Sandra Peacock

1.1k total citations
11 papers, 489 citations indexed

About

Sandra Peacock is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Sandra Peacock has authored 11 papers receiving a total of 489 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in Sandra Peacock's work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Sandra Peacock is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Sandra Peacock collaborates with scholars based in United States and Brazil. Sandra Peacock's co-authors include Sau Wai Cheung, Janice Smith, Amy M. Breman, Ignatia B. Van den Veyver, Patricia A. Ward, Andrea Petersen, Weimin Bi, Alicia Braxton, Ankita Patel and Paweł Stankiewicz and has published in prestigious journals such as Human Molecular Genetics, American Journal of Obstetrics and Gynecology and The Journal of Urology.

In The Last Decade

Sandra Peacock

11 papers receiving 482 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandra Peacock United States	9	308	207	183	71	58	11	489
Sandra Darilek United States	13	456 1.5×	516 2.5×	198 1.1×	49 0.7×	31 0.5×	24	780
G. Lefort France	16	377 1.2×	290 1.4×	189 1.0×	217 3.1×	33 0.6×	34	632
E. J. Maher United Kingdom	8	440 1.4×	342 1.7×	173 0.9×	129 1.8×	28 0.5×	11	613
Ioannis Papoulidis Greece	13	251 0.8×	195 0.9×	116 0.6×	51 0.7×	24 0.4×	52	388
Dehua Cheng China	12	300 1.0×	307 1.5×	242 1.3×	67 0.9×	16 0.3×	44	618
Chiara Palka Italy	10	210 0.7×	136 0.7×	255 1.4×	36 0.5×	24 0.4×	34	468
Laïla El Khattabi France	11	133 0.4×	131 0.6×	156 0.9×	25 0.4×	37 0.6×	25	343
Neus Baena Spain	13	286 0.9×	199 1.0×	132 0.7×	43 0.6×	18 0.3×	31	470
Anne M. Bandholz United States	6	355 1.2×	332 1.6×	154 0.8×	20 0.3×	37 0.6×	8	515
Nathalie Leporrier France	15	167 0.5×	251 1.2×	153 0.8×	34 0.5×	62 1.1×	24	478

Countries citing papers authored by Sandra Peacock

Since Specialization

Citations

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

Fields of papers citing papers by Sandra Peacock

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Peacock

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

All Works

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11 of 11 papers shown

Lemoine, Jean, Paul R. Billings, Sandra Peacock, et al.. (2021). Clinical experience with non‐invasive prenatal screening for single‐gene disorders. Ultrasound in Obstetrics and Gynecology. 59(1). 33–39. 43 indexed citations

Cao, Ye, Yanjun Jiang, Sandra Peacock, et al.. (2018). 930: Clinical utility of non-invasive prenatal screening for common dominant monogenic disorders. American Journal of Obstetrics and Gynecology. 220(1). S599–S599. 1 indexed citations

Gu, Shen, et al.. (2018). Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions. Prenatal Diagnosis. 38(11). 858–865. 13 indexed citations

Petersen, Andrea, Sau Wai Cheung, Janice Smith, et al.. (2017). Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory. American Journal of Obstetrics and Gynecology. 217(6). 691.e1–691.e6. 127 indexed citations

Wang, Jing, Victor Wei Zhang, Tian Xia, et al.. (2015). Capture-based high-coverage NGS: a powerful tool to uncover a wide spectrum of mutation types. Genetics in Medicine. 18(5). 513–521. 21 indexed citations

Raju, S. Vamsee, Sandra Peacock, Ping Fang, et al.. (2014). Impact of heterozygote CFTR Mutations in COPD patients with Chronic Bronchitis. Respiratory Research. 15(1). 18–18. 33 indexed citations

Gu, Jun, Sandesh C. Sreenath Nagamani, Vicki L. Hopwood, et al.. (2011). Complex genomic rearrangement of chromosome 16p13.3 detected by array comparative genomic hybridization in a patient with multiple congenital anomalies, dysmorphic craniofacial features, and developmental delay. American Journal of Medical Genetics Part A. 155(10). 2589–2592. 1 indexed citations

Yatsenko, Alexander N., Svetlana A. Yatsenko, John Weedin, et al.. (2010). Comprehensive 5-Year Study of Cytogenetic Aberrations in 668 Infertile Men. The Journal of Urology. 183(4). 1636–1642. 45 indexed citations

Carvalho, Claudia M.B., Feng Zhang, Pengfei Liu, et al.. (2009). Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching. Human Molecular Genetics. 18(12). 2188–2203. 146 indexed citations

10.

Schuette, Jane L., et al.. (2009). Identification of critical regions for clinical features of distal 10q deletion syndrome. Clinical Genetics. 76(1). 54–62. 48 indexed citations

11.

Shchelochkov, Oleg A., M. Lance Cooper, Zhishuo Ou, et al.. (2008). Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement. Molecular Cytogenetics. 1(1). 16–16. 11 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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