Kurt N. Hetrick

5.9k total citations
12 papers, 555 citations indexed

About

Kurt N. Hetrick is a scholar working on Molecular Biology, Genetics and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Kurt N. Hetrick has authored 12 papers receiving a total of 555 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Kurt N. Hetrick's work include Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Gene expression and cancer classification (3 papers). Kurt N. Hetrick is often cited by papers focused on Genomics and Rare Diseases (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Gene expression and cancer classification (3 papers). Kurt N. Hetrick collaborates with scholars based in United States, United Kingdom and Australia. Kurt N. Hetrick's co-authors include Kimberly F. Doheny, Matthew Flickinger, Jane Romm, Gonçalo R. Abecasis, Michael Boehnke, Goo Jun, Hyun Min Kang, Elizabeth Pugh, Hua Ling and Julie A. Jurgens and has published in prestigious journals such as Bioinformatics, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Kurt N. Hetrick

12 papers receiving 547 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kurt N. Hetrick United States	9	280	250	76	39	37	12	555
Ingrid Simonic United Kingdom	14	331 1.2×	371 1.5×	110 1.4×	11 0.3×	28 0.8×	23	758
Sebastian Eck Germany	12	448 1.6×	366 1.5×	168 2.2×	36 0.9×	28 0.8×	23	1.0k
Juan C. Perín United States	14	189 0.7×	510 2.0×	78 1.0×	23 0.6×	32 0.9×	17	834
Davut Pehli̇van United States	17	508 1.8×	656 2.6×	74 1.0×	40 1.0×	26 0.7×	62	1.1k
Stefan Hartung Germany	16	261 0.9×	360 1.4×	44 0.6×	15 0.4×	26 0.7×	22	980
Katarina Truvé Sweden	15	167 0.6×	258 1.0×	56 0.7×	48 1.2×	57 1.5×	17	542
Daniele Colombo Italy	7	273 1.0×	774 3.1×	103 1.4×	23 0.6×	31 0.8×	9	904
Jessica M. Maia United States	11	476 1.7×	524 2.1×	135 1.8×	15 0.4×	29 0.8×	16	994
Anthi Drousiotou Cyprus	14	368 1.3×	465 1.9×	34 0.4×	29 0.7×	76 2.1×	47	1.1k
Laurent C. Francioli United States	9	573 2.0×	540 2.2×	126 1.7×	13 0.3×	30 0.8×	11	990

Countries citing papers authored by Kurt N. Hetrick

Since Specialization

Citations

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

Fields of papers citing papers by Kurt N. Hetrick

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kurt N. Hetrick. 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 Kurt N. Hetrick. The network helps show where Kurt N. Hetrick may publish in the future.

Co-authorship network of co-authors of Kurt N. Hetrick

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

All Works

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12 of 12 papers shown

Sheridan, Molly B., Melis A. Aksit, Kymberleigh A. Pagel, et al.. (2024). The clinical utility of sequencing the entirety of CFTR. Journal of Cystic Fibrosis. 23(4). 707–715. 1 indexed citations

Raraigh, Karen S., Melis A. Aksit, Kurt N. Hetrick, et al.. (2021). Complete CFTR gene sequencing in 5,058 individuals with cystic fibrosis informs variant-specific treatment. Journal of Cystic Fibrosis. 21(3). 463–470. 17 indexed citations

Marosy, Beth, Kurt N. Hetrick, P. Dane Witmer, et al.. (2017). Generating Exome Enriched Sequencing Libraries from Formalin‐Fixed, Paraffin‐Embedded Tissue DNA for Next‐Generation Sequencing. Current Protocols in Human Genetics. 92(1). 18.10.1–18.10.25. 3 indexed citations

Jurgens, Julie A., Hua Ling, Kurt N. Hetrick, et al.. (2015). Assessment of incidental findings in 232 whole-exome sequences from the Baylor–Hopkins Center for Mendelian Genomics. Genetics in Medicine. 17(10). 782–788. 35 indexed citations

Farlow, Janice L., Hai Lin, Laura Sauerbeck, et al.. (2015). Lessons Learned from Whole Exome Sequencing in Multiplex Families Affected by a Complex Genetic Disorder, Intracranial Aneurysm. PLoS ONE. 10(3). e0121104–e0121104. 119 indexed citations

Sobreira, Nara, Julie A. Jurgens, Hua Ling, et al.. (2014). Novel Deletion of <b><i>SERPINF1</i></b> Causes Autosomal Recessive Osteogenesis Imperfecta Type VI in Two Brazilian Families. Molecular Syndromology. 5(6). 268–275. 19 indexed citations

Hoover‐Fong, Julie, Nara Sobreira, Julie A. Jurgens, et al.. (2014). Mutations in PCYT1A, Encoding a Key Regulator of Phosphatidylcholine Metabolism, Cause Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy. The American Journal of Human Genetics. 94(1). 105–112. 45 indexed citations

Jun, Goo, Matthew Flickinger, Kurt N. Hetrick, et al.. (2012). Detecting and Estimating Contamination of Human DNA Samples in Sequencing and Array-Based Genotype Data. The American Journal of Human Genetics. 91(5). 839–848. 205 indexed citations

Halper‐Stromberg, Eitan, Laurence P. Frelin, Ingo Ruczinski, et al.. (2011). Performance assessment of copy number microarray platforms using a spike-in experiment. Bioinformatics. 27(8). 1052–1060. 18 indexed citations

10.

Pankratz, Nathan, Alexandra Dumitriu, Kurt N. Hetrick, et al.. (2011). Copy Number Variation in Familial Parkinson Disease. PLoS ONE. 6(8). e20988–e20988. 54 indexed citations

11.

Ling, Hua, Kurt N. Hetrick, Joan E. Bailey‐Wilson, & Elizabeth Pugh. (2009). Application of sex-specific single-nucleotide polymorphism filters in genome-wide association data. BMC Proceedings. 3(S7). S57–S57. 6 indexed citations

12.

Ritchie, Matthew E., Benilton S. Carvalho, Kurt N. Hetrick, Simon Tavaré, & Rafael A. Irizarry. (2009). R/Bioconductor software for Illumina's Infinium whole-genome genotyping BeadChips. Bioinformatics. 25(19). 2621–2623. 33 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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