Lauren Westerfield

485 total citations
11 papers, 183 citations indexed

About

Lauren Westerfield is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Lauren Westerfield has authored 11 papers receiving a total of 183 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Pediatrics, Perinatology and Child Health, 4 papers in Genetics and 3 papers in Molecular Biology. Recurrent topics in Lauren Westerfield's work include Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Lauren Westerfield is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Lauren Westerfield collaborates with scholars based in United States, Russia and Australia. Lauren Westerfield's co-authors include Ignatia Van den Veyver, Sandra Darilek, Ignatia B. Van den Veyver, Lisa M. Oakes, Christine M. Eng, Jennifer Malinowski, Yaping Yang, Tomi L. Toler, Karin J. Blakemore and Blair Stevens and has published in prestigious journals such as The American Journal of Human Genetics, Fertility and Sterility and Ultrasound in Obstetrics and Gynecology.

In The Last Decade

Lauren Westerfield

10 papers receiving 180 citations

Peers

Lauren Westerfield
Matthew A. Deardorff United States
Paulette Barahona Australia
Aurélie Coussement France
Nada Alsahan Saudi Arabia
M.T. Jones United Kingdom
Jennifer Saucier United States
Ebony Richardson Australia
Sara Caylor United States
Tristan Hardy Australia
Erica Schindewolf United States
Matthew A. Deardorff United States
Lauren Westerfield
Citations per year, relative to Lauren Westerfield Lauren Westerfield (= 1×) peers Matthew A. Deardorff

Countries citing papers authored by Lauren Westerfield

Since Specialization
Citations

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

Fields of papers citing papers by Lauren Westerfield

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lauren Westerfield

This figure shows the co-authorship network connecting the top 25 collaborators of Lauren Westerfield. A scholar is included among the top collaborators of Lauren Westerfield 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 Westerfield. Lauren Westerfield 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.
2.
Westerfield, Lauren, E. Andres Rivera-Munoz, Haowei Du, et al.. (2025). Improving automated deep phenotyping through large language models using retrieval-augmented generation. Genome Medicine. 17(1). 91–91. 1 indexed citations
3.
Zemet, Roni, Eyal Krispin, Lauren Westerfield, et al.. (2023). Implication of chromosomal microarray analysis prior to in‐utero repair of fetal open neural tube defect. Ultrasound in Obstetrics and Gynecology. 61(6). 719–727. 3 indexed citations
4.
Malinowski, Jennifer, Lauren Westerfield, Tomi L. Toler, et al.. (2023). Expanded carrier screening for reproductive risk assessment: An evidence‐based practice guideline from the National Society of Genetic Counselors. Journal of Genetic Counseling. 32(3). 540–557. 33 indexed citations
5.
Wynn, Julia, Jessica L. Giordano, Lauren Westerfield, et al.. (2022). Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies. Prenatal Diagnosis. 42(7). 947–954. 7 indexed citations
6.
Rosenfeld, Jill A., Lauren Westerfield, Amanda Gerard, et al.. (2021). Clinical characterization of individuals with the distal 1q21.1 microdeletion. American Journal of Medical Genetics Part A. 185(5). 1388–1398. 13 indexed citations
7.
Arian, Sara E., et al.. (2020). Prenatal testing in pregnancies conceived by in vitro fertilization with pre‐implantation genetic testing. Prenatal Diagnosis. 40(7). 846–851. 2 indexed citations
8.
Szot, Justin O., Carla Campagnolo, Ye Cao, et al.. (2019). Bi-allelic Mutations in NADSYN1 Cause Multiple Organ Defects and Expand the Genotypic Spectrum of Congenital NAD Deficiency Disorders. The American Journal of Human Genetics. 106(1). 129–136. 30 indexed citations
9.
Arian, Sara E., et al.. (2017). Genetic screening and testing in pregnancies conceived by in vitro fertilization (IVF) with preimplantation genetic screening (PGS). Fertility and Sterility. 108(3). e292–e292. 3 indexed citations
10.
11.
Westerfield, Lauren, Sandra Darilek, & Ignatia Van den Veyver. (2014). Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis. Journal of Clinical Medicine. 3(3). 1018–1032. 56 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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2026