Diane Masser‐Frye

1.1k total citations
6 papers, 243 citations indexed

About

Diane Masser‐Frye is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Hematology. According to data from OpenAlex, Diane Masser‐Frye has authored 6 papers receiving a total of 243 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Pediatrics, Perinatology and Child Health and 2 papers in Hematology. Recurrent topics in Diane Masser‐Frye's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Pregnancy and preeclampsia studies (1 paper). Diane Masser‐Frye is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (2 papers) and Pregnancy and preeclampsia studies (1 paper). Diane Masser‐Frye collaborates with scholars based in United States, Japan and Canada. Diane Masser‐Frye's co-authors include Maureen Bocian, Moyra Smith, Pauline A. Filipek, M. Anne Spence, J. Jay Gargus, Tracy M. Laulhere, Charlotte Modahl, Kathryn L. Berrier, Cori Feist and Blythe G. Crissman and has published in prestigious journals such as Annals of Neurology, The American Journal of Human Genetics and Prenatal Diagnosis.

In The Last Decade

Diane Masser‐Frye

6 papers receiving 226 citations

Peers

Diane Masser‐Frye

GENET

PPCH

MB

CN

CP

Loretta Thomaidis Greece

Anita J. Hughes United Kingdom

Silvia Sacco France

Watfa Al‐Mamari Oman

Lucy Wilde United Kingdom

Elisabeth Siti Herini Indonesia

Stephanie J. Brewster United States

Nada A. Elsayed United States

Bonnie Patterson United States

Loretta Thomaidis Greece

Diane Masser‐Frye

205 ×2.2

GENET

105 ×1.3

PPCH

128 ×1.6

MB

84 ×1.1

CN

47 ×1.4

CP

Citations per year, relative to Diane Masser‐Frye Diane Masser‐Frye (= 1×) peers Loretta Thomaidis

Countries citing papers authored by Diane Masser‐Frye

Since Specialization

Citations

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

Fields of papers citing papers by Diane Masser‐Frye

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Diane Masser‐Frye. 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 Diane Masser‐Frye. The network helps show where Diane Masser‐Frye may publish in the future.

Co-authorship network of co-authors of Diane Masser‐Frye

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

All Works

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6 of 6 papers shown

1.

Masser‐Frye, Diane, et al.. (2020). The odds and implications of coinheritance of hemophilia A and B. Research and Practice in Thrombosis and Haemostasis. 4(5). 931–935. 4 indexed citations

2.

Campo, Miguel Del, et al.. (2020). Acute Megakaryoblastic Leukemia Leading to the Diagnosis of Germline Trisomy 21 Mosaicism. Journal of Pediatric Hematology/Oncology. 42(4). 299–301. 1 indexed citations

3.

Nguyen, Thi Tuyet Mai, Yoshiko Murakami, Kristen Wigby, et al.. (2018). Mutations in PIGS, Encoding a GPI Transamidase, Cause a Neurological Syndrome Ranging from Fetal Akinesia to Epileptic Encephalopathy. The American Journal of Human Genetics. 103(4). 602–611. 40 indexed citations

4.

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

5.

Filipek, Pauline A., Moyra Smith, Maureen Bocian, et al.. (2003). Mitochondrial dysfunction in autistic patients with 15q inverted duplication. Annals of Neurology. 53(6). 801–804. 109 indexed citations

6.

Bird, Lynne M., Diane Masser‐Frye, Lluís Ribas-Xirgo, et al.. (2002). Choroid plexus cysts in the mid‐trimester fetus—practical application suggests superiority of an individualized risk method of counseling for trisomy 18. Prenatal Diagnosis. 22(9). 792–797. 5 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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