Natalia T. Leach

1.5k citations
17 papers · 587 indexed · 2 hit papers · h-index 9
Topics
Genomic variations and chromosomal abnormalities (8 papers)Genomics and Rare Diseases (4 papers)Prenatal Screening and Diagnostics (4 papers)

In The Last Decade

Natalia T. Leach

16 papers receiving 577 citations

Hit Papers

Screening for autosomal recessive and X-linked conditions...20202026202220242021202050100150200

Peers

Natalia T. Leach
Comparison fields: 5 of 71
  • Genetics 264
  • Pediatrics, Perinatology and Child Health 245
  • Molecular Biology 199
  • Pulmonary and Respiratory Medicine 113
  • Cancer Research 62
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Natalia T. Leach relative to Mahmoud Aarabi United States Mahmoud Aarabi's profile →
Citations per field
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Mahmoud Aarabi · 1×
Citations per year

Countries citing papers authored by Natalia T. Leach

Since Specialization
Citations

This map shows the geographic impact of Natalia T. Leach'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 Natalia T. Leach with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Natalia T. Leach more than expected).

Fields of papers citing papers by Natalia T. Leach

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Natalia T. Leach. 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 Natalia T. Leach. The network helps show where Natalia T. Leach may publish in the future.

Co-authorship network of co-authors of Natalia T. Leach

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

All Works

17 of 17 papers shown
#WorkIndexed citations
1 0
2 2
3 2
4 2
5 9
6
Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)breakdown →
221
7
The use of fetal exome sequencing in prenatal diagnosis: a points to consider document of the American College of Medical Genetics and Genomics (ACMG)breakdown →
157
8 3
9 5
10 15
11 15
12 39
13 3
14 43
15 1
16 33
17 37

About Natalia T. Leach

Natalia T. Leach is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Urology, having authored 17 papers that have together received 587 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (4 papers) and Prenatal Screening and Diagnostics (4 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (245 citations), Genetics (264 citations) and Cancer Research (62 citations). Natalia T. Leach has collaborated with scholars based in United States, Canada and Australia. Frequent co-authors include Colleen Jackson‐Cook, Priya Prasad, Nancy C. Rose, Kristin G. Monaghan, Anthony R. Gregg, Aleksandar Rajkovic, J.S. Dungan, Teresa N. Sparks, Emily Chen and Susan Klugman. Their work appears in journals such as New England Journal of Medicine, Scientific Reports and The American Journal of Human 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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