Emily, Shruthi Mohan, Raquel Fernández, et al.. (2024). Assessment of genes involved in lysosomal diseases using the ClinGen clinical validity framework. Molecular Genetics and Metabolism. 143(3). 108593–108593.

Goldstein, Jennifer, Amanda Thomas‐Wilson, Emily Groopman, et al.. (2024). ClinGen variant curation expert panel recommendations for classification of variants in GAMT, GATM and SLC6A8 for cerebral creatine deficiency syndromes. Molecular Genetics and Metabolism. 142(1). 108362–108362. 4 indexed citations

Dickson, Alexa, Marcus J. Miller, Elaine Spector, et al.. (2023). Specifications of the ACMG/AMP guidelines for ACADVL variant interpretation. Molecular Genetics and Metabolism. 140(3). 107668–107668. 1 indexed citations

Mohan, Shruthi, Meredith Weaver, Irene De Biase, et al.. (2023). Evaluating the strength of evidence for genes implicated in peroxisomal disorders using the ClinGen clinical validity framework and providing updates to the peroxisomal disease nomenclature. Molecular Genetics and Metabolism. 139(3). 107604–107604.

Caldovic, Ljubica, William Craigen, Annette Feigenbaum, et al.. (2023). CURATION OF SEQUENCE VARIANTS IN UREA CYCLE GENES. Molecular Genetics and Metabolism. 138(3). 107488–107488. 1 indexed citations

McGlaughon, Jennifer, Marzia Pasquali, Kathleen Wallace, et al.. (2019). Assessing the strength of evidence for genes implicated in fatty acid oxidation disorders using the ClinGen clinical validity framework. Molecular Genetics and Metabolism. 128(1-2). 122–128. 2 indexed citations

Milko, Laura V., Birgit Funke, Ray E. Hershberger, et al.. (2018). Development of Clinical Domain Working Groups for the Clinical Genome Resource (ClinGen): lessons learned and plans for the future. Genetics in Medicine. 21(4). 987–993. 13 indexed citations

Ritter, Deborah, Sameek Roychowdhury, Angshumoy Roy, et al.. (2016). Somatic cancer variant curation and harmonization through consensus minimum variant level data. Genome Medicine. 8(1). 117–117. 42 indexed citations

10.

Lewis, Katie L., et al.. (2016). The Dynamics of a Genetic Counseling Peer Supervision Group. Journal of Genetic Counseling. 26(3). 532–540. 8 indexed citations

11.

Weaver, Meredith & Toni I. Pollin. (2012). Direct‐to‐Consumer Genetic Testing: What Are We Talking About?. Journal of Genetic Counseling. 21(3). 361–366. 6 indexed citations

12.

Weaver, Meredith, et al.. (2010). Medical foods: Inborn errors of metabolism and the reimbursement dilemma. Genetics in Medicine. 12(6). 364–369. 11 indexed citations

13.

Cho, Mildred K., et al.. (2003). A Pilot Survey on the Licensing of DNA Inventions. The Journal of Law Medicine & Ethics. 31(3). 442–449. 10 indexed citations

14.

Cho, Mildred K., Samantha Illangasekare, Meredith Weaver, Debra G. B. Leonard, & Jon F. Merz. (2003). Effects of Patents and Licenses on the Provision of Clinical Genetic Testing Services. Journal of Molecular Diagnostics. 5(1). 3–8. 107 indexed citations

15.

Cho, Mildred K., et al.. (2002). DNA Patenting and Licensing. Science. 297(5585). 1279–1279. 21 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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