Shengru Guo

1.9k total citations · 1 hit paper
27 papers, 797 citations indexed

About

Shengru Guo is a scholar working on Molecular Biology, Genetics and Sensory Systems. According to data from OpenAlex, Shengru Guo has authored 27 papers receiving a total of 797 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Sensory Systems. Recurrent topics in Shengru Guo's work include Hearing, Cochlea, Tinnitus, Genetics (8 papers), Genetic Associations and Epidemiology (6 papers) and Genomics and Rare Diseases (4 papers). Shengru Guo is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (8 papers), Genetic Associations and Epidemiology (6 papers) and Genomics and Rare Diseases (4 papers). Shengru Guo collaborates with scholars based in United States, Türkiye and United Kingdom. Shengru Guo's co-authors include Eden R. Martin, Güney Bademci, Mustafa Tekin, Gary W. Beecham, Alan R. Sanders, Susan H. Blanton, Duygu Duman, Stephan Züchner, Karin J. H. Verweij and Abdel Abdellaoui and has published in prestigious journals such as Science, Journal of Clinical Investigation and PLoS ONE.

In The Last Decade

Shengru Guo

25 papers receiving 769 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior

2019 213 citations Andrea Ganna, Karin J. H. Verweij et al. Science profile →

Peers

Countries citing papers authored by Shengru Guo

Since Specialization

Citations

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

Fields of papers citing papers by Shengru Guo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shengru Guo

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work	Indexed citations
1	Human organoids for rapid validation of gene variants linked to cochlear malformations 2025 ·Human Genetics ·(unknown), Memoona Ramzan, Duygu Duman, (unknown), (unknown), M. Tayyar Kalcıoğlu, Suat Fítöz, (unknown), Shengru Guo, Derek M. Dykxhoorn, Mustafa Tekin	0
2	Genetic heterogeneity in hereditary hearing loss: Potential role of kinociliary protein TOGARAM2 2024 ·European Journal of Human Genetics ·Memoona Ramzan, (unknown), Clemer Abad, Shengru Guo, (unknown), Özgül M. Alper, (unknown), Tahir Atık, Duygu Duman, Güney Bademci, Barbara Vona, M. Tayyar Kalcıoğlu, Katherina Walz, Mustafa Tekin	2
3	Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss 2024 ·American Journal of Medical Genetics Part A ·Duygu Duman, Memoona Ramzan, (unknown), (unknown), (unknown), (unknown), Shengru Guo, (unknown), (unknown), M. Tayyar Kalcıoğlu, Güney Bademci, Mustafa Tekin	1
4	H4C5 missense variant leads to a neurodevelopmental phenotype overlapping with Angelman syndrome 2023 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Stephanie Bivona, (unknown), (unknown), (unknown), Shengru Guo, (unknown), (unknown), Güney Bademci, Mustafa Tekin	0
5	Genomic evidence consistent with antagonistic pleiotropy may help explain the evolutionary maintenance of same-sex sexual behaviour in humans 2021 ·Nature Human Behaviour ·Brendan P. Zietsch, Morgan J. Sidari, Abdel Abdellaoui, Robert Maier, Niklas Långström, Shengru Guo, Gary W. Beecham, Eden R. Martin, Alan R. Sanders, Karin J. H. Verweij	26
6	Genome-Wide Linkage Study Meta-Analysis of Male Sexual Orientation 2021 ·Archives of Sexual Behavior ·Alan R. Sanders, Gary W. Beecham, Shengru Guo, Judith A. Badner, Sven Bocklandt, Brian Mustanski, Dean H. Hamer, Eden R. Martin	5
7	Genome-Wide Linkage and Association Study of Childhood Gender Nonconformity in Males 2021 ·Archives of Sexual Behavior ·Alan R. Sanders, Gary W. Beecham, Shengru Guo, Khytam Dawood, Gerulf Rieger, (unknown), Alana B. Kolundzija, J. Michael Bailey, Eden R. Martin	5
8	Long-range cis-regulatory elements controlling GDF6 expression are essential for ear development 2020 ·Journal of Clinical Investigation ·Güney Bademci, Clemer Abad, Filiz Başak Cengiz, (unknown), Armağan İncesulu, Shengru Guo, Suat Fítöz, Emine İkbal Atlı, (unknown), Selma Demır, (unknown), (unknown), (unknown), Duygu Duman, Hakan Gürkan, Cynthia C. Morton, Derek M. Dykxhoorn, Katherina Walz, Mustafa Tekin	15
9	A founder noncoding GALT variant interfering with splicing causes galactosemia 2020 ·Journal of Inherited Metabolic Disease ·(unknown), (unknown), (unknown), (unknown), Shengru Guo, (unknown), Willa Thorson, Stephanie Hacker, Deborah Barbouth, Mustafa Tekin, Güney Bademci	1
10	Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior breakdown → 2019 ·Science ·Andrea Ganna, Karin J. H. Verweij, Michel G. Nivard, Robert Maier, Robbee Wedow, Alexander S. Busch, Abdel Abdellaoui, Shengru Guo, J. Fah Sathirapongsasuti, Paul Lichtenstein, Sebastian Lundström, Niklas Långström, Adam Auton, Kathleen Mullan Harris, Gary W. Beecham, Eden R. Martin, Alan R. Sanders, John R. B. Perry, Benjamin M. Neale, Brendan P. Zietsch	213
11	A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss 2019 ·Human Genetics ·(unknown), (unknown), Shengru Guo, Vladimir Camarena, Gaofeng Wang, Suna Tokgöz-Yılmaz, Duygu Duman, Güney Bademci, Mustafa Tekin	18
12	Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability 2018 ·PLoS ONE ·(unknown), Katherine E. Masih, Nursel Elçioğlu, (unknown), (unknown), Filiz Başak Cengiz, (unknown), (unknown), (unknown), (unknown), Shengru Guo, Duygu Duman, Güney Bademci, Mustafa Tekin	18
13	Novel EYA1 variants causing Branchio-oto-renal syndrome 2017 ·International Journal of Pediatric Otorhinolaryngology ·(unknown), (unknown), Selçuk Arslan, (unknown), Hakan Gürkan, Selma Demır, Reza Maroofian, (unknown), (unknown), (unknown), Nursel Elçioğlu, Ibis Menéndez, Mahdiyeh Behnam, Joseph Foster, Shengru Guo, (unknown), Filiz Başak Cengiz, Duygu Duman, Güney Bademci, Mustafa Tekin	15
14	Evaluating genetic susceptibility to Staphylococcus aureus bacteremia in African Americans using admixture mapping 2017 ·Genes and Immunity ·Derek D. Cyr, Andrew S. Allen, (unknown), Felicia Ruffin, (unknown), Joshua T. Thaden, Stacey A. Maskarinec, Maria Souli, Shengru Guo, Derek M. Dykxhoorn, William K. Scott, Vance G. Fowler	23
15	A next-generation sequencing gene panel (MiamiOtoGenes) for comprehensive analysis of deafness genes 2016 ·Hearing Research ·Demet Tekin, Denise Yan, Güney Bademci, Yong Feng, Shengru Guo, Joseph Foster, Susan H. Blanton, Mustafa Tekin, Xuezhong Liu	34
16	Rare Variants in NOD1 Associated with Carotid Bifurcation Intima-Media Thickness in Dominican Republic Families 2016 ·PLoS ONE ·Nicole Dueker, Ashley Beecham, Liyong Wang, Susan H. Blanton, Shengru Guo, Tatjana Rundek, Ralph L. Sacco	4
17	Identification of Copy Number Variants Through Whole-Exome Sequencing in Autosomal Recessive Nonsyndromic Hearing Loss 2014 ·Genetic Testing and Molecular Biomarkers ·Güney Bademci, Oscar Diaz‐Horta, Shengru Guo, Duygu Duman, Derek Van Booven, Joseph Foster, Filiz Başak Cengiz, Susan H. Blanton, Mustafa Tekin	26
18	Genome-wide scan demonstrates significant linkage for male sexual orientation 2014 ·Psychological Medicine ·Alan R. Sanders, Eden R. Martin, Gary W. Beecham, Shengru Guo, Khytam Dawood, Gerulf Rieger, Judith A. Badner, Elliot S. Gershon, (unknown), Alana B. Kolundzija, Jubao Duan, Pablo V. Gejman, J. Michael Bailey	84
19	Linkage and association of successful aging to the 6q25 region in large Amish kindreds 2012 ·AGE ·Digna R. Velez Edwards, John R. Gilbert, James E. Hicks, Jamie L. Myers, Lan Jiang, Anna Cummings, Shengru Guo, Paul J. Gallins, Ioanna Konidari, (unknown), (unknown), (unknown), (unknown), Reneé A. Laux, Charles E. Jackson, Margaret A. Pericak‐Vance, Jonathan L. Haines, William K. Scott	14
20	Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia 2011 ·The American Journal of Human Genetics ·Aslı Sırmacı, Michail Spiliopoulos, Francesco Brancati, Eric Powell, Duygu Duman, (unknown), Güney Bademci, Emanuele Agolini, Shengru Guo, (unknown), Aslı Kavaz, Susan H. Blanton, M. Cristina Digilio, Bruno Dallapiccola, Juan I. Young, Stephan Züchner, Mustafa Tekin	170

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.

Explore authors with similar magnitude of impact