Patricia A. Eng

899 citations

5 papers · 298 indexed · h-index 5

Genetics top 10%
Molecular Biology
Pediatrics, Perinatology and Child Health top 10%
Plant Science
Cognitive Neuroscience

Co-authors: Sau Wai Cheung Ankita Patel Paweł Stankiewicz Trilochan Sahoo Chad A. Shaw Zhishuo Ou A. Craig Chinault M. Lance Cooper
Topics: Genomic variations and chromosomal abnormalities (4 papers)Congenital heart defects research (3 papers)Genetics and Neurodevelopmental Disorders (2 papers)
Cited by: Genetics Pediatrics, Perinatology and Child Health Molecular Biology
Journals: European Journal of Human Genetics Prenatal Diagnosis American Journal of Medical Genetics Part A
Partner nations: United States Canada

In The Last Decade

Patricia A. Eng

5 papers receiving 283 citations

Peers

Countries citing papers authored by Patricia A. Eng

Since Specialization

Citations

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

Fields of papers citing papers by Patricia A. Eng

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Patricia A. Eng. 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 Patricia A. Eng. The network helps show where Patricia A. Eng may publish in the future.

Co-authorship network of co-authors of Patricia A. Eng

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

All Works

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5 of 5 papers shown

#	Work	Indexed citations
1	Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders 2012 ·Molecular Cytogenetics ·Patrícia B. S. Celestino-Soper,Cindy Skinner,Richard J. Schroer,Patricia A. Eng,(unknown),(unknown),Deborah Terespolsky,(unknown),Gayle Patel,LaDonna Immken,Alecia Willis,Joanna Wiszniewska,Reuben Matalon,Jill A. Rosenfeld,Roger E. Stevenson,Sung-Hae L. Kang,Sau Wai Cheung,Arthur L. Beaudet,Paweł Stankiewicz	41
2	Phenotypic manifestations of copy number variation in chromosome 16p13.11 2010 ·European Journal of Human Genetics ·Sandesh C. Sreenath Nagamani,Ayelet Erez,Patricia I. Bader,Seema R. Lalani,Daryl A. Scott,Fernando Scaglia,Sharon E. Plon,(unknown),Tyler Reimschisel,Elizabeth Roeder,(unknown),Patricia A. Eng,Patricia Hixson,Sung-Hae L. Kang,Paweł Stankiewicz,Ankita Patel,Sau Wai Cheung	83
3	Insertional translocation detected using FISH confirmation of array‐comparative genomic hybridization (aCGH) results 2010 ·American Journal of Medical Genetics Part A ·Sung‐Hae Kang,Chad A. Shaw,Zhishuo Ou,Patricia A. Eng,M. Lance Cooper,Amber N. Pursley,Trilochan Sahoo,Carlos A. Bacino,A. Craig Chinault,Paweł Stankiewicz,Ankita Patel,James R. Lupski,Sau Wai Cheung	79
4	Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH 2008 ·Prenatal Diagnosis ·Weimin Bi,Amy M. Breman,Susan Venable,Patricia A. Eng,Trilochan Sahoo,(unknown),Ankita Patel,Arthur L. Beaudet,Sau Wai Cheung,Lisa D. White	51
5	Chromosomal microarray analysis (CMA) detects a large X chromosome deletion including FMR1, FMR2, and IDS in a female patient with mental retardation 2007 ·American Journal of Medical Genetics Part A ·Frank J. Probst,Elizabeth Roeder,(unknown),Zhishuo Ou,M. Lance Cooper,Patricia A. Eng,Jiangzhen Li,Yanghong Gu,Robert F. Stratton,A. Craig Chinault,Chad A. Shaw,V. Reid Sutton,Sau Wai Cheung,David L. Nelson	44

About Patricia A. Eng

Patricia A. Eng is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Plant Science, having authored 5 papers that have together received 298 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), Congenital heart defects research (3 papers) and Genetics and Neurodevelopmental Disorders (2 papers). The work is most often cited by research in Genetics (243 citations), Pediatrics, Perinatology and Child Health (104 citations) and Molecular Biology (134 citations). Patricia A. Eng has collaborated with scholars based in United States and Canada. Frequent co-authors include Sau Wai Cheung, Ankita Patel, Paweł Stankiewicz, Trilochan Sahoo, Chad A. Shaw, Zhishuo Ou, A. Craig Chinault, M. Lance Cooper, Elizabeth Roeder and Sung-Hae L. Kang. Their work appears in journals such as European Journal of Human Genetics, Prenatal Diagnosis and American Journal of Medical Genetics Part A.

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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