Sandra Darilek

1.4k total citations · 1 hit paper
24 papers, 780 citations indexed

About

Sandra Darilek is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Sandra Darilek has authored 24 papers receiving a total of 780 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Pediatrics, Perinatology and Child Health, 10 papers in Genetics and 6 papers in Molecular Biology. Recurrent topics in Sandra Darilek's work include Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Sandra Darilek is often cited by papers focused on Prenatal Screening and Diagnostics (14 papers), Genomic variations and chromosomal abnormalities (6 papers) and Fetal and Pediatric Neurological Disorders (5 papers). Sandra Darilek collaborates with scholars based in United States and Canada. Sandra Darilek's co-authors include Patricia A. Ward, Sau Wai Cheung, Christine M. Eng, Ankita Patel, Ignatia Van den Veyver, Lauren Westerfield, Amber N. Pursley, Ignatia B. Van den Veyver, Arthur L. Beaudet and Chad A. Shaw and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genome Research and American Journal of Obstetrics and Gynecology.

In The Last Decade

Sandra Darilek

23 papers receiving 731 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

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 101 citations J.S. Dungan, Susan Klugman et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Sandra Darilek United States	13	516	456	198	66	49	24	780
Kamal K. Naguib Kuwait	14	140 0.3×	269 0.6×	189 1.0×	9 0.1×	37 0.8×	40	558
Christopher McCaskill United States	16	397 0.8×	672 1.5×	296 1.5×	7 0.1×	127 2.6×	22	825
J Lejeune France	14	163 0.3×	328 0.7×	202 1.0×	21 0.3×	99 2.0×	50	576
Dunja Niedrist Switzerland	8	119 0.2×	279 0.6×	263 1.3×	6 0.1×	37 0.8×	11	571
Lutgarde Govaerts Netherlands	16	459 0.9×	441 1.0×	191 1.0×	5 0.1×	20 0.4×	32	723
Sue Ann Berend United States	15	336 0.7×	432 0.9×	174 0.9×	6 0.1×	149 3.0×	20	584
Sally Rosengren United States	9	90 0.2×	207 0.5×	293 1.5×	132 2.0×	10 0.2×	15	665
Kenneth L. Garver United States	11	225 0.4×	260 0.6×	160 0.8×	6 0.1×	42 0.9×	24	712
Lisskulla Sylvén Sweden	10	53 0.1×	455 1.0×	231 1.2×	34 0.5×	36 0.7×	12	653
Kwang-Jen Hsiao Taiwan	14	177 0.3×	87 0.2×	279 1.4×	13 0.2×	10 0.2×	37	667

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-authorship network of co-authors of Sandra Darilek

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

All Works

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20 of 20 papers shown

Ball, Robert, et al.. (2024). Telegenetics to provide comprehensive prenatal diagnosis. Prenatal Diagnosis. 44(4). 492–498.

Dungan, J.S., Susan Klugman, Sandra Darilek, et al.. (2022). 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). Genetics in Medicine. 25(2). 100336–100336. 101 indexed citations breakdown →

Azamian, Mahshid S., et al.. (2021). A rare description of pure partial trisomy of 16q12.2q24.3 and review of the literature. American Journal of Medical Genetics Part A. 185(10). 2903–2912. 2 indexed citations

Alkhunaizi, Ebba, Patrick Shannon, Victoria Mok Siu, et al.. (2019). Homozygous/compound heterozygote RYR1 gene variants: Expanding the clinical spectrum. American Journal of Medical Genetics Part A. 179(3). 386–396. 14 indexed citations

Darilek, Sandra, et al.. (2018). 267: Pregnancy outcome following transfer of an aneuploid embryo. American Journal of Obstetrics and Gynecology. 218(1). S170–S170. 3 indexed citations

Allyse, Megan, Umut Aypar, Natasha Bonhomme, et al.. (2017). Offering Prenatal Screening in the Age of Genomic Medicine: A Practical Guide. Journal of Women s Health. 26(7). 755–761. 9 indexed citations

McGuire, Amy L., Quianta Moore, Mary A. Majumder, et al.. (2016). The ethics of conducting molecular autopsies in cases of sudden death in the young. Genome Research. 26(9). 1165–1169. 13 indexed citations

Kohn, Taylor P., Jaden R. Kohn, Sandra Darilek, Ranjith Ramasamy, & Larry I. Lipshultz. (2016). Genetic counseling for men with recurrent pregnancy loss or recurrent implantation failure due to abnormal sperm chromosomal aneuploidy. Journal of Assisted Reproduction and Genetics. 33(5). 571–576. 33 indexed citations

Fang, Ping, Jerry Lin, Sandra Darilek, et al.. (2015). DNA sequence analysis and genotype–phenotype assessment in 71 patients with syndromic hearing loss or auditory neuropathy. BMJ Open. 5(5). e007506–e007506. 10 indexed citations

10.

Turrentine, Mark, et al.. (2015). Obstetrician and Gynecologist Utilization of the Noninvasive Prenatal Testing Expanded Option. SHILAP Revista de lepidopterología. 6(1). e18–e24. 5 indexed citations

11.

Westerfield, Lauren, Sandra Darilek, & Ignatia Van den Veyver. (2014). Counseling Challenges with Variants of Uncertain Significance and Incidental Findings in Prenatal Genetic Screening and Diagnosis. Journal of Clinical Medicine. 3(3). 1018–1032. 56 indexed citations

12.

Alford, Raye Lynn & Sandra Darilek. (2011). Basic Medical Genetics for the Otolaryngologist. Advances in oto-rhino-laryngology. 70. 10–17. 1 indexed citations

13.

Brandt, Amanda, Matthew L. Tschirgi, Kaylene Ready, et al.. (2010). Knowledge, attitudes, and clinical experience of physicians regarding preimplantation genetic diagnosis for hereditary cancer predisposition syndromes. Familial Cancer. 9(3). 479–487. 27 indexed citations

14.

Veyver, Ignatia B. Van den, Ankita Patel, Chad A. Shaw, et al.. (2008). Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases. Prenatal Diagnosis. 29(1). 29–39. 155 indexed citations

15.

Darilek, Sandra, Patricia A. Ward, Amber N. Pursley, et al.. (2008). Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives. Genetics in Medicine. 10(1). 13–18. 64 indexed citations

16.

Basehore, Monica J., Sandra Darilek, John S. Oghalai, et al.. (2008). Infrequency of two deletion mutations at the DFNB1 locus in patients and controls. American Journal of Medical Genetics Part A. 146A(7). 934–936. 2 indexed citations

17.

Cooper, M. Lance, et al.. (2006). A retrospective study of preimplantation embryos diagnosed with monosomy by fluorescence in situ hybridization (FISH). Cytogenetic and Genome Research. 114(3-4). 359–366. 9 indexed citations

18.

Fang, Ping, Patricia A. Ward, Eric Schmitt, et al.. (2006). DNA sequence analysis of GJB2, encoding connexin 26: Observations from a population of hearing impaired cases and variable carrier rates, complex genotypes, and ethnic stratification of alleles among controls. American Journal of Medical Genetics Part A. 140A(22). 2401–2415. 60 indexed citations

19.

Sahoo, Trilochan, Sau Wai Cheung, Patricia A. Ward, et al.. (2006). Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization. Genetics in Medicine. 8(11). 719–727. 128 indexed citations

20.

Darilek, Sandra, Diane M. Novy, Allison M. Scott, et al.. (2005). Hereditary Multiple Exostosis and Pain. Journal of Pediatric Orthopaedics. 25(3). 369–376. 45 indexed citations

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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