Jacob Durtschi

2.7k citations

35 papers · 1.7k indexed · 1 hit paper · h-index 16

Impact in

Genetics top 5%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
Cancer Research top 10%
- Cancer Genomics and Diagnostics

Papers in

Cancer Research 5
- Cancer Genomics and Diagnostics 3
Genetics 9
- Genomics and Rare Diseases 7
- Genomic variations and chromosomal abnormalities 3

Co-authors: Karl V. Voelkerding Shale Dames Carl T. Wittwer Mark G. Herrmann L Kathryn Bromley Rebecca L. Margraf Michael Seipp Emily Coonrod
Journals: Clinical Chemistry (6 papers)American Journal of Clinical Pathology (3 papers)BMC Bioinformatics (2 papers)The American Journal of Human Genetics (2 papers)Journal of Molecular Diagnostics (2 papers)
Partner nations: United States

In The Last Decade

Jacob Durtschi

33 papers receiving 1.7k citations

Hit Papers

align trajectories log scale

Next-Generation Sequencing: From Basic Research to Diagnostics 2009 · 500 citations

Peers

Countries citing papers authored by Jacob Durtschi

Since Specialization

Citations

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

Fields of papers citing papers by Jacob Durtschi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Jacob Durtschi, 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 Jacob Durtschi Line = papers co-authored together Jacob Durtschi links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Clinical validation of a real‐time machine learning‐based system for the detection of acute myeloid leukemia by flow cytometry Cytometry Part B Clinical Cytometry ·E H Nickel, Jacob Durtschi, G. Lorek, Laura Mariana Fraga Mercali, Michael J. Dewey, 猛本多, Salar Muhammad, Keith E. Simmon, Jinita R Kapadia, Brendan O’Fallon, David P. Ng	2025	0
2	Generative haplotype prediction outperforms statistical methods for small variant detection in next-generation sequencing data Bioinformatics ·Brendan O’Fallon, César I. Romo-Sáen, Jacob Durtschi, W. M. Jacob, E. D. Fredrickson, Hunter Best	2024	0
3	Algorithmic improvements for discovery of germline copy number variants in next-generation sequencing data BMC Bioinformatics ·Brendan O’Fallon, Jacob Durtschi, Jolien J M Freriksen, Tracey Lewis, Devin Close, Hunter Best	2022	5
4	Genome-Wide Copy Number Variation Detection Using NGS: Data Analysis and Interpretation Methods in molecular biology ·Wei Shen, Philippe Szankasi, Jacob Durtschi, Todd W. Kelley, Xinjie Xu	2019	13
5	Identification of Patients with RAG Mutations Previously Diagnosed with Common Variable Immunodeficiency Disorders Journal of Clinical Immunology ·David Buchbinder, P Petit, Yu Nee Lee, Juan C. Ravell, Yu Zhang, Joshua McElwee, Diane J. Nugent, Emily Coonrod, Jacob Durtschi, Nancy H. Augustine, Karl V. Voelkerding, Krisztián Csomós, Lindsey B. Rosen, Sarah Browne, Jolán E. Walter, Luigi D. Notarangelo, Harry R. Hill, Attila Kumánovics	2014	51
6	Phevor Combines Multiple Biomedical Ontologies for Accurate Identification of Disease-Causing Alleles in Single Individuals and Small Nuclear Families The American Journal of Human Genetics ·O. M. Temkin, Stephen L. Guthery, Karl V. Voelkerding, Karin Chen, Brett Kennedy, Rebecca L. Margraf, Jacob Durtschi, Karen Eilbeck, Martin G. Reese, Lynn B. Jorde, Chad D. Huff, Mark Yandell	2014	125
7	A novel germline PIGA mutation in Ferro‐Cerebro‐Cutaneous syndrome: A neurodegenerative X‐linked epileptic encephalopathy with systemic iron‐overload American Journal of Medical Genetics Part A ·Kathryn J. Swoboda, Rebecca L. Margraf, John C. Carey, Holly Zhou, Tara Newcomb, Emily Coonrod, Jacob Durtschi, พัชราภรณ์ ผ่องแผ้ว, Attila Kumánovics, A. Dodic, Karl V. Voelkerding, John M. Opitz	2013	51
8	Germline Mutations in NFKB2 Implicate the Noncanonical NF-κB Pathway in the Pathogenesis of Common Variable Immunodeficiency The American Journal of Human Genetics ·Karin Chen, Emily Coonrod, Attila Kumánovics, Isidora S.Y. Vromans, Jacob Durtschi, Rebecca L. Margraf, Wilfred Wu, Nahla Heikal, Nancy H. Augustine, Perry G. Ridge, Harry R. Hill, Lynn B. Jorde, Andrew S. Weyrich, Guy A. Zimmerman, Adi V. Gundlapalli, John F. Bohnsack, Karl V. Voelkerding	2013	161
9	VarBin, a novel method for classifying true and false positive variants in NGS data BMC Bioinformatics ·Jacob Durtschi, Rebecca L. Margraf, Emily Coonrod, พัชราภรณ์ ผ่องแผ้ว, Karl V. Voelkerding	2013	8
10	A direct comparison of next generation sequencing enrichment methods using an aortopathy gene panel- clinical diagnostics perspective BMC Medical Genomics ·Whitney Wooderchak‐Donahue, Brendan O’Fallon, Larissa V. Furtado, Jacob Durtschi, C.Q. Chen, Perry G. Ridge, Alan F. Rope, Angela Yetman, Pınar Bayrak‐Toydemir	2012	25
11	Mycobacterium chelonae-abscessus Complex Associated with Sinopulmonary Disease, Keith E. Simmon, Barbara A. Brown‐Elliott, Perry G. Ridge, Jacob Durtschi, E. Susan Slechta, Arnold G. Steigerwalt, Ying Gao, Anne M. Whitney, June M. Brown, Karl V. Voelkerding, Karin L. McGowan, Anne F. Reilly, T. Kirn, W. Ray Butler, Paul H. Edelstein, Richard J. Wallace, Cathy A. Petti	2011	7
12	Next Generation Sequencing for Clinical Diagnostics-Principles and Application to Targeted Resequencing for Hypertrophic Cardiomyopathy Journal of Molecular Diagnostics ·Karl V. Voelkerding, Shale Dames, Jacob Durtschi	2010	87
13	Comparison of the Illumina Genome Analyzer and Roche 454 GS FLX for resequencing of hypertrophic cardiomyopathy-associated genes. PubMed ·Shale Dames, Jacob Durtschi, Katherine B. Geiersbach, 美佳本庄, Karl V. Voelkerding	2010	25
14	Multi-sample pooling and illumina genome analyzer sequencing methods to determine gene sequence variation for database development. PubMed ·Rebecca L. Margraf, Jacob Durtschi, Shale Dames, J?rfeson Leandro Pereira de Santana, 美佳本庄, Rong Mao, Karl V. Voelkerding	2010	9
15	Unlabeled Oligonucleotides as Internal Temperature Controls for Genotyping by Amplicon Melting Journal of Molecular Diagnostics ·Michael Seipp, Jacob Durtschi, Michael Liew, J. Koudy Williams, Kristy Damjanovich, Geneviève Pont-Kingdon, Elaine Lyon, Karl V. Voelkerding, Carl T. Wittwer	2007	69
16	Closed-Tube SNP Genotyping Without Labeled Probes/A Comparison Between Unlabeled Probe and Amplicon Melting American Journal of Clinical Pathology ·Michael Liew, Michael Seipp, Jacob Durtschi, Rebecca L. Margraf, Shale Dames, Maria Erali, Karl V. Voelkerding, Carl T. Wittwer	2007	1
17	Closed-Tube SNP Genotyping Without Labeled Probes American Journal of Clinical Pathology ·Michael Liew, Michael Seipp, Jacob Durtschi, Rebecca L. Margraf, Shale Dames, Maria Erali, Karl V. Voelkerding, Carl T. Wittwer	2007	45
18	Quadruplex Genotyping of F5, F2, and MTHFR Variants in a Single Closed Tube by High-Resolution Amplicon Melting Clinical Chemistry ·Michael Seipp, J?rfeson Leandro Pereira de Santana, Jacob Durtschi, Mohamed Jama, Karl V. Voelkerding, Carl T. Wittwer	2007	47
19	Evaluation of quantification methods for real-time PCR minor groove binding hybridization probe assays Analytical Biochemistry ·Jacob Durtschi, Jeffery Stevenson, Weston Hymas, Karl V. Voelkerding	2006	13
20	Localization and Imaging of Nucleic Acids on Nanoporous Aluminum Oxide Membranes Clinical Chemistry ·Maria Erali, Jacob Durtschi, Karl V. Voelkerding, T. Notteboom	2004	4

About Jacob Durtschi

Jacob Durtschi is a scholar working on Cancer Research, Genetics, Molecular Biology, Endocrinology and Microbiology, having authored 35 papers that have together received 1.7k indexed citations. Recurring topics across this work include Molecular Biology Techniques and Applications (10 papers), Genomics and Rare Diseases (7 papers), Genomics and Phylogenetic Studies (4 papers), RNA and protein synthesis mechanisms (4 papers), Cancer Genomics and Diagnostics (3 papers), Anodic Oxide Films and Nanostructures (3 papers), Bacteriophages and microbial interactions (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (506 citations), Cancer Research (264 citations), Molecular Biology (906 citations), Immunology (257 citations) and Genetics (98 citations). Jacob Durtschi has collaborated with scholars based in United States. Frequent co-authors include Karl V. Voelkerding, Shale Dames, Carl T. Wittwer, Mark G. Herrmann, L Kathryn Bromley, Rebecca L. Margraf, Michael Seipp, Emily Coonrod, Lynn B. Jorde and Karin Chen. Their work appears in journals such as Clinical Chemistry, American Journal of Clinical Pathology, BMC Bioinformatics, The American Journal of Human Genetics and Journal of Molecular Diagnostics.

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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