Lauren Grote

431 total citations
7 papers, 186 citations indexed

About

Lauren Grote is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lauren Grote has authored 7 papers receiving a total of 186 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lauren Grote's work include Genomics and Rare Diseases (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Lauren Grote is often cited by papers focused on Genomics and Rare Diseases (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Lauren Grote collaborates with scholars based in United States and Italy. Lauren Grote's co-authors include Kristen L. Sund, Isabelle Thiffault, Lisa J. Martin, Carol Saunders, Sarah Zimmerman, Emily Farrow, Cameron Thomas, Teresa A. Smolarek, Anna L. Mitchell and Carlos E. Prada and has published in prestigious journals such as The Journal of General Physiology, Genetics in Medicine and American Journal of Medical Genetics Part A.

In The Last Decade

Lauren Grote

7 papers receiving 184 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lauren Grote United States	6	105	88	36	33	24	7	186
Filip Roelens Belgium	10	160 1.5×	141 1.6×	34 0.9×	46 1.4×	37 1.5×	17	346
Katja Kloth Germany	10	127 1.2×	112 1.3×	22 0.6×	22 0.7×	14 0.6×	18	238
Keri Ramsey United States	10	163 1.6×	97 1.1×	27 0.8×	18 0.5×	9 0.4×	14	255
Xue‐Xue Zhu United States	7	118 1.1×	108 1.2×	34 0.9×	27 0.8×	35 1.5×	11	393
Juliette Piard France	10	151 1.4×	121 1.4×	22 0.6×	16 0.5×	10 0.4×	24	253
Shinobu Fukumura Japan	11	149 1.4×	55 0.6×	44 1.2×	26 0.8×	11 0.5×	29	272
Helle Lybæk Norway	10	114 1.1×	162 1.8×	26 0.7×	44 1.3×	22 0.9×	15	282
Frédérique Sloan‐Béna Switzerland	9	123 1.2×	87 1.0×	16 0.4×	30 0.9×	7 0.3×	23	263
Fabíola Paoli Monteiro Brazil	11	198 1.9×	138 1.6×	28 0.8×	12 0.4×	18 0.8×	24	314
Chris Esapa United Kingdom	8	271 2.6×	92 1.0×	48 1.3×	14 0.4×	15 0.6×	9	320

Countries citing papers authored by Lauren Grote

Since Specialization

Citations

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

Fields of papers citing papers by Lauren Grote

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lauren Grote

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

All Works

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7 of 7 papers shown

Grote, Lauren, Isabelle Thiffault, Emily Farrow, et al.. (2018). Incidental diagnosis of tuberous sclerosis complex by exome sequencing in three families with subclinical findings. Neurogenetics. 19(3). 205–213. 6 indexed citations

Grote, Lauren, Elena Repnikova, & Shivarajan Amudhavalli. (2015). Expanding the phenotype of feingold syndrome‐2. American Journal of Medical Genetics Part A. 167(12). 3219–3225. 13 indexed citations

Thiffault, Isabelle, Carol Saunders, Nikita Raje, et al.. (2015). A patient with polymerase E1 deficiency (POLE1): clinical features and overlap with DNA breakage/instability syndromes. BMC Medical Genetics. 16(1). 31–31. 22 indexed citations

Thiffault, Isabelle, David J. Speca, Daniel C. Austin, et al.. (2015). A novel epileptic encephalopathy mutation in KCNB1 disrupts Kv2.1 ion selectivity, expression, and localization. The Journal of General Physiology. 146(5). 399–410. 66 indexed citations

Grote, Lauren, Melanie F. Myers, Anne M. Lovell, Howard M. Saal, & Kristen L. Sund. (2013). Variable approaches to genetic counseling for microarray regions of homozygosity associated with parental relatedness. American Journal of Medical Genetics Part A. 164(1). 87–98. 4 indexed citations

Sund, Kristen L., Sarah Zimmerman, Cameron Thomas, et al.. (2012). Regions of homozygosity identified by SNP microarray analysis aid in the diagnosis of autosomal recessive disease and incidentally detect parental blood relationships. Genetics in Medicine. 15(1). 70–78. 61 indexed citations

Grote, Lauren, Melanie F. Myers, Anne M. Lovell, Howard M. Saal, & Kristen L. Sund. (2012). Variability in laboratory reporting practices for regions of homozygosity indicating parental relatedness as identified by SNP microarray testing. Genetics in Medicine. 14(12). 971–976. 14 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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