Haley Streff

1.4k total citations
24 papers, 188 citations indexed

About

Haley Streff is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Haley Streff has authored 24 papers receiving a total of 188 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 13 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Haley Streff's work include Genomics and Rare Diseases (11 papers), BRCA gene mutations in cancer (5 papers) and Ocular Disorders and Treatments (3 papers). Haley Streff is often cited by papers focused on Genomics and Rare Diseases (11 papers), BRCA gene mutations in cancer (5 papers) and Ocular Disorders and Treatments (3 papers). Haley Streff collaborates with scholars based in United States, China and Hong Kong. Haley Streff's co-authors include Seema R. Lalani, Claire N. Singletary, Susan K. Peterson, Denise Nebgen, Jennifer K. Litton, Banu Arun, Jessica Profato, Yuanqing Ye, Andrea Petersen and Mari Tokita and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Biochemical and Biophysical Research Communications.

In The Last Decade

Haley Streff

20 papers receiving 184 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Haley Streff United States 9 100 93 23 19 16 24 188
Monika Weisz Hubshman Israel 6 79 0.8× 108 1.2× 18 0.8× 8 0.4× 11 0.7× 7 165
Haktan Bağış Erdem Türkiye 9 68 0.7× 53 0.6× 11 0.5× 9 0.5× 14 0.9× 34 161
Yannis Duffourd France 10 115 1.1× 132 1.4× 17 0.7× 13 0.7× 6 0.4× 25 221
Yoko Hiraki Japan 10 97 1.0× 131 1.4× 11 0.5× 13 0.7× 6 0.4× 17 219
Mullin H.C. Yu Hong Kong 8 87 0.9× 114 1.2× 15 0.7× 10 0.5× 6 0.4× 15 188
Salima El Chehadeh-Djebbar France 4 72 0.7× 154 1.7× 12 0.5× 10 0.5× 10 0.6× 4 222
Yannis Duffourd France 7 125 1.3× 201 2.2× 10 0.4× 14 0.7× 14 0.9× 8 266
Joseph Hostyk United States 5 86 0.9× 85 0.9× 5 0.2× 17 0.9× 14 0.9× 7 177
Margit Nõukas Estonia 9 104 1.0× 111 1.2× 15 0.7× 15 0.8× 8 0.5× 16 216
Fabio Sirchia Italy 9 103 1.0× 108 1.2× 16 0.7× 8 0.4× 7 0.4× 35 208

Countries citing papers authored by Haley Streff

Since Specialization
Citations

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

Fields of papers citing papers by Haley Streff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Haley Streff

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

All Works

20 of 20 papers shown
1.
2.
Streff, Haley, et al.. (2023). A familial deletion of 10p12.1 associated with thrombocytopenia. American Journal of Medical Genetics Part A. 194(1). 77–81.
3.
Streff, Haley, et al.. (2023). A novel de novo pathogenic variant in TBL1XR1 as a new proposed cause of Pierpont syndrome. American Journal of Medical Genetics Part A. 191(6). 1576–1580. 2 indexed citations
4.
Kumar, Runjun D., et al.. (2023). Clinical genome sequencing: Three years’ experience at a tertiary children’s hospital. Genetics in Medicine. 25(10). 100916–100916. 4 indexed citations
5.
Streff, Haley, et al.. (2023). Cascade testing after exome sequencing: Retrospective analysis of linked family data at 2 US laboratories. Genetics in Medicine. 25(5). 100818–100818. 1 indexed citations
6.
Streff, Haley, et al.. (2023). P564: Genetic test stewardship for clinical exome sequencing: Review of critical care orders at Texas Children’s Hospital. SHILAP Revista de lepidopterología. 1(1). 100611–100611.
7.
Streff, Haley, et al.. (2022). Access to clinically indicated genetic tests for pediatric patients with Medicaid: Evidence from outpatient genetics clinics in Texas. Genetics in Medicine. 25(3). 100350–100350. 4 indexed citations
8.
9.
Wang, Julia, Wenmiao Zhu, Hongzheng Dai, et al.. (2021). PPP3CA truncating variants clustered in the regulatory domain cause early‐onset refractory epilepsy. Clinical Genetics. 100(2). 227–233. 11 indexed citations
10.
Smith, Hadley Stevens, Andrea M. Lewis, Amanda Gerard, et al.. (2021). Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics. Genetics in Medicine. 23(5). 950–955. 19 indexed citations
11.
Tremblay, Martine, Andrew Aldridge, Jill A. Rosenfeld, et al.. (2021). Mutations of the histone linker H1–4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4. Human Molecular Genetics. 31(9). 1430–1442. 8 indexed citations
12.
Rosenfeld, Jill A., et al.. (2021). Molecular characterisation of rare loss-of-function NPAS3 and NPAS4 variants identified in individuals with neurodevelopmental disorders. Scientific Reports. 11(1). 6602–6602. 8 indexed citations
13.
Saida, Ken, Tokiko Fukuda, Daryl A. Scott, et al.. (2021). OTUD5 Variants Associated With X-Linked Intellectual Disability and Congenital Malformation. Frontiers in Cell and Developmental Biology. 9. 631428–631428. 6 indexed citations
14.
Streff, Haley, Yang Gao, & Scott W. Nelson. (2020). Functional evaluation of the C-terminal region of bacteriophage T4 Rad50. Biochemical and Biophysical Research Communications. 526(2). 485–490. 1 indexed citations
15.
Abu‐Ghname, Amjed, et al.. (2020). Kenny-Caffey Syndrome Type 2: A Unique Presentation and Craniofacial Analysis. Journal of Craniofacial Surgery. 31(5). e471–e475. 9 indexed citations
16.
Bizargity, Peyman, Haley Streff, Yi-Shan Lee, et al.. (2019). GNA11 brain somatic pathogenic variant in an individual with phacomatosis pigmentovascularis. Neurology Genetics. 5(6). e366–e366. 2 indexed citations
17.
Tessadori, Federico, Atteeq U. Rehman, Jacques C. Giltay, et al.. (2019). A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder. European Journal of Human Genetics. 28(5). 674–678. 11 indexed citations
18.
Pillai, Nishitha R., Rajarshi Ghosh, Haley Streff, et al.. (2019). Biallelic variants in COX4I1 associated with a novel phenotype resembling Leigh syndrome with developmental regression, intellectual disability, and seizures. American Journal of Medical Genetics Part A. 179(10). 2138–2143. 16 indexed citations
19.
Streff, Haley, et al.. (2018). Amish nemaline myopathy and dilated cardiomyopathy caused by a homozygous contiguous gene deletion of TNNT1 and TNNI3 in a Mennonite child. European Journal of Medical Genetics. 62(11). 103567–103567. 15 indexed citations
20.
Streff, Haley, Jessica Profato, Yuanqing Ye, et al.. (2016). Cancer Incidence in First- and Second-Degree Relatives of BRCA1 and BRCA2 Mutation Carriers. The Oncologist. 21(7). 869–874. 37 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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