Patrick Sleiman

18.5k total citations
94 papers, 2.4k citations indexed

About

Patrick Sleiman is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Patrick Sleiman has authored 94 papers receiving a total of 2.4k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Genetics, 32 papers in Molecular Biology and 17 papers in Surgery. Recurrent topics in Patrick Sleiman's work include Genetic Associations and Epidemiology (20 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Patrick Sleiman is often cited by papers focused on Genetic Associations and Epidemiology (20 papers), Genomic variations and chromosomal abnormalities (13 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Patrick Sleiman collaborates with scholars based in United States, China and United Kingdom. Patrick Sleiman's co-authors include Håkon Håkonarson, Struan F.A. Grant, Joseph Glessner, Frank Mentch, Rosetta Chiavacci, Haijun Qiu, Raquel E. Gur, Xiao Chang, Jonathan P. Bradfield and Hui‐Qi Qu and has published in prestigious journals such as Nature Communications, Immunity and The Journal of Immunology.

In The Last Decade

Patrick Sleiman

93 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Patrick Sleiman United States	24	768	632	448	366	332	94	2.4k
Brendan J. Keating United States	28	823 1.1×	909 1.4×	401 0.9×	279 0.8×	252 0.8×	102	2.8k
Kristleifur Kristjánsson Iceland	29	744 1.0×	722 1.1×	208 0.5×	294 0.8×	233 0.7×	46	2.7k
Jennifer M. Kwon United States	29	634 0.8×	1.2k 1.9×	302 0.7×	718 2.0×	110 0.3×	77	3.4k
Joseph M. Devaney United States	31	1.3k 1.7×	1.4k 2.2×	281 0.6×	536 1.5×	167 0.5×	95	3.5k
Thomas F. Wienker Germany	32	755 1.0×	1.9k 3.0×	642 1.4×	317 0.9×	462 1.4×	79	4.1k
Derek Gordon United States	32	1.5k 1.9×	1.3k 2.0×	401 0.9×	233 0.6×	340 1.0×	129	3.5k
Jacob L. McCauley United States	26	954 1.2×	834 1.3×	158 0.4×	162 0.4×	780 2.3×	74	3.0k
Verneri Anttila United States	18	1.9k 2.4×	764 1.2×	178 0.4×	361 1.0×	125 0.4×	30	3.2k
Jangsup Moon South Korea	32	386 0.5×	739 1.2×	316 0.7×	208 0.6×	164 0.5×	166	3.4k
Joyce Y. Tung United States	20	1.2k 1.6×	840 1.3×	151 0.3×	386 1.1×	167 0.5×	28	3.1k

Countries citing papers authored by Patrick Sleiman

Since Specialization

Citations

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

Fields of papers citing papers by Patrick Sleiman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick Sleiman

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

All Works

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20 of 20 papers shown

Qu, Hui‐Qi, John J. Connolly, Peter Kraft, et al.. (2023). Trans‐ethnic polygenic risk scores for body mass index: An international hundred K+ cohorts consortium study. Clinical and Translational Medicine. 13(6). e1291–e1291. 3 indexed citations

Singhal, Pankhuri, Yogasudha Veturi, Scott Dudek, et al.. (2023). Evidence of epistasis in regions of long-range linkage disequilibrium across five complex diseases in the UK Biobank and eMERGE datasets. The American Journal of Human Genetics. 110(4). 575–591. 9 indexed citations

Glessner, Joseph, Xiao Chang, Yichuan Liu, et al.. (2023). Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders. Journal of Neurodevelopmental Disorders. 15(1). 14–14. 5 indexed citations

Qu, Hui‐Qi, James W. Snyder, Joseph Glessner, et al.. (2022). Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ Injuries. Biomedicines. 10(2). 264–264. 11 indexed citations

Liu, Yichuan, Hui‐Qi Qu, Xiao Chang, et al.. (2022). Mutation burden analysis of six common mental disorders in African Americans by whole genome sequencing. Human Molecular Genetics. 31(22). 3769–3776. 6 indexed citations

Qu, Hui‐Qi, Joseph Glessner, Frank Mentch, et al.. (2022). Metabolomic profiling of samples from pediatric patients with asthma unveils deficient nutrients in African Americans. iScience. 25(7). 104650–104650. 8 indexed citations

Glessner, Joseph, Jin Li, Yichuan Liu, et al.. (2022). ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studies. European Journal of Human Genetics. 31(3). 304–312. 3 indexed citations

Liu, Yichuan, Hui‐Qi Qu, Xiao Chang, et al.. (2021). Deep learning prediction of attention-deficit hyperactivity disorder in African Americans by copy number variation. Experimental Biology and Medicine. 246(21). 2317–2323. 13 indexed citations

Chang, Xiao, Yun Li, Kenny Nguyen, et al.. (2021). Genetic correlations between COVID-19 and a variety of traits and diseases. The Innovation. 2(2). 100112–100112. 5 indexed citations

10.

Liu, Yichuan, Hui‐Qi Qu, Xiao Chang, et al.. (2021). Machine Learning Reduced Gene/Non-Coding RNA Features That Classify Schizophrenia Patients Accurately and Highlight Insightful Gene Clusters. International Journal of Molecular Sciences. 22(7). 3364–3364. 7 indexed citations

11.

Al‐Harbi, Talal, et al.. (2021). Rare neurological manifestations in a Saudi Arabian patient with Ehlers–Danlos syndrome and a novel homozygous variant in the TNXB gene. American Journal of Medical Genetics Part A. 188(2). 618–623. 2 indexed citations

12.

Liu, Yichuan, Hui‐Qi Qu, Xiao Chang, et al.. (2020). Interpretation of Maturity-Onset Diabetes of the Young Genetic Variants Based on American College of Medical Genetics and Genomics Criteria: Machine-Learning Model Development. 5(1). e20506–e20506. 1 indexed citations

13.

Almoguera, Berta, Lyam Vazquez, Frank Mentch, et al.. (2018). Novel locus for atopic dermatitis in African Americans and replication in European Americans. Journal of Allergy and Clinical Immunology. 143(3). 1229–1231. 8 indexed citations

14.

Zhang, Yu, Lifeng Tian, Patrick Sleiman, Soumitra Ghosh, & Håkon Håkonarson. (2017). Bayesian analysis of genome-wide inflammatory bowel disease data sets reveals new risk loci. European Journal of Human Genetics. 26(2). 265–274. 14 indexed citations

15.

Almoguera, Berta, Lyam Vazquez, John J. Connolly, et al.. (2014). Imputation of TPMT defective alleles for the identification of patients with high-risk phenotypes. Frontiers in Genetics. 5. 96–96. 12 indexed citations

16.

Sleiman, Patrick, Jonathan P. Bradfield, Frank Mentch, et al.. (2014). Assessing the functional consequence of loss of function variants using electronic medical record and large-scale genomics consortium efforts. Frontiers in Genetics. 5. 105–105. 3 indexed citations

17.

Li, Jin, Joseph M. McDonough, Zhi Wei, et al.. (2013). Gene Network Analysis in a Pediatric Cohort Identifies Novel Lung Function Genes. PLoS ONE. 8(9). e72899–e72899. 17 indexed citations

18.

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

19.

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

20.

Bisgaard, Hans, Klaus Bønnelykke, Patrick Sleiman, et al.. (2008). Chromosome 17q21 Gene Variants Are Associated with Asthma and Exacerbations but Not Atopy in Early Childhood. American Journal of Respiratory and Critical Care Medicine. 179(3). 179–185. 158 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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