Cuiping Hou

11.2k total citations
39 papers, 1.6k citations indexed

About

Cuiping Hou is a scholar working on Genetics, Molecular Biology and Neurology. According to data from OpenAlex, Cuiping Hou has authored 39 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 22 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in Cuiping Hou's work include Genomic variations and chromosomal abnormalities (9 papers), Genetic Associations and Epidemiology (8 papers) and Genomics and Rare Diseases (5 papers). Cuiping Hou is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Genetic Associations and Epidemiology (8 papers) and Genomics and Rare Diseases (5 papers). Cuiping Hou collaborates with scholars based in United States, United Kingdom and Australia. Cuiping Hou's co-authors include Håkon Håkonarson, Joseph Glessner, Kai Wang, Sharon J. Diskin, John M. Maris, Mingyao Li, Cecilia Kim, Rosetta Chiavacci, Jonathan P. Bradfield and Shuzhang Yang and has published in prestigious journals such as Nucleic Acids Research, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Cuiping Hou

38 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Cuiping Hou United States 20 791 740 292 253 236 39 1.6k
Philipp Rentzsch Germany 3 1.1k 1.4× 1.3k 1.7× 234 0.8× 134 0.5× 107 0.5× 6 2.2k
J D Gearhart United States 25 586 0.7× 1.1k 1.6× 190 0.7× 160 0.6× 96 0.4× 35 2.0k
Ann Nordgren Sweden 29 997 1.3× 1.1k 1.5× 246 0.8× 144 0.6× 58 0.2× 134 2.6k
Pei‐Lung Chen Taiwan 21 287 0.4× 530 0.7× 119 0.4× 130 0.5× 145 0.6× 102 1.4k
Tommaso Pippucci Italy 23 663 0.8× 708 1.0× 215 0.7× 53 0.2× 99 0.4× 71 1.5k
Stefan Schmidt Austria 18 255 0.3× 718 1.0× 223 0.8× 260 1.0× 59 0.3× 40 1.4k
Sophie Nicole France 25 391 0.5× 1.4k 1.8× 83 0.3× 111 0.4× 267 1.1× 60 2.2k
Dorota Monies Saudi Arabia 22 507 0.6× 579 0.8× 73 0.3× 188 0.7× 69 0.3× 48 1.3k
Ana Cristina Victorino Krepischi Brazil 27 1.4k 1.8× 1.4k 1.9× 438 1.5× 100 0.4× 64 0.3× 146 2.7k
Toshiki Takenouchi Japan 20 525 0.7× 689 0.9× 63 0.2× 106 0.4× 139 0.6× 141 1.6k

Countries citing papers authored by Cuiping Hou

Since Specialization
Citations

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

Fields of papers citing papers by Cuiping Hou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cuiping Hou

This figure shows the co-authorship network connecting the top 25 collaborators of Cuiping Hou. A scholar is included among the top collaborators of Cuiping Hou 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 Cuiping Hou. Cuiping Hou 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.
Qu, Hui‐Qi, Charlly Kao, James Garifallou, et al.. (2023). Single Cell Transcriptome Analysis of Peripheral Blood Mononuclear Cells in Freshly Isolated versus Stored Blood Samples. Genes. 14(1). 142–142. 3 indexed citations
2.
Li, Dong, Alanna Strong, Cuiping Hou, et al.. (2022). Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphism. Molecular Cytogenetics. 15(1). 33–33. 1 indexed citations
3.
Strong, Alanna, Gina O’Grady, Jonathan Bishop, et al.. (2021). A new syndrome of moyamoya disease, kidney dysplasia, aminotransferase elevation, and skin disease associated with de novo variants in RNF213. American Journal of Medical Genetics Part A. 185(7). 2168–2174. 11 indexed citations
4.
Strong, Alanna, Michael March, Christopher J. Cardinale, et al.. (2021). A novel MBTPS2 variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response. American Journal of Medical Genetics Part A. 188(2). 463–472. 4 indexed citations
5.
Chang, Xiao, Hui‐Qi Qu, Yichuan Liu, et al.. (2019). Microduplications at the 15q11.2 BP1–BP2 locus are enriched in patients with anorexia nervosa. Journal of Psychiatric Research. 113. 34–38. 9 indexed citations
6.
McDaniel, Lee, Karina L. Conkrite, Xiao Chang, et al.. (2017). Common variants upstream of MLF1 at 3q25 and within CPZ at 4p16 associated with neuroblastoma. PLoS Genetics. 13(5). e1006787–e1006787. 63 indexed citations
7.
Chang, Xiao, Dong Li, Lifeng Tian, et al.. (2017). Heterozygous Deletion Impacting SMARCAD1 in the Original Kindred with Absent Dermatoglyphs and Associated Features (Baird, 1964). The Journal of Pediatrics. 194. 248–252.e2. 3 indexed citations
8.
Keller, Michael D., Rahul Pandey, Dong Li, et al.. (2016). Mutation in IRF2BP2 is responsible for a familial form of common variable immunodeficiency disorder. Journal of Allergy and Clinical Immunology. 138(2). 544–550.e4. 53 indexed citations
9.
Cardinale, Christopher J., Dong Li, Lifeng Tian, et al.. (2016). Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study. BMC Musculoskeletal Disorders. 17(1). 462–462. 11 indexed citations
10.
Chang, Xiao, Joseph Glessner, Adrienne Tin, et al.. (2015). Genome-wide association study reveals two loci for serum magnesium concentrations in European-American children. Scientific Reports. 5(1). 18792–18792. 2 indexed citations
11.
Maggadóttir, Sólrún Melkorka, Jin Li, Joseph Glessner, et al.. (2015). Rare variants at 16p11.2 are associated with common variable immunodeficiency. Journal of Allergy and Clinical Immunology. 135(6). 1569–1577. 19 indexed citations
12.
Shi, Lingling, Xu Zhang, Ryan Golhar, et al.. (2013). Whole-genome sequencing in an autism multiplex family. Molecular Autism. 4(1). 8–8. 54 indexed citations
13.
Li, Jin, Joseph Glessner, Haitao Zhang, et al.. (2012). GWAS of blood cell traits identifies novel associated loci and epistatic interactions in Caucasian and African-American children. Human Molecular Genetics. 22(7). 1457–1464. 58 indexed citations
14.
Orange, Jordan S., Joseph Glessner, Elena S. Resnick, et al.. (2011). Genome-wide association identifies diverse causes of common variable immunodeficiency. Journal of Allergy and Clinical Immunology. 127(6). 1360–1367.e6. 138 indexed citations
15.
Zhao, Jianhua, Mingyao Li, Jonathan P. Bradfield, et al.. (2010). The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature. BMC Medical Genetics. 11(1). 96–96. 46 indexed citations
16.
Attiyeh, Edward F., Sharon J. Diskin, Marc A. Attiyeh, et al.. (2009). Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy. Genome Research. 19(2). 276–283. 66 indexed citations
17.
Duan, Jubao, María Martínez, Alan R. Sanders, et al.. (2007). <i>DTNBP1 (Dystrobrevin Binding Protein 1)</i> and Schizophrenia: Association Evidence in the 3′ End of the Gene. Human Heredity. 64(2). 97–106. 32 indexed citations
18.
Duan, Jubao, María Martínez, Alan R. Sanders, et al.. (2004). Polymorphisms in the Trace Amine Receptor 4 (TRAR4) Gene on Chromosome 6q23.2 Are Associated with Susceptibility to Schizophrenia. The American Journal of Human Genetics. 75(4). 624–638. 66 indexed citations
19.
Duan, Jubao, Cuiping Hou, Naruya Saitou, et al.. (2004). Polymorphisms in trace amine receptor 4 (TRAR4) are associated with susceptibility for schizophrenia on chromosome 6q23.2. American Journal of Medical Genetics Part A. 19–20. 2 indexed citations
20.
Sanders, Alan R., Jubao Duan, Cuiping Hou, et al.. (2004). Haplotypic association spanning the 22q11.21 genes COMT and ARVCF with schizophrenia. Molecular Psychiatry. 10(4). 353–365. 62 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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