Mary Willis

1.3k citations
17 papers · 369 · h-index 10

Impact in

    • Metabolism and Genetic Disorders
  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Genomics and Rare Diseases

Papers in

    • Genomic variations and chromosomal abnormalities 3
    • Genomics and Rare Diseases 3
    • Genetics and Neurodevelopmental Disorders 2
    • Hedgehog Signaling Pathway Studies 2
    • Biochemical and Molecular Research 2

Mary Willis

16 papers receiving 343 citations

Peers

Mary Willis
Comparison fields: 5 of 56
  • Clinical Biochemistry 62
  • Genetics 176
  • Developmental Biology 6
  • Pediatrics, Perinatology and Child Health 45
  • Molecular Biology 176
Replace Marie McDonald with:
Marie McDonald United States
Sandesh C. Sreenath Nagamani United States
Kelly E. Jackson United States
Sue Forrest Australia
Michèle Mathieu‐Dramard France
Mahmoud Taleb Al‐Ali United Arab Emirates
Jostein Westvik Norway
Ligia Mateiu Belgium
Ho‐Ming Luk China
Maria Tereza Matias Baptista Brazil
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Citations per field
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Citations per year

Countries citing papers authored by Mary Willis

Since Specialization
Citations

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

Fields of papers citing papers by Mary Willis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Mary Willis, 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 Mary Willis Line = papers co-authored together Mary Willis links everyone, so they are left out of the graph.

All Works

17 of 17 papers shown
#Work
1 201596
2 200845
3 201442
4 200841
5 200632
6 200824
7 201120
8 201320
9 202015
10 201215
11 20226
12 19824
13 20234
14 20233
15 20151
16 20231
17 20060

About Mary Willis

Mary Willis is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Surgery, having authored 17 papers that have together received 369 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Genomics and Rare Diseases (3 papers), Prenatal Screening and Diagnostics (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Metabolism and Genetic Disorders (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Biochemical and Molecular Research (2 papers) and Muscle metabolism and nutrition (1 paper). The work is most often cited by research in Clinical Biochemistry (62 citations), Genetics (176 citations), Developmental Biology (6 citations), Pediatrics, Perinatology and Child Health (45 citations) and Molecular Biology (176 citations). Mary Willis has collaborated with scholars based in United States, Canada and Brazil. Frequent co-authors include Lynne M. Bird, Marilyn C. Jones, Sibel Kantarci, Andrea Kwan, Paul J. Isackson, Samuel P. Strom, Melanie A. Manning, Stanley F. Nelson, Uta Lichter‐Konecki and Georgirene D. Vladutiu. Their work appears in journals such as Molecular Genetics and Metabolism, European Journal of Medical Genetics, Prenatal Diagnosis, Schizophrenia Bulletin and Journal of Investigative Medicine.

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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