Jennifer Malinowski

2.5k total citations · 3 hit papers
30 papers, 1.1k citations indexed

About

Jennifer Malinowski is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Jennifer Malinowski has authored 30 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 7 papers in Pediatrics, Perinatology and Child Health and 4 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Jennifer Malinowski's work include Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (6 papers) and BRCA gene mutations in cancer (5 papers). Jennifer Malinowski is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (6 papers) and BRCA gene mutations in cancer (5 papers). Jennifer Malinowski collaborates with scholars based in United States, Canada and Australia. Jennifer Malinowski's co-authors include Monica R. McClain, Laurie Demmer, Timothy W. Yu, Lauren Massingham, Danny E. Miller, Sawona Biswas, Kandamurugu Manickam, Fuki M. Hisama, Hutton M. Kearney and Beth Rosen Sheidley and has published in prestigious journals such as PLoS ONE, Epilepsia and BMC Medicine.

In The Last Decade

Jennifer Malinowski

29 papers receiving 1.0k citations

Hit Papers

Exome and genome sequencing for pediatric patients with c... 2021 2026 2022 2024 2021 2022 2022 50 100 150 200 250
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
    2021 288 citations Kandamurugu Manickam, Monica R. McClain et al. Genetics in Medicine profile →
  2. Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
    2022 101 citations J.S. Dungan, Susan Klugman et al. Genetics in Medicine profile →
  3. Trends in guideline implementation: an updated scoping review
    2022 71 citations Sanne Peters, Scott C. Blanchard et al. Implementation Science profile →

Peers

Jennifer Malinowski
Tommaso Aversa Italy
J.M. Wit Netherlands
Katherine S. Ruth United Kingdom
Jean Morrison United States
Marcus A. Tuke United Kingdom
Kristina Gervin Norway
Yaqin Zhang China
C. Volta Italy
M Vanelli Italy
Despoina Manousaki Canada
Tommaso Aversa Italy
Jennifer Malinowski
Citations per year, relative to Jennifer Malinowski Jennifer Malinowski (= 1×) peers Tommaso Aversa

Countries citing papers authored by Jennifer Malinowski

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer Malinowski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jennifer Malinowski

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

All Works

20 of 20 papers shown
1.
Smith, Wendy E., Susan A. Berry, Christine Brown, et al.. (2024). Phenylalanine hydroxylase deficiency diagnosis and management: A 2023 evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 27(1). 101289–101289. 10 indexed citations
2.
Schwartz, M., Miranda L. G. Hallquist, Yirui Hu, et al.. (2024). Genetics Visit Uptake Among Individuals Receiving Clinically Actionable Genomic Screening Results. JAMA Network Open. 7(3). e242388–e242388. 3 indexed citations
3.
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
4.
5.
Smith, Lacey, et al.. (2022). Genetic testing and counseling for the unexplained epilepsies: An evidence‐based practice guideline of the National Society of Genetic Counselors. Journal of Genetic Counseling. 32(2). 266–280. 52 indexed citations
6.
Dungan, J.S., Susan Klugman, Sandra Darilek, et al.. (2022). Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 25(2). 100336–100336. 101 indexed citations breakdown →
7.
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
8.
Savatt, Juliann M., Melissa Kelly, Alexander S. F. Berry, et al.. (2022). Observational study of population genomic screening for variants associated with endocrine tumor syndromes in a large, healthcare-based cohort. BMC Medicine. 20(1). 205–205. 6 indexed citations
9.
Peters, Sanne, Scott C. Blanchard, Jennifer Malinowski, et al.. (2022). Trends in guideline implementation: an updated scoping review. Implementation Science. 17(1). 50–50. 71 indexed citations breakdown →
10.
Sheidley, Beth Rosen, Jennifer Malinowski, Amanda L. Bergner, et al.. (2021). Genetic testing for the epilepsies: A systematic review. Epilepsia. 63(2). 375–387. 67 indexed citations
11.
Cook, Lola, et al.. (2021). Telehealth for genetic counseling: A systematic evidence review. Journal of Genetic Counseling. 30(5). 1361–1378. 46 indexed citations
12.
Malinowski, Jennifer, et al.. (2021). Sysrev: A FAIR Platform for Data Curation and Systematic Evidence Review. Frontiers in Artificial Intelligence. 4. 685298–685298. 61 indexed citations
13.
Manickam, Kandamurugu, Monica R. McClain, Laurie Demmer, et al.. (2021). Exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability: an evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 23(11). 2029–2037. 288 indexed citations breakdown →
14.
Malinowski, Jennifer, David T. Miller, Laurie Demmer, et al.. (2020). Systematic evidence-based review: outcomes from exome and genome sequencing for pediatric patients with congenital anomalies or intellectual disability. Genetics in Medicine. 22(6). 986–1004. 52 indexed citations
15.
Chen, Aleda M.H., Jaime Maerten‐Rivera, Jennifer Malinowski, et al.. (2020). Administration and Evaluation of the American Association of Colleges of Pharmacy Curriculum Quality Surveys in Pharmacy Schools. American Journal of Pharmaceutical Education. 85(3). 8045–8045. 3 indexed citations
16.
Callender, Glenda G., Jennifer Malinowski, Yawei Zhang, et al.. (2016). Parathyroidectomy prior to kidney transplant decreases graft failure. Surgery. 161(1). 44–50. 34 indexed citations
17.
Malinowski, Jennifer, et al.. (2016). Dissection of Levels II Through V Is Required for Optimal Outcomes in Patients with Lateral Neck Lymph Node Metastasis from Papillary Thyroid Carcinoma. Journal of the American College of Surgeons. 222(6). 1066–1073. 35 indexed citations
18.
19.
Spencer, Kylee L., Jennifer Malinowski, Cara L. Carty, et al.. (2013). Genetic Variation and Reproductive Timing: African American Women from the Population Architecture Using Genomics and Epidemiology (PAGE) Study. PLoS ONE. 8(2). e55258–e55258. 33 indexed citations
20.
Malinowski, Jennifer, et al.. (2010). Original research Vasopressor choice for hypotension in elective Cesarean section: ephedrine or phenylephrine?. Archives of Medical Science. 2(2). 257–263. 20 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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