Laura S. Farach

650 citations
22 papers · 127 indexed · h-index 7
    • Genetics and Neurodevelopmental Disorders 6
    • Genomic variations and chromosomal abnormalities 3
    • Genetic Syndromes and Imprinting 2
    • Genomics and Rare Diseases 2
    • RNA modifications and cancer 3
    • Tuberous Sclerosis Complex Research 4
    • Genetics and Neurodevelopmental Disorders 6
    • Genomic variations and chromosomal abnormalities 3
    • Genetic Syndromes and Imprinting 2
    • Genomics and Rare Diseases 2
    • Metabolism and Genetic Disorders 3
    • Polyomavirus and related diseases 3

Laura S. Farach

19 papers receiving 127 citations

Peers

Laura S. Farach
Comparison fields: 5 of 39
  • Genetics 57
  • Molecular Biology 71
  • Physiology 20
  • Cognitive Neuroscience 14
  • Genetics 7
Replace Lea Velsher with:
Lea Velsher Canada
Rebecca Willaert United States
Jillene Kogan United States
Connie T. R. M. Stumpel Netherlands
Elly Brokamp United States
Haley Streff United States
Yannis Duffourd France
Gabrielle Lemire Canada
Fabio Sirchia Italy
Salima El Chehadeh-Djebbar France
Laura S. Farach relative to Lea Velsher Canada Lea Velsher's profile →
Citations per field
00.5×2.7×
Lea Velsher · 1×
Citations per year

Countries citing papers authored by Laura S. Farach

Since Specialization
Citations

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

Fields of papers citing papers by Laura S. Farach

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Laura S. Farach. 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 Laura S. Farach. The network helps show where Laura S. Farach may publish in the future.

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20251
2 20241
3 20231
4 20230
5 20233
6 20223
7 20220
8 20223
9 20220
10 20225
11 20213
12 20213
13 20202
14 20204
15 20196
16 201914
17 20186
18 201711
19 201518
20 20136

About Laura S. Farach

Laura S. Farach is a scholar working on Genetics, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 22 papers that have together received 127 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Tuberous Sclerosis Complex Research (4 papers), Metabolism and Genetic Disorders (3 papers), Genomic variations and chromosomal abnormalities (3 papers), Polyomavirus and related diseases (3 papers), RNA modifications and cancer (3 papers), Genetic Syndromes and Imprinting (2 papers) and Genomics and Rare Diseases (2 papers). The work is most often cited by research in Genetics (57 citations), Molecular Biology (71 citations) and Physiology (20 citations). Laura S. Farach has collaborated with scholars based in United States, Netherlands and United Kingdom. Frequent co-authors include Hope Northrup, Michael B. Bober, Andrew P. Jackson, Angela L. Duker, Clare V. Logan, Joseph W. Ray, Kate Mowrey, S. Shahrukh Hashmi, Andrew Farach and Deborah A. Pearson. Their work appears in journals such as SHILAP Revista de lepidopterología, Gene and Frontiers in Genetics.

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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