Patricia Hixson

1.7k total citations
22 papers, 839 citations indexed

About

Patricia Hixson is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Patricia Hixson has authored 22 papers receiving a total of 839 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 11 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Patricia Hixson's work include Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (6 papers) and Genomics and Rare Diseases (5 papers). Patricia Hixson is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Prenatal Screening and Diagnostics (6 papers) and Genomics and Rare Diseases (5 papers). Patricia Hixson collaborates with scholars based in United States, Poland and Canada. Patricia Hixson's co-authors include Ankita Patel, Paweł Stankiewicz, Chad A. Shaw, Sau Wai Cheung, James R. Lupski, Hanwen Zhu, Ji Sun, Weimin Bi, Seema R. Lalani and Carlos A. Bacino and has published in prestigious journals such as Cell, Nucleic Acids Research and Blood.

In The Last Decade

Patricia Hixson

22 papers receiving 829 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patricia Hixson United States 16 537 413 202 146 93 22 839
Fabienne Giuliano France 17 549 1.0× 698 1.7× 80 0.4× 33 0.2× 30 0.3× 38 1.1k
Cécile Mignon‐Ravix France 15 320 0.6× 475 1.2× 90 0.4× 72 0.5× 10 0.1× 26 727
Penny Clouston United Kingdom 12 452 0.8× 613 1.5× 58 0.3× 71 0.5× 14 0.2× 34 850
Sabine Endele Germany 14 309 0.6× 701 1.7× 52 0.3× 57 0.4× 14 0.2× 22 908
Marina Murdolo Italy 13 491 0.9× 383 0.9× 146 0.7× 171 1.2× 7 0.1× 20 663
Daniela Balzereit Germany 6 180 0.3× 663 1.6× 39 0.2× 40 0.3× 109 1.2× 6 898
Lara Moumné France 11 251 0.5× 386 0.9× 21 0.1× 71 0.5× 33 0.4× 11 629
Tahsin Stefan Barakat Netherlands 18 722 1.3× 1.3k 3.1× 32 0.2× 112 0.8× 17 0.2× 45 1.5k
Shirley He United States 11 376 0.7× 995 2.4× 36 0.2× 70 0.5× 45 0.5× 14 1.3k
Sung-Hae L. Kang United States 8 312 0.6× 474 1.1× 109 0.5× 49 0.3× 5 0.1× 8 756

Countries citing papers authored by Patricia Hixson

Since Specialization
Citations

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

Fields of papers citing papers by Patricia Hixson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patricia Hixson

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

All Works

20 of 20 papers shown
1.
Zhu, Hanwen, Patricia Hixson, Wen Ma, & Ji Sun. (2024). Pharmacology of LRRK2 with type I and II kinase inhibitors revealed by cryo-EM. Cell Discovery. 10(1). 10–10. 25 indexed citations
2.
Palicharla, Vivek Reddy, Darcie J. Miller, Sun‐Hee Hwang, et al.. (2023). Human IFT-A complex structures provide molecular insights into ciliary transport. Cell Research. 33(4). 288–298. 26 indexed citations
3.
Myasnikov, Alexander, Hanwen Zhu, Patricia Hixson, et al.. (2021). Structural analysis of the full-length human LRRK2. Cell. 184(13). 3519–3527.e10. 112 indexed citations
4.
Startek, Michał, Przemysław Szafrański, Tomasz Gambin, et al.. (2015). Genome-wide analyses of LINE–LINE-mediated nonallelic homologous recombination. Nucleic Acids Research. 43(4). 2188–2198. 61 indexed citations
5.
Shaw, Chad A., Amber N. Pursley, Patricia Hixson, et al.. (2014). Somatic mosaicism detected by exon-targeted, high-resolution aCGH in 10 362 consecutive cases. European Journal of Human Genetics. 22(8). 969–978. 35 indexed citations
6.
Campbell, Ian M., Tomasz Gambin, Piotr Dittwald, et al.. (2014). Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination. BMC Biology. 12(1). 74–74. 51 indexed citations
7.
Szafrański, Przemysław, Sailaja Golla, Weihong Jin, et al.. (2014). Neurodevelopmental and neurobehavioral characteristics in males and females with CDKL5 duplications. European Journal of Human Genetics. 23(7). 915–921. 32 indexed citations
8.
Chanprasert, Sirisak, Janice Smith, Patricia Hixson, Ankita Patel, & Seema R. Lalani. (2014). Heterozygous deletion of exons 18 and 19 of IGF1R in an individual with short stature. Clinical Dysmorphology. 23(3). 98–100. 1 indexed citations
9.
Wiszniewska, Joanna, Weimin Bi, Chad A. Shaw, et al.. (2013). Combined array CGH plus SNP genome analyses in a single assay for optimized clinical testing. European Journal of Human Genetics. 22(1). 79–87. 77 indexed citations
10.
Witsch, Jens, Przemysław Szafrański, Chun‐An Chen, et al.. (2013). Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delay. European Journal of Human Genetics. 21(11). 1304–1307. 10 indexed citations
11.
Burrage, Lindsay C., Tanya N. Eble, Patricia Hixson, et al.. (2013). A mosaic 2q24.2 deletion narrows the critical region to a 0.4 Mb interval that includes TBR1, TANK, and PSMD14. American Journal of Medical Genetics Part A. 161(4). 841–844. 15 indexed citations
12.
Boone, Philip M., Ian M. Campbell, Zachry T. Soens, et al.. (2013). Deletions of recessive disease genes: CNV contribution to carrier states and disease-causing alleles. Genome Research. 23(9). 1383–1394. 45 indexed citations
13.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Frank J. Probst, et al.. (2012). Small genomic rearrangements involving FMR1 support the importance of its gene dosage for normal neurocognitive function. Neurogenetics. 13(4). 333–339. 20 indexed citations
14.
Bi, Weimin, Amber N. Pursley, Patricia Hixson, et al.. (2012). Comparison of chromosome analysis and chromosomal microarray analysis: what is the value of chromosome analysis in today’s genomic array era?. Genetics in Medicine. 15(6). 450–457. 52 indexed citations
15.
Yatsenko, Svetlana A., Patricia Hixson, Erin K. Roney, et al.. (2012). Human subtelomeric copy number gains suggest a DNA replication mechanism for formation: beyond breakage–fusion–bridge for telomere stabilization. Human Genetics. 131(12). 1895–1910. 31 indexed citations
16.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Carolyn Bay, et al.. (2011). Delineation of a deletion region critical for corpus callosal abnormalities in chromosome 1q43–q44. European Journal of Human Genetics. 20(2). 176–179. 38 indexed citations
17.
Shao, Lina, Sung-Hae L. Kang, Jian Li, et al.. (2010). Array Comparative Genomic Hybridization Detects Chromosomal Abnormalities in Hematological Cancers That Are Not Detected by Conventional Cytogenetics. Journal of Molecular Diagnostics. 12(5). 670–679. 18 indexed citations
18.
Nagamani, Sandesh C. Sreenath, Ayelet Erez, Patricia I. Bader, et al.. (2010). Phenotypic manifestations of copy number variation in chromosome 16p13.11. European Journal of Human Genetics. 19(3). 280–286. 83 indexed citations
19.
Xiong, Changyun, Patricia Hixson, Leonardo H. Mendoza, & C. Wayne Smith. (2005). Cloning and expression of rabbit interleukin-15. Veterinary Immunology and Immunopathology. 107(1-2). 131–141. 7 indexed citations
20.
Hixson, Patricia, C. Wayne Smith, Susan B. Shurin, & Michael F. Tosi. (2003). Unique CD18 mutations involving a deletion in the extracellular stalk region and a major truncation of the cytoplasmic domain in a patient with leukocyte adhesion deficiency type 1. Blood. 103(3). 1105–1113. 10 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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