Julia Platt

1.1k citations
13 papers · 333 · h-index 10

Impact in

    • Genomics and Rare Diseases
    • BRCA gene mutations in cancer
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Metabolism and Genetic Disorders

Papers in

    • Genomics and Rare Diseases 4
    • BRCA gene mutations in cancer 3
    • Genetics and Neurodevelopmental Disorders 1
    • Mitochondrial Function and Pathology 2

Julia Platt

12 papers receiving 323 citations

Peers

Julia Platt
Comparison fields: 5 of 57
  • Genetics 133
  • Clinical Biochemistry 31
  • Neurology 41
  • Neurology 23
  • Molecular Biology 129
Replace Miguel Leão with:
Miguel Leão Portugal
Juliette Piard France
Jane Fleming Australia
Filip Roelens Belgium
Sandra Whalen France
Tatjana Bierhals Germany
Rony Cohen Israel
Tiia Reimand Estonia
Kelly D. Farwell Hagman United States
Melissa T. Carter Canada
Julia Platt relative to Miguel Leão Portugal Miguel Leão's profile →
Citations per field
00.5×1.5×1.9×
Miguel Leão · 1×
Citations per year

Countries citing papers authored by Julia Platt

Since Specialization
Citations

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

Fields of papers citing papers by Julia Platt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Julia Platt, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Julia Platt Line = papers co-authored together Julia Platt links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1 201284
2 201446
3 201242
4
Growth and development of children with X and Y chromosome aneuploidy: a prospective study.
197938
5 201738
6 201523
7 201414
8 202013
9 201113
10 199113
11 20198
12 20241
13 20250

About Julia Platt

Julia Platt is a scholar working on Genetics, Molecular Biology, Genetics, Cardiology and Cardiovascular Medicine and Clinical Biochemistry, having authored 13 papers that have together received 333 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (4 papers), BRCA gene mutations in cancer (3 papers), Metabolism and Genetic Disorders (2 papers), Mitochondrial Function and Pathology (2 papers), Chronic Myeloid Leukemia Treatments (1 paper), Amyotrophic Lateral Sclerosis Research (1 paper), Genetics and Neurodevelopmental Disorders (1 paper) and Childhood Cancer Survivors' Quality of Life (1 paper). The work is most often cited by research in Genetics (133 citations), Clinical Biochemistry (31 citations), Neurology (41 citations), Neurology (23 citations) and Molecular Biology (129 citations). Julia Platt has collaborated with scholars based in United States, United Kingdom and Japan. Frequent co-authors include Gregory M. Enns, Michael V. Zaragoza, Eric Dec, Jonathan A. Bernstein, R. Ramani, Angèle Nalbandian, Rachel Cox, Mariella Simon, Manaswitha Khare and Sandra Donkervoort. Their work appears in journals such as Genetics in Medicine, Mitochondrion, Molecular Genetics and Metabolism, Clinical Genetics and Annals of Hematology.

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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