Patrick A. Lundquist

733 total citations
16 papers, 440 citations indexed

About

Patrick A. Lundquist is a scholar working on Genetics, Molecular Biology and Hematology. According to data from OpenAlex, Patrick A. Lundquist has authored 16 papers receiving a total of 440 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Hematology. Recurrent topics in Patrick A. Lundquist's work include Iron Metabolism and Disorders (4 papers), Hemoglobinopathies and Related Disorders (4 papers) and Prenatal Screening and Diagnostics (3 papers). Patrick A. Lundquist is often cited by papers focused on Iron Metabolism and Disorders (4 papers), Hemoglobinopathies and Related Disorders (4 papers) and Prenatal Screening and Diagnostics (3 papers). Patrick A. Lundquist collaborates with scholars based in United States and China. Patrick A. Lundquist's co-authors include Karen Snow, John F. O’Brien, Walter D. Park, Daniel Kraft, Marc C. Patterson, D. Brian Dawson, Pamela S. Karnes, Cate Walsh Vockley, Vishwajeet Puri and Richard E. Pagano and has published in prestigious journals such as Blood, Neurology and Journal of the American Society of Nephrology.

In The Last Decade

Patrick A. Lundquist

16 papers receiving 429 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Patrick A. Lundquist United States 8 238 130 105 55 51 16 440
Alexander Broomfield United Kingdom 14 358 1.5× 205 1.6× 81 0.8× 63 1.1× 40 0.8× 54 613
Julie Simon United States 8 234 1.0× 82 0.6× 66 0.6× 39 0.7× 72 1.4× 8 429
Hadhami Ben Turkia Tunisia 13 417 1.8× 171 1.3× 151 1.4× 39 0.7× 31 0.6× 46 524
Hana Vlášková Czechia 13 272 1.1× 179 1.4× 55 0.5× 40 0.7× 27 0.5× 27 483
Joyce A. Kobori United States 11 329 1.4× 277 2.1× 80 0.8× 93 1.7× 21 0.4× 14 686
Norberto Guelbert Argentina 16 514 2.2× 148 1.1× 68 0.6× 58 1.1× 27 0.5× 39 651
Miriam Rigoldi Italy 16 286 1.2× 119 0.9× 88 0.8× 83 1.5× 15 0.3× 29 544
An Dang United States 12 191 0.8× 189 1.5× 32 0.3× 57 1.0× 31 0.6× 37 468
F. A. Beemer Netherlands 12 293 1.2× 232 1.8× 92 0.9× 167 3.0× 17 0.3× 21 714
Tracey Sikora United States 11 396 1.7× 202 1.6× 76 0.7× 189 3.4× 77 1.5× 15 677

Countries citing papers authored by Patrick A. Lundquist

Since Specialization
Citations

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

Fields of papers citing papers by Patrick A. Lundquist

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Patrick A. Lundquist

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

All Works

16 of 16 papers shown
1.
Lundquist, Patrick A., Lisa A. Schimmenti, Nadir Demirel, et al.. (2022). Aminoglycoside induced ototoxicity risk in the cystic fibrosis population: The utility of large‐scale screening. Pediatric Pulmonology. 58(3). 819–824. 4 indexed citations
2.
Jenkinson, Garrett, Ross A. Aleff, Christopher A. Hilker, et al.. (2021). Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing. Journal of Molecular Diagnostics. 23(12). 1732–1740. 10 indexed citations
3.
Butz, Malinda L., Patrick A. Lundquist, Mélanie Meyer, et al.. (2020). Development and Validation of a Next-Generation Sequencing Panel for Syndromic and Nonsyndromic Hearing Loss. The Journal of Applied Laboratory Medicine. 5(3). 467–479. 4 indexed citations
4.
Ida, Cristiane M., Malinda L. Butz, Patrick A. Lundquist, & D. Brian Dawson. (2018). C9orf72 Repeat Expansion Frequency among Patients with Huntington Disease Genetic Testing. Neurodegenerative Diseases. 18(5-6). 239–253. 7 indexed citations
5.
Faqeih, Eissa, et al.. (2017). A novel deletion of SNURF/SNRPN exon 1 in a patient with Prader-Willi-like phenotype. European Journal of Medical Genetics. 60(8). 416–420. 14 indexed citations
6.
Wang, Wei, Chen Wang, D. Brian Dawson, et al.. (2016). Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy. Neurology. 86(19). 1762–1771. 42 indexed citations
7.
Lundquist, Patrick A., et al.. (2015). Deletional HPFH Vs. Delta Beta Thalassemia: Closing in on a Possible Hb F Silencer Location. Blood. 126(23). 3372–3372. 3 indexed citations
8.
Oliveira, Jennifer L., et al.. (2015). Large Deletions Involving the Beta Globin Gene Complex: Genotype-Phenotype Correlation of 119 Cases. Blood. 126(23). 3374–3374. 1 indexed citations
9.
Aypar, Umut, et al.. (2014). Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader–Willi/Angelman syndrome critical region. American Journal of Medical Genetics Part A. 164(10). 2514–2520. 7 indexed citations
10.
11.
Milosevic, Dragana, Patrick A. Lundquist, Kendall W Cradic, et al.. (2010). Development and validation of a comprehensive mutation and deletion detection assay for SDHB, SDHC, and SDHD. Clinical Biochemistry. 43(7-8). 700–704. 3 indexed citations
12.
Monico, Carla G., Sandro Rossetti, Julie B. Olson, et al.. (2007). Comprehensive Mutation Screening in 55 Probands with Type 1 Primary Hyperoxaluria Shows Feasibility of a Gene-Based Diagnosis. Journal of the American Society of Nephrology. 18(6). 1905–1914. 53 indexed citations
13.
Park, Walter D., John F. O’Brien, Patrick A. Lundquist, et al.. (2003). Identification of 58 novel mutations in Niemann-Pick disease type C: Correlation with biochemical phenotype and importance ofPTC1-like domains inNPC1. Human Mutation. 22(4). 313–325. 146 indexed citations
14.
Sun, Xiaofeng, David L. Marks, Walter D. Park, et al.. (2001). Niemann-Pick C Variant Detection by Altered Sphingolipid Trafficking and Correlation with Mutations within a Specific Domain of NPC1. The American Journal of Human Genetics. 68(6). 1361–1372. 115 indexed citations
15.
Snow, Karen, Patrick A. Lundquist, Cate Walsh Vockley, et al.. (2000). Genetic testing for Niemann-Pick Type C disease. Genetics in Medicine. 2(1). 107–107. 1 indexed citations
16.
Olson, Timothy M., Steven Thibodeau, Patrick A. Lundquist, Daniel J. Schaid, & Virginia V. Michels. (1995). Exclusion of a primary gene defect at the HLA locus in familial idiopathic dilated cardiomyopathy.. Journal of Medical Genetics. 32(11). 876–880. 5 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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