Patrick A. Lundquist

733 citations

16 papers · 440 indexed · h-index 8

Impact in

Physiology top 10%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
Hematology

Papers in ⓘ

Genetics 5
- Hemoglobinopathies and Related Disorders 4
- Genetic Syndromes and Imprinting 2
Molecular Biology 4
- Epigenetics and DNA Methylation 2

Co-authors: Daniel Kraft (2 shared papers)Karen Snow (3 shared papers)Walter D. Park (2 shared papers)Marc C. Patterson (3 shared papers)John F. O’Brien (3 shared papers)D. Brian Dawson (5 shared papers)Pamela S. Karnes (2 shared papers)Cate Walsh Vockley (2 shared papers)
Journals: Journal of Molecular Diagnostics (2 papers)Blood (2 papers)Neurodegenerative Diseases (1 paper)Human Mutation (1 paper)Journal of the American Society of Nephrology (1 paper)
Partner nations: United States China

In The Last Decade

Patrick A. Lundquist

16 papers receiving 429 citations

Peers

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-authors

The 25 scholars most cited alongside Patrick A. Lundquist, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Patrick A. Lundquist Line = papers co-authored together Patrick A. Lundquist links everyone, so they are left out of the graph.

All Works

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16 of 16 papers shown

#	Work
1	Identification of 58 novel mutations in Niemann-Pick disease type C: Correlation with biochemical phenotype and importance ofPTC1-like domains inNPC1 Human Mutation ·Walter D. Park, John F. O’Brien, Patrick A. Lundquist, Daniel Kraft, Cate Walsh Vockley, Pamela S. Karnes, Marc C. Patterson, Karen Snow	2003	146
2	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 ·Xiaofeng Sun, David L. Marks, Walter D. Park, Christine L. Wheatley, Vishwajeet Puri, John F. O’Brien, Daniel Kraft, Patrick A. Lundquist, Marc C. Patterson, Richard E. Pagano, Karen Snow	2001	115
3	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 ·Carla G. Monico, Sandro Rossetti, Heidi A. Schwanz, Julie B. Olson, Patrick A. Lundquist, D. Brian Dawson, Peter C. Harris, Dawn S. Milliner	2007	53
4	Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy Neurology ·Wei Wang, Chen Wang, D. Brian Dawson, Erik C. Thorland, Patrick A. Lundquist, Bruce W. Eckloff, Yanhong Wu, Saurabh Baheti, Jared M. Evans, Steven S. Scherer, P. James B. Dyck, Christopher J. Klein	2016	42
5	Development and Clinical Implementation of a Combination Deletion PCR and Multiplex Ligation-Dependent Probe Amplification Assay for Detecting Deletions Involving the Human α-Globin Gene Cluster Journal of Molecular Diagnostics ·Benjamin R. Kipp, Samantha Roellinger, Patrick A. Lundquist, W. Edward Highsmith, D. Brian Dawson	2011	25
6	A novel deletion of SNURF/SNRPN exon 1 in a patient with Prader-Willi-like phenotype European Journal of Medical Genetics ·Yang Cao, Susan Alhumaidi, Eissa Faqeih, Beth A. Pitel, Patrick A. Lundquist, Umut Aypar	2017	14
7	Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing Journal of Molecular Diagnostics ·Aruna Rangan, Molly S. Hein, Garrett Jenkinson, Tejaswi Koganti, Ross A. Aleff, Christopher A. Hilker, Joseph H. Blommel, Tavanna R. Porter, Kenneth C. Swanson, Patrick A. Lundquist, Phuong L. Nguyen, Min Shi, Rong He, David S. Viswanatha, Jin Jen, Eric W. Klee, Benjamin R. Kipp, James D. Hoyer, Eric D. Wieben, Jennifer L. Oliveira	2021	10
8	C9orf72 Repeat Expansion Frequency among Patients with Huntington Disease Genetic Testing Neurodegenerative Diseases ·Cristiane M. Ida, Malinda L. Butz, Patrick A. Lundquist, D. Brian Dawson	2018	7
9	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 ·Umut Aypar, Pamela R. Brodersen, Patrick A. Lundquist, D. Brian Dawson, Erik C. Thorland, Nicole L. Hoppman	2014	7
10	Exclusion of a primary gene defect at the HLA locus in familial idiopathic dilated cardiomyopathy. Journal of Medical Genetics ·Timothy M. Olson, Steven Thibodeau, Patrick A. Lundquist, Daniel J. Schaid, Virginia V. Michels	1995	5
11	Development and Validation of a Next-Generation Sequencing Panel for Syndromic and Nonsyndromic Hearing Loss The Journal of Applied Laboratory Medicine ·Malinda L. Butz, Amber McDonald, Patrick A. Lundquist, Mélanie Meyer, Sean C. Harrington, Sarah Kester, Mariam I. Stein, Nipun A. Mistry, Eric Zimmerman Zuckerman, Zhiyv Niu, Lisa A. Schimmenti, Linda Hasadsri, Nicole J. Boczek	2020	4
12	Aminoglycoside induced ototoxicity risk in the cystic fibrosis population: The utility of large‐scale screening Pediatric Pulmonology ·Jaime L. Lopes, Noemi Vidal‐Folch, Patrick A. Lundquist, Lisa A. Schimmenti, Nadir Demirel, Vicki Dean, Janelle A. Olson, Tom Auth, Malinda L. Butz, Katelyn A. Reed, Mark E. Wylam, Jessica R. Balcom, Nicole J. Boczek, Linda Hasadsri	2022	4
13	Development and validation of a comprehensive mutation and deletion detection assay for SDHB, SDHC, and SDHD Clinical Biochemistry ·Dragana Milosevic, Patrick A. Lundquist, Kendall W Cradic, Noemi Vidal‐Folch, Thanh‐Truc Huynh, Karel Pacák, Stefan K. Grebe	2010	3
14	Deletional HPFH Vs. Delta Beta Thalassemia: Closing in on a Possible Hb F Silencer Location Blood ·Molly S. Hein, Kenneth C. Swanson, Patrick A. Lundquist, Joella A Yungerberg, Lea M. Coon, Brian D Dawson, Dragan Jevremović, André M. Oliveira, James D. Hoyer, Jennifer L. Oliveira	2015	3
15	Genetic testing for Niemann-Pick Type C disease Genetics in Medicine ·Karen Snow, W.D. Park, Patrick A. Lundquist, Cate Walsh Vockley, Marc C. Patterson, Pamela S. Karnes, John F. O’Brien	2000	1
16	Large Deletions Involving the Beta Globin Gene Complex: Genotype-Phenotype Correlation of 119 Cases Blood ·Molly S. Hein, Jennifer L. Oliveira, Kenneth C. Swanson, Patrick A. Lundquist, Joella A Yungerberg, Lea M. Coon, Brian D Dawson, Ronald S. Go, Dragan Jevremović, James D. Hoyer	2015	1

About Patrick A. Lundquist

Patrick A. Lundquist is a scholar working on Genetics, Molecular Biology, Hematology, Pediatrics, Perinatology and Child Health and Physiology, having authored 16 papers that have together received 440 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (4 papers), Iron Metabolism and Disorders (4 papers), Prenatal Screening and Diagnostics (3 papers), Lysosomal Storage Disorders Research (3 papers), Epigenetics and DNA Methylation (2 papers), Genetic Syndromes and Imprinting (2 papers), Ear Surgery and Otitis Media (2 papers) and Carbohydrate Chemistry and Synthesis (2 papers). The work is most often cited by research in Physiology (50 citations), Physiology (238 citations), Hematology (51 citations), Genetics (45 citations) and Organic Chemistry (105 citations). Patrick A. Lundquist has collaborated with scholars based in United States and China. Frequent co-authors include Daniel Kraft, Karen Snow, Walter D. Park, Marc C. Patterson, John F. O’Brien, D. Brian Dawson, Pamela S. Karnes, Cate Walsh Vockley, David L. Marks and Vishwajeet Puri. Their work appears in journals such as Journal of Molecular Diagnostics, Blood, Neurodegenerative Diseases, Human Mutation and Journal of the American Society of Nephrology.

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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