Sandra Darilek

1.4k citations
24 papers · 796 · 1 hit paper · h-index 13

Impact in

Papers in

    • Prenatal Screening and Diagnostics 14
    • Assisted Reproductive Technology and Twin Pregnancy 3
    • Fetal and Pediatric Neurological Disorders 2
    • BRCA gene mutations in cancer 4
    • Genomic variations and chromosomal abnormalities 4

Sandra Darilek

23 papers receiving 747 citations

Sandra Darilek's Hit Papers

Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG) 2022 · 110 citations
1100+1+2Years since publication255075100

Peers

Sandra Darilek
Comparison fields: 5 of 58
  • Pediatrics, Perinatology and Child Health 474
  • Sensory Systems 61
  • Genetics 317
  • Oral Surgery 21
  • Rheumatology 42
Replace Young Ho Yang with:
Young Ho Yang South Korea
Sue Ann Berend United States
J Lejeune France
Kenneth L. Garver United States
Lisskulla Sylvén Sweden
Lutgarde Govaerts Netherlands
Alison Lashwood United Kingdom
Alvaro Mesoraca Italy
Philip D. Pallister United States
Karen Fieggen South Africa
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Citations per field
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Citations per year

Countries citing papers authored by Sandra Darilek

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Darilek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 24 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2008156
2 2006128
3
Noninvasive prenatal screening (NIPS) for fetal chromosome abnormalities in a general-risk population: An evidence-based clinical guideline of the American College of Medical Genetics and Genomics (ACMG)
Hit paper breakdown →
2022110
4 200864
5 200661
6 201458
7 200544
8 201633
9 201027
10 201621
11 201615
12 201914
13 201813
14 201510
15 20069
16 20179
17 20188
18 20155
19 20213
20 20183

About Sandra Darilek

Sandra Darilek is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Molecular Biology, Sensory Systems and Surgery, having authored 24 papers that have together received 796 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (14 papers), BRCA gene mutations in cancer (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Assisted Reproductive Technology and Twin Pregnancy (3 papers), Fetal and Pediatric Neurological Disorders (2 papers), Congenital heart defects research (2 papers), Hearing, Cochlea, Tinnitus, Genetics (2 papers) and Musculoskeletal synovial abnormalities and treatments (1 paper). The work is most often cited by research in Pediatrics, Perinatology and Child Health (474 citations), Sensory Systems (61 citations), Genetics (317 citations), Oral Surgery (21 citations) and Rheumatology (42 citations). Sandra Darilek has collaborated with scholars based in United States and Canada. Frequent co-authors include Patricia A. Ward, Christine M. Eng, Sau Wai Cheung, Ankita Patel, Lauren Westerfield, Ignatia Van den Veyver, Amber N. Pursley, Chad A. Shaw, Ignatia B. Van den Veyver and Arthur L. Beaudet. Their work appears in journals such as Genetics in Medicine, Prenatal Diagnosis, American Journal of Obstetrics and Gynecology, Journal of Assisted Reproduction and Genetics and Journal of Pediatric Orthopaedics.

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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