Haley Streff

ScholarGPS® ID: 53810930978506

Affiliation

Baylor College of Medicine, Houston, United States

Affiliation History

Field

Life Sciences

Discipline

Genetics

Top Specialties

Mutation | Medical Genetics | Neurodevelopmental Disorder

Metrics Summary

Publication Count

Predicted Citations

262

Predicted h-index

Ranking

Publications and Citation History

Publications based on Top Specialties

Types of Publication

Publications
Books
Patents
NIH/NSF

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Perceived impact of ethnocultural competency training on genetic counselors' clinical interactions (journal article) El Achi, Dina \| Brown, Austin \| Huguenard, Sarah \| Khan, Sarah \| Streff, Haley \| Nassef, Salma Journal of Genetic Counseling, volume 33, issue 3, pages 605-614 (2024). 10.1002/jgc4.1756 Cite \| Source
A familial deletion of 10p12.1 associated with thrombocytopenia (journal article) Manohar, Sujal \| Gofin, Yoel \| Streff, Haley \| Vossaert, Liesbeth \| Camacho, Pamela \| Murali, Chaya N. American Journal of Medical Genetics Part A, volume 194, issue 1, pages 77-81 (2024). 10.1002/ajmg.a.63403 Cite \| Source
A novel de novo pathogenic variant in TBL1XR1 as a new proposed cause of Pierpont syndrome (journal article) Tamma, Poornima L. \| Streff, Haley \| Murali, Chaya N. American Journal of Medical Genetics Part A, volume 191, issue 6, pages 1576-1580 (2023). 10.1002/ajmg.a.63162 Cited by (2) \| Cite \| Source
Novel phenotype of aortic root dilatation and late‐onset metabolic decompensation in a patient with TMEM70 deficiency (journal article) Mackay, Laura \| Gijavanekar, Charul \| Streff, Haley \| Price, Jack F. \| Elsea, Sarah H. \| Scaglia, Fernando American Journal of Medical Genetics Part A, volume 191, issue 5, pages 1366-1372 (2023). 10.1002/ajmg.a.63131 Cited by (3) \| Cite \| Source
Cascade testing after exome sequencing: Retrospective analysis of linked family data at 2 US laboratories (journal article) Stefka, Julie \| Streff, Haley \| Liu, Pengfei \| Towne, Meghan \| Smith, Hadley Stevens Genetics in Medicine, volume 25, issue 5, pages 100818- (2023). 10.1016/j.gim.2023.100818 Cited by (1) \| Cite \| Source
Access to clinically indicated genetic tests for pediatric patients with Medicaid: Evidence from outpatient genetics clinics in Texas (journal article) Streff, Haley \| Uhles, Crescenda L. \| Fisher, Heather \| Franciskovich, Rachel \| Littlejohn, Rebecca O. \| Gerard, Amanda \| Hudnall, Julianna \| Smith, Hadley Stevens Genetics in Medicine, volume 25, issue 3, pages 100350- (2023). 10.1016/j.gim.2022.11.018 Cited by (2) \| Cite \| Source
P130: Case report: Phenotypic features among four first-degree relatives with 17q11.2 microduplication syndrome (journal article) Bradley, Catherine \| Streff, Haley \| Bi, Weimin \| Smith, Janice \| Rosenfeld, Jill \| Marom, Ronit Genetics in Medicine Open, volume 1, issue 1, pages 100159- (2023). 10.1016/j.gimo.2023.100159 Cite \| Source
Mutations of the histone linker H1–4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4 (journal article) Tremblay, Martine W \| Green, Matthew V \| Goldstein, Benjamin M \| Aldridge, Andrew I \| Rosenfeld, Jill A \| Streff, Haley \| Tan, Wendy D \| Craigen, William \| Bekheirnia, Nasim \| Al Tala, Saeed \| ... \| Jiang, Yong-hui Human Molecular Genetics, volume 31, issue 9, pages 1430-1442 (2022). 10.1093/hmg/ddab321 Cited by (5) \| Cite \| Source
eP025: Novel phenotype of aortic root dilatation and late onset of metabolic decompensation in patient with TMEM70 deficiency (journal article) Mackay, Laura \| Scaglia, Fernando \| Streff, Haley Genetics in Medicine, volume 24, issue 3, pages S17- (2022). 10.1016/j.gim.2022.01.063 Cite \| Source
eP517: Differences in genetic testing uptake in a large metropolitan pediatric outpatient genetics clinic over time (journal article) Streff, Haley \| Chan, Katie \| Gerard, Amanda \| Ladha, Farah \| Magoulas, Pilar \| Wheeler, Arden \| Franciskovich, Rachel Genetics in Medicine, volume 24, issue 3, pages S330- (2022). 10.1016/j.gim.2022.01.549 Cite \| Source
PPP3CA truncating variants clustered in the regulatory domain cause early‐onset refractory epilepsy (journal article) Panneerselvam, Sugi \| Wang, Julia \| Zhu, Wenmiao \| Dai, Hongzheng \| Pappas, John G. \| Rabin, Rachel \| Low, Karen J. \| Rosenfeld, Jill A. \| Emrick, Lisa \| Xiao, Rui \| ... \| Bi, Weimin Clinical Genetics, volume 100, issue 2, pages 227-233 (2021). 10.1111/cge.13979 Cited by (7) \| Cite \| Source
Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics (journal article) Smith, Hadley Stevens \| Franciskovich, Rachel \| Lewis, Andrea M. \| Gerard, Amanda \| Littlejohn, Rebecca O. \| Nugent, Kimberly \| Rodriguez, Janah \| Streff, Haley Genetics in Medicine, volume 23, issue 5, pages 950-955 (2021). 10.1038/s41436-020-01081-x Cited by (15) \| Cite \| Source
Molecular characterisation of rare loss-of-function NPAS3 and NPAS4 variants identified in individuals with neurodevelopmental disorders (journal article) Rossi, Joseph J. \| Rosenfeld, Jill A. \| Chan, Katie M. \| Streff, Haley \| Nankivell, Victoria \| Peet, Daniel J. \| Whitelaw, Murray L. \| Bersten, David C. Scientific Reports, volume 11, issue 1 (2021). 10.1038/s41598-021-86041-4 Cited by (7) \| Cite \| Source
OTUD5 Variants Associated With X-Linked Intellectual Disability and Congenital Malformation (journal article) Saida, Ken \| Fukuda, Tokiko \| Scott, Daryl A. \| Sengoku, Toru \| Ogata, Kazuhiro \| Nicosia, Annarita \| Hernandez-Garcia, Andres \| Lalani, Seema R. \| Azamian, Mahshid S. \| Streff, Haley \| ... \| Matsumoto, Naomichi Frontiers in Cell and Developmental Biology, volume 9 (2021). 10.3389/fcell.2021.631428 Cited by (4) \| Cite \| Source
TSC1 Variant Associated With Mild or Absent Clinical Features of Tuberous Sclerosis Complex in a Three-Generation Family (journal article) Streff, Haley \| Posey, Jennifer E. \| Mauer, Caitlin B. \| Krempely, Kate \| Potocki, Lorraine \| Northrup, Hope Pediatric Neurology, volume 110 (2020). 10.1016/j.pediatrneurol.2020.04.017 Cited by (3) \| Cite \| Source
Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity (journal article) Asselin, Laure \| Rivera Alvarez, José \| Heide, Solveig \| Bonnet, Camille S. \| Tilly, Peggy \| Vitet, Hélène \| Weber, Chantal \| Bacino, Carlos A. \| Baranaño, Kristin \| Chassevent, Anna \| ... \| Godin, Juliette D. Nature Communications, volume 11, issue 1 (2020). 10.1038/s41467-020-16294-6 Cited by (30) \| Cite \| Source
A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder (journal article) Tessadori, Federico \| Rehman, Atteeq U. \| Giltay, Jacques C. \| Xia, Fan \| Streff, Haley \| Duran, Karen \| Bakkers, Jeroen \| Lalani, Seema R. \| van Haaften, Gijs European Journal of Human Genetics, volume 28, issue 5, pages 674-678 (2020). 10.1038/s41431-019-0552-9 Cited by (9) \| Cite \| Source
Functional evaluation of the C-terminal region of bacteriophage T4 Rad50 (journal article) Streff, Haley E. \| Gao, Yang \| Nelson, Scott W. Biochemical and Biophysical Research Communications, volume 526, issue 2, pages 485-490 (2020). 10.1016/j.bbrc.2020.02.172 Cited by (1) \| Cite \| Source
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder (journal article) Scott, Tiana M. \| Guo, Hui \| Eichler, Evan E. \| Rosenfeld, Jill A. \| Pang, Kaifang \| Liu, Zhandong \| Lalani, Seema \| Bi, Weimin \| Yang, Yaping \| Bacino, Carlos A. \| ... \| Scott, Daryl A. Human Mutation, volume 41, issue 5, pages 921-925 (2020). 10.1002/humu.23992 Cited by (11) \| Cite \| Source
Kenny-Caffey Syndrome Type 2: A Unique Presentation and Craniofacial Analysis (journal article) Turner, Acara E. \| Abu-Ghname, Amjed \| Davis, Matthew J. \| Shih, Linden \| Volk, Angela S. \| Streff, Haley \| Buchanan, Edward P. Journal of Craniofacial Surgery, volume 31, issue 5, pages e471-e475 (2020). 10.1097/SCS.0000000000006439 Cited by (9) \| Cite \| Source