Danielle LaGrave

524 total citations
11 papers, 327 citations indexed

About

Danielle LaGrave is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Infectious Diseases. According to data from OpenAlex, Danielle LaGrave has authored 11 papers receiving a total of 327 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 6 papers in Genetics and 2 papers in Infectious Diseases. Recurrent topics in Danielle LaGrave's work include Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Danielle LaGrave is often cited by papers focused on Prenatal Screening and Diagnostics (6 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (2 papers). Danielle LaGrave collaborates with scholars based in United States. Danielle LaGrave's co-authors include Patti Krautscheid, Erin E. Baldwin, Christine E. Miller, Kim Hart, Tatiana Tvrdik, Nancy C. Rose, Kathryn L. Berrier, Cori Feist, Diane Masser‐Frye and Blythe G. Crissman and has published in prestigious journals such as American Journal of Clinical Pathology, Genetics in Medicine and Journal of Child Neurology.

In The Last Decade

Danielle LaGrave

11 papers receiving 315 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Danielle LaGrave United States 8 200 129 56 51 43 11 327
Campbell K. Brasington United States 6 310 1.6× 119 0.9× 61 1.1× 60 1.2× 66 1.5× 8 421
L. Butler United Kingdom 6 227 1.1× 123 1.0× 27 0.5× 34 0.7× 73 1.7× 8 378
Cori Feist United States 6 123 0.6× 54 0.4× 38 0.7× 29 0.6× 17 0.4× 13 209
Antina de Jong Netherlands 9 378 1.9× 139 1.1× 91 1.6× 32 0.6× 56 1.3× 9 453
Zuzana Deans United Kingdom 9 299 1.5× 47 0.4× 87 1.6× 22 0.4× 62 1.4× 16 353
Mitsuyo Tanemura Japan 12 148 0.7× 85 0.7× 34 0.6× 43 0.8× 39 0.9× 27 359
Hook Eb United States 5 293 1.5× 108 0.8× 100 1.8× 55 1.1× 26 0.6× 8 446
Amy Swanson United States 9 194 1.0× 99 0.8× 20 0.4× 29 0.6× 71 1.7× 18 293
Elisabeth Siti Herini Indonesia 9 63 0.3× 30 0.2× 26 0.5× 35 0.7× 28 0.7× 56 236
Rebecca Rae Anderson United States 3 125 0.6× 215 1.7× 71 1.3× 53 1.0× 5 0.1× 7 362

Countries citing papers authored by Danielle LaGrave

Since Specialization
Citations

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

Fields of papers citing papers by Danielle LaGrave

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Danielle LaGrave

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

All Works

11 of 11 papers shown
1.
Rose, Nancy C., Elizabeth S. Barrie, Jennifer Malinowski, et al.. (2022). Systematic evidence-based review: The application of noninvasive prenatal screening using cell-free DNA in general-risk pregnancies. Genetics in Medicine. 24(7). 1379–1391. 46 indexed citations
2.
La’ulu, Sonia L., et al.. (2021). Tobacco and Cannabis Use During Pregnancy. American Journal of Clinical Pathology. 157(1). 146–152. 1 indexed citations
3.
Martin, Kimberly, Carole Samango‐Sprouse, Danielle LaGrave, et al.. (2020). Detection of maternal X chromosome abnormalities using single nucleotide polymorphism–based noninvasive prenatal testing. American Journal of Obstetrics & Gynecology MFM. 2(3). 100152–100152. 10 indexed citations
4.
Herriges, John, et al.. (2018). Delineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature. Journal of Child Neurology. 34(2). 86–93. 1 indexed citations
5.
LaGrave, Danielle, et al.. (2016). Xq11.1-11.2 deletion involving ARHGEF9 in a girl with autism spectrum disorder. European Journal of Medical Genetics. 59(9). 470–473. 19 indexed citations
6.
Miller, Christine E., Patti Krautscheid, Erin E. Baldwin, et al.. (2014). Genetic counselor review of genetic test orders in a reference laboratory reduces unnecessary testing. American Journal of Medical Genetics Part A. 164(5). 1094–1101. 98 indexed citations
7.
Walker, Brandon S., Brian R. Jackson, Danielle LaGrave, Edward R. Ashwood, & Robert L. Schmidt. (2014). A cost‐effectiveness analysis of cell free DNA as a replacement for serum screening for Down syndrome. Prenatal Diagnosis. 35(5). 440–446. 34 indexed citations
8.
Rose, Nancy C., et al.. (2013). The impact of utilization of early aneuploidy screening on amniocenteses available for training in obstetrics and fetal medicine. Prenatal Diagnosis. 33(3). 242–244. 12 indexed citations
9.
Walker, Brandon S., Edward R. Ashwood, Brian R. Jackson, & Danielle LaGrave. (2013). A tradeoff analysis of risk cutoffs for the quadruple serum screen for Down syndrome. Prenatal Diagnosis. 33(12). 1201–1206. 2 indexed citations
10.
Millson, Alison, Danielle LaGrave, Mary Willis, et al.. (2011). Chromosomal loss of 3q26.3‐3q26.32, involving a partial neuroligin 1 deletion, identified by genomic microarray in a child with microcephaly, seizure disorder, and severe intellectual disability. American Journal of Medical Genetics Part A. 158A(1). 159–165. 20 indexed citations
11.
Berrier, Kathryn L., Blythe G. Crissman, Cori Feist, et al.. (2011). Practice Guidelines for Communicating a Prenatal or Postnatal Diagnosis of Down Syndrome: Recommendations of the National Society of Genetic Counselors. Journal of Genetic Counseling. 20(5). 432–441. 84 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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