Ulrich Broeckel

15.6k total citations · 1 hit paper
95 papers, 3.9k citations indexed

About

Ulrich Broeckel is a scholar working on Genetics, Molecular Biology and Pharmacology. According to data from OpenAlex, Ulrich Broeckel has authored 95 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Genetics, 27 papers in Molecular Biology and 22 papers in Pharmacology. Recurrent topics in Ulrich Broeckel's work include Pharmacogenetics and Drug Metabolism (22 papers), Genetic Associations and Epidemiology (19 papers) and Genomics and Rare Diseases (9 papers). Ulrich Broeckel is often cited by papers focused on Pharmacogenetics and Drug Metabolism (22 papers), Genetic Associations and Epidemiology (19 papers) and Genomics and Rare Diseases (9 papers). Ulrich Broeckel collaborates with scholars based in United States, Germany and Canada. Ulrich Broeckel's co-authors include Kristine R. Crews, Mary V. Relling, William E. Evans, James M. Hoffman, Heribert Schunkert, Scott C. Howard, Donna K. Arnett, Howard J. Jacob, Amy Turner and Cyrine E. Haidar and has published in prestigious journals such as Circulation, Nature Communications and Nature Genetics.

In The Last Decade

Ulrich Broeckel

93 papers receiving 3.8k 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.

Preemptive Clinical Pharmacogenetics Implementation: Current Programs in Five US Medical Centers

2014 345 citations Kristine R. Crews, James M. Hoffman et al. profile →

Peers

Countries citing papers authored by Ulrich Broeckel

Since Specialization

Citations

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

Fields of papers citing papers by Ulrich Broeckel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ulrich Broeckel

This figure shows the co-authorship network connecting the top 25 collaborators of Ulrich Broeckel. A scholar is included among the top collaborators of Ulrich Broeckel 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 Ulrich Broeckel. Ulrich Broeckel 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

#	Work	Indexed citations
1	Detection of Constitutional Structural Variants by Optical Genome Mapping 2024 ·Journal of Molecular Diagnostics ·Ulrich Broeckel, M. Anwar Iqbal, Brynn Levy, Nikhil Sahajpal, Péter L. Nagy, Gunter Scharer, Vanessa Rodríguez‐Fanjul, Aaron Bossler, Aaron A. Stence, Cindy Skinner, Steven A. Skinner, Ravindra Kolhe, Roger E. Stevenson	8
2	Characterization of Reference Materials for CYP3A4 and CYP3A5 2023 ·Journal of Molecular Diagnostics ·Andrea Gaedigk, Erin C. Boone, Amy Turner, Ron H. N. van Schaik, (unknown), (unknown), Ulrich Broeckel, (unknown), Jennelle C. Hodge, Reynold C. Ly, (unknown), Matthew W. Mitchell, Ann M. Moyer, (unknown), Lisa V. Kalman	8
3	Updated DPYDHapB3 haplotype structure and implications for pharmacogenomic testing 2023 ·Clinical and Translational Science ·Amy Turner, Cyrine E. Haidar, Wenjian Yang, Erin C. Boone, Steven M. Offer, Philip E. Empey, (unknown), (unknown), Gunter Scharer, Ulrich Broeckel, Andrea Gaedigk	23
4	Characterization of complex structural variation in the CYP2D6-CYP2D7-CYP2D8 gene loci using single-molecule long-read sequencing 2023 ·Frontiers in Pharmacology ·Amy Turner, (unknown), Andrea Gaedigk, Mark E. Berres, (unknown), (unknown), Ulrich Broeckel, Gunter Scharer	8
5	Enhancing the functional maturity of hiPSC-derived cardiomyocytes to assess inotropic compounds 2023 ·Journal of Pharmacological and Toxicological Methods ·(unknown), Praful Aggarwal, Ulrich Broeckel, Yama Abassi	2
6	Characterization of Reference Materials for TPMT and NUDT15 2022 ·Journal of Molecular Diagnostics ·Victoria M. Pratt, (unknown), Erin C. Boone, Ulrich Broeckel, Neal Cody, Lisa Edelmann, Andrea Gaedigk, (unknown), (unknown), Ann M. Moyer, Matthew W. Mitchell, Stuart A. Scott, Petr Starostik, Amy Turner, Lisa V. Kalman	11
7	Progress and Research Priorities in Imaging Genomics for Heart and Lung Disease: Summary of an NHLBI Workshop 2021 ·Circulation Cardiovascular Imaging ·Matthew Nayor, Li Shen, Gary M. Hunninghake, Peter Kochunov, R. Graham Barr, David A. Bluemke, Ulrich Broeckel, Peter Caravan, Susan Cheng, Paul S. de Vries, Udo Hoffmann, Márton Kolossváry, Huiqing Li, James Luo, Elizabeth M. McNally, George Thanassoulis, Donna K. Arnett, Ramachandran S. Vasan	3
8	Characterization of Reference Materials with an Association for Molecular Pathology Pharmacogenetics Working Group Tier 2 Status: CYP2C9, CYP2C19, VKORC1, CYP2C Cluster Variant, and GGCX 2021 ·Journal of Molecular Diagnostics ·Victoria M. Pratt, Amy Turner, Ulrich Broeckel, D. Brian Dawson, Andrea Gaedigk, (unknown), (unknown), Ann M. Moyer, (unknown), Francesco Vetrini, Lisa V. Kalman	11
9	Age‐ and Genotype‐Dependent Variability in the Protein Abundance and Activity of Six Major Uridine Diphosphate‐Glucuronosyltransferases in Human Liver 2018 ·Clinical Pharmacology & Therapeutics ·Deepak Bhatt, Aanchal Mehrotra, Andrea Gaedigk, (unknown), Abdul Basit, (unknown), (unknown), Mikael Boberg, Robin E. Pearce, Roger Gaedigk, Ulrich Broeckel, J. Steven Leeder, Bhagwat Prasad	90
10	Pharmacogenetics for Safe Codeine Use in Sickle Cell Disease 2016 ·PEDIATRICS ·Roseann S. Gammal, Kristine R. Crews, Cyrine E. Haidar, James M. Hoffman, Donald K. Baker, (unknown), Jeremie H. Estepp, Deqing Pei, Ulrich Broeckel, Winfred C. Wang, Mitchell J. Weiss, Mary V. Relling, Jane S. Hankins	56
11	PG4KDS: A model for the clinical implementation of pre‐emptive pharmacogenetics 2014 ·American Journal of Medical Genetics Part C Seminars in Medical Genetics ·James M. Hoffman, Cyrine E. Haidar, Mark R. Wilkinson, Kristine R. Crews, Donald K. Baker, Nancy M. Kornegay, Wenjian Yang, Ching‐Hon Pui, Ulrike M. Reiss, Aditya H. Gaur, Scott C. Howard, William E. Evans, Ulrich Broeckel, Mary V. Relling	205
12	RNA Expression Profiling of Human iPSC-Derived Cardiomyocytes in a Cardiac Hypertrophy Model 2014 ·PLoS ONE ·Praful Aggarwal, Amy Turner, Andrea Matter, Steven Kattman, Alexander J. Stoddard, Rachel Lorier, Bradley Jay Swanson, Donna K. Arnett, Ulrich Broeckel	43
13	Whole-exome Sequencing and an iPSC-Derived Cardiomyocyte Model Provides a Powerful Platform for Gene Discovery in Left Ventricular Hypertrophy 2012 ·Frontiers in Genetics ·(unknown), Marguerite R. Irvin, C. Charles Gu, Alexander J. Stoddard, Rachel Lorier, Andrea Matter, D. C. Rao, Vinodh Srinivasasainagendra, Hemant K. Tiwari, Amy Turner, Ulrich Broeckel, Donna K. Arnett	16
14	Cystic fibrosis mutations for p.F508del compound heterozygotes predict sweat chloride levels and pancreatic sufficiency 2011 ·Clinical Genetics ·Ronnie Sebro, Hara Levy, (unknown), David Dimmock, (unknown), Carolyn L. Cannon, Ulrich Broeckel, (unknown)	14
15	Genome-wide association study identifies single-nucleotide polymorphism in KCNB1 associated with left ventricular mass in humans: The HyperGEN Study 2009 ·BMC Medical Genetics ·Donna K. Arnett, Na Li, Weihong Tang, D. C. Rao, Richard B. Devereux, Steven A. Claas, (unknown), Ulrich Broeckel	36
16	Linkage Analysis for Complex Diseases Using Variance Component Analysis 2006 ·Methods in molecular medicine ·Ulrich Broeckel, Karen Colbert Maresso, Lisa J. Martin	2
17	Evidence of transmission ratio distortion of DLG5 R30Q variant in general and implication of an association with Crohn disease in men 2006 ·Human Genetics ·Frauke Friedrichs, Sonia Brescianini, Vito Annese, Anna Latiano, K. C. Berger, Subra Kugathasan, Ulrich Broeckel, Susanna Nikolaus, Mark J. Daly, Stefan Schreiber, John D. Rioux, Monika Stoll	55
18	Toward the Etiologies of Congenital Heart Diseases 2005 ·Clinics in Perinatology ·Andrew N. Pelech, Ulrich Broeckel	8
19	Localization of a Small Genomic Region Associated with Elevated ACE 2000 ·The American Journal of Human Genetics ·Xiaofeng Zhu, Colin A. McKenzie, Terrence Forrester, Deborah A. Nickerson, Ulrich Broeckel, Heribert Schunkert, Angela Doering, Howard J. Jacob, Stephen S. Rich, Mark J. Rieder	99
20	The associations of body size and body composition with left ventricular mass: impacts for indexation in adults 1998 ·Journal of the American College of Cardiology ·Hans‐Werner Hense, (unknown), M Muscholl, Ulrich Broeckel, Bernhard Kuch, Angela Doering, Günter A.J. Riegger, Heribert Schunkert	120

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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