Sandra Peacock

1.1k citations

11 papers · 489 indexed · h-index 9

Genetics top 10%
Pediatrics, Perinatology and Child Health top 5%
Molecular Biology
Plant Science
Infectious Diseases

Co-authors: Sau Wai Cheung Janice Smith Amy M. Breman Ignatia B. Van den Veyver Patricia A. Ward Andrea Petersen Weimin Bi Alicia Braxton
Topics: Genomic variations and chromosomal abnormalities (7 papers)Prenatal Screening and Diagnostics (5 papers)Genetics and Neurodevelopmental Disorders (3 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Reproductive Medicine
Journals: Human Molecular Genetics American Journal of Obstetrics and Gynecology The Journal of Urology
Partner nations: United States Brazil

In The Last Decade

Sandra Peacock

11 papers receiving 482 citations

Peers

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

#	Work	Indexed citations
1	Clinical experience with non‐invasive prenatal screening for single‐gene disorders 2021 ·Ultrasound in Obstetrics and Gynecology ·(unknown),Jean Lemoine,(unknown),(unknown),Paul R. Billings,Sandra Peacock,(unknown),Y. Wang,Fan Xia,Christine M. Eng,Peter Benn	43
2	930: Clinical utility of non-invasive prenatal screening for common dominant monogenic disorders 2018 ·American Journal of Obstetrics and Gynecology ·Ye Cao,Yanjun Jiang,(unknown),Sandra Peacock,Eric Schmitt,Ignatia Van den Veyver,Christine M. Eng,Jinglan Zhang	1
3	Chromosomal microarray analysis on uncultured chorionic villus sampling can be complicated by confined placental mosaicism for aneuploidy and microdeletions 2018 ·Prenatal Diagnosis ·Shen Gu,(unknown),Ignatia B. Van den Veyver,Sandra Peacock,Janice Smith,Amy M. Breman	13
4	Positive predictive value estimates for cell-free noninvasive prenatal screening from data of a large referral genetic diagnostic laboratory 2017 ·American Journal of Obstetrics and Gynecology ·Andrea Petersen,Sau Wai Cheung,Janice Smith,Weimin Bi,Patricia A. Ward,Sandra Peacock,Alicia Braxton,Ignatia B. Van den Veyver,Amy M. Breman	127
5	Capture-based high-coverage NGS: a powerful tool to uncover a wide spectrum of mutation types 2015 ·Genetics in Medicine ·Jing Wang,(unknown),Victor Wei Zhang,Tian Xia,Yanming Feng,Guoli Wang,(unknown),Hao Wang,Richard E. Lutz,Eric Schmitt,Sandra Peacock,Lee-Jun Wong	21
6	Impact of heterozygote CFTR Mutations in COPD patients with Chronic Bronchitis 2014 ·Respiratory Research ·S. Vamsee Raju,(unknown),Sandra Peacock,Ping Fang,Robert A. Oster,Mark T. Dransfield,Steven M. Rowe	33
7	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 2011 ·American Journal of Medical Genetics Part A ·Jun Gu,Sandesh C. Sreenath Nagamani,Vicki L. Hopwood,(unknown),(unknown),Zhishuo Ou,Sandra Peacock,Dorothy K. Grange,Paweł Stankiewicz,Sau Wai Cheung	1
8	Comprehensive 5-Year Study of Cytogenetic Aberrations in 668 Infertile Men 2010 ·The Journal of Urology ·Alexander N. Yatsenko,Svetlana A. Yatsenko,John Weedin,Amy E. Lawrence,Ankita Patel,Sandra Peacock,Martin M. Matzuk,Dolores J. Lamb,Sau Wai Cheung,Larry I. Lipshultz	45
9	Complex rearrangements in patients with duplications of MECP2 can occur by fork stalling and template switching 2009 ·Human Molecular Genetics ·Claudia M.B. Carvalho,Feng Zhang,Pengfei Liu,Ankita Patel,Trilochan Sahoo,Carlos A. Bacino,Chad A. Shaw,Sandra Peacock,Amber N. Pursley,(unknown),Melissa B. Ramocki,Magdalena Nawara,Ewa Obersztyn,Angela Maria Vianna‐Morgante,Paweł Stankiewicz,Huda Y. Zoghbi,Sau Wai Cheung,James R. Lupski	146
10	Identification of critical regions for clinical features of distal 10q deletion syndrome 2009 ·Clinical Genetics ·(unknown),(unknown),(unknown),(unknown),Jane L. Schuette,(unknown),Beata Nowakowska,Sandra Peacock,(unknown),(unknown),(unknown),Zhishuo Ou,(unknown),(unknown)	48
11	Mosaicism for r(X) and der(X)del(X)(p11.23)dup(X)(p11.21p11.22) provides insight into the possible mechanism of rearrangement 2008 ·Molecular Cytogenetics ·Oleg A. Shchelochkov,M. Lance Cooper,Zhishuo Ou,Sandra Peacock,Svetlana A. Yatsenko,Chester Brown,Ping Fang,Paweł Stankiewicz,Sau Wai Cheung	11

About Sandra Peacock

Sandra Peacock is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Reproductive Medicine, having authored 11 papers that have together received 489 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Genetics and Neurodevelopmental Disorders (3 papers). The work is most often cited by research in Genetics (308 citations), Pediatrics, Perinatology and Child Health (207 citations) and Reproductive Medicine (34 citations). Sandra Peacock has collaborated with scholars based in United States and Brazil. Frequent 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. Their work appears in journals such as Human Molecular Genetics, American Journal of Obstetrics and Gynecology and The Journal of Urology.

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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