Anna Newlin

1.9k citations
17 papers · 425 indexed · h-index 12

Impact in

  • Genetics top 10%
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • BRCA gene mutations in cancer 4
    • Genomics and Rare Diseases 3
    • Genomic variations and chromosomal abnormalities 3
    • Cancer and Skin Lesions 3

Anna Newlin

16 papers receiving 406 citations

Peers

Anna Newlin
Comparison fields: 5 of 43
  • Genetics 210
  • Ophthalmology 64
  • Pediatrics, Perinatology and Child Health 96
  • Reproductive Medicine 37
  • Developmental Neuroscience 14
Replace Hadia Hijazi with:
Hadia Hijazi Saudi Arabia
Kristin Bosse Germany
Tom Sante Belgium
Carmelilia De Bernardo Italy
Anita S. Kulharya United States
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Citations per field
00.5×4.7×
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Citations per year

Countries citing papers authored by Anna Newlin

Since Specialization
Citations

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

Fields of papers citing papers by Anna Newlin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

17 of 17 papers shown
#Work
1 199299
2 200453
3 199952
4 201239
5 199931
6 201429
7 200724
8 201222
9 199021
10 200817
11 199616
12 200612
13 19994
14 20163
15 19932
16 20181
17 20220

About Anna Newlin

Anna Newlin is a scholar working on Genetics, Dermatology, Ophthalmology, Pathology and Forensic Medicine and Pediatrics, Perinatology and Child Health, having authored 17 papers that have together received 425 indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (5 papers), BRCA gene mutations in cancer (4 papers), Prenatal Screening and Diagnostics (3 papers), Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Cancer and Skin Lesions (3 papers), Colorectal Cancer Treatments and Studies (2 papers) and Glaucoma and retinal disorders (2 papers). The work is most often cited by research in Genetics (210 citations), Ophthalmology (64 citations), Pediatrics, Perinatology and Child Health (96 citations), Reproductive Medicine (37 citations) and Developmental Neuroscience (14 citations). Anna Newlin has collaborated with scholars based in United States and Canada. Frequent co-authors include William B. Dobyns, Ellen Roy Elias, David H. Ledbetter, Scott M. Weissman, Joel Sugar, Kristen J. Vogel, Barbara K. Burton, Timothy T. McMahon, Julie A. Shin and Marilyn T. Miller. Their work appears in journals such as Familial Cancer, Cornea, Ophthalmology, Frontiers in Genetics and JCO Precision Oncology.

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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