Haley E. Streff

1.5k citations
43 papers · 1.0k · h-index 15

Impact in

  • Genetics top 5%
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Genomic variations and chromosomal abnormalities
  • Neurology
    • Neurofibromatosis and Schwannoma Cases

Papers in

  • Genetics 24
    • Genomics and Rare Diseases 13
    • Genomic variations and chromosomal abnormalities 7
    • Genetics and Neurodevelopmental Disorders 5
    • Craniofacial Disorders and Treatments 3
    • Ocular Disorders and Treatments 3
  • Molecular Biology 21
    • Mitochondrial Function and Pathology 4
    • Genomics and Chromatin Dynamics 4
    • Chromatin Remodeling and Cancer 3
Co-authors
Seema R. Lalani (4 shared papers)Jennifer Keating Litton (1 shared paper)Banu Arun (1 shared paper)Claire N. Singletary (1 shared paper)Yuanqing Ye (1 shared paper)Denise R. Nebgen (1 shared paper)Susan K. Peterson (1 shared paper)Jessica Profato (1 shared paper)
Journals
Genetics in Medicine (10 papers)The American Journal of Human Genetics (3 papers)Human Mutation (3 papers)European Journal of Human Genetics (2 papers)Nature Communications (2 papers)
Partner nations
United StatesNetherlandsCanada

In The Last Decade

Haley E. Streff

40 papers receiving 991 citations

Peers

Haley E. Streff
Comparison fields: 5 of 82
  • Genetics 470
  • Neurology 104
  • Molecular Biology 437
  • Cancer Research 62
  • Cell Biology 72
Replace Yuri Uchiyama with:
Yuri Uchiyama Japan
Eri Imagawa Japan
Luis O. Rohena United States
Andrea Hanson‐Kahn United States
Deborah Morrogh United Kingdom
Tanya Bardakjian United States
Simone Pizzi Italy
Deepa Krishnakumar United Kingdom
Julie L. Lauzon Canada
Sevcan Tuğ Bozdoğan Türkiye
Haley E. Streff relative to Yuri Uchiyama Japan Yuri Uchiyama's profile →
Citations per field
00.5×1.5×2×2.5×
Yuri Uchiyama · 1×
Citations per year

Countries citing papers authored by Haley E. Streff

Since Specialization
Citations

This map shows the geographic impact of Haley E. 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 E. 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 E. Streff more than expected).

Fields of papers citing papers by Haley E. Streff

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 43 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Reanalysis of Clinical Exome Sequencing Data
New England Journal of Medicine ·Pengfei Liu, Linyan Meng, Elizabeth A. Normand, Fan Xia, Xiaofei Song, Andrew R. Ghazi, Jill A. Rosenfeld, Pilar L. Magoulas
2019218
2
Clinical spectrum of individuals with pathogenic N F1 missense variants affecting p.Met1149, p.Arg1276, and p.Lys1423: genotype–phenotype study in neurofibromatosis type 1
Human Mutation ·Magdalena Koczkowska, Tom Callens, Yunjia Chen, Alicia Gomes, Alesha D. Hicks, Angela Sharp, Eric Johns, Kim Armfield Uhas
2019100
3
Haploinsufficiency of the Chromatin Remodeler BPTF Causes Syndromic Developmental and Speech Delay, Postnatal Microcephaly, and Dysmorphic Features
The American Journal of Human Genetics ·Paweł Stankiewicz, Tahir Naeem Khan, Przemysław Szafrański, Leah Slattery, Haley E. Streff, Francesco Vetrini, Jonathan Adam Bernstein, Chester Brown
201770
4
De Novo Variants in the ATPase Module of MORC2 Cause a Neurodevelopmental Disorder with Growth Retardation and Variable Craniofacial Dysmorphism
The American Journal of Human Genetics ·María J. Guillen Sacoto, Iva A. Tchasovnikarova, Erin E. Torti, Cara Forster, E. Hallie Andrew, Irina A. Anselm, Kristin W. Baranano, Lauren C. Briere
202068
5
Phenotypic and molecular characterisation of CDK13-related congenital heart defects, dysmorphic facial features and intellectual developmental disorders
Genome Medicine ·Bret L. Bostwick, Scott McLean, Jennifer Ellen Posey, Haley E. Streff, Karen Webster Gripp, Alyssa Blesson, Nina Powell‐Hamilton, Jessica Tusi
201758
6
De novo mutations in MED13, a component of the Mediator complex, are associated with a novel neurodevelopmental disorder
Human Genetics ·Lot Snijders Blok, Susan M. Hiatt, Kevin M. Bowling, Jeremy W. Prokop, Krysta L. Engel, J. Nicholas Cochran, Elizabeth Martina Bebin, Emilia K. Bijlsma
201857
7
Aberrant Function of the C-Terminal Tail of HIST1H1E Accelerates Cellular Senescence and Causes Premature Aging
The American Journal of Human Genetics ·Elisabetta Flex, Simone Martinelli, Anke Van Dijck, Andrea Ciolfi, Serena Cecchetti, Elisa Coluzzi, Luca Pannone, C Andreoli
201951
8
Cancer Incidence in First- and Second-Degree Relatives of BRCA1 and BRCA2 Mutation Carriers
The Oncologist ·Haley E. Streff, Jessica Profato, Yuanqing Ye, Denise R. Nebgen, Susan K. Peterson, Claire N. Singletary, Banu Arun, Jennifer Keating Litton
201643
9
De Novo Truncating Mutations in the Kinetochore-Microtubules Attachment GeneCHAMP1Cause Syndromic Intellectual Disability
Human Mutation ·Bertrand Isidor, Sébastien Küry, Jill A. Rosenfeld, Thomas Besnard, Sébastien Schmitt, Shelagh K. Joss, Sally J Davies, Robert Roger Lebel
201640
10
Mutations in the KIF21B kinesin gene cause neurodevelopmental disorders through imbalanced canonical motor activity
Nature Communications ·Laure Asselin, José Rivera Alvarez, Solveig Heide, Camille S. Bonnet, Peggy Tilly, Hélène Vitet, C. R. Weber, Carlos A. Bacino
202034
11
Outcomes of prior authorization requests for genetic testing in outpatient pediatric genetics clinics
Genetics in Medicine ·Hadley Stevens Smith, Rachel Franciskovich, Andrea M. Lewis, Amanda Gerard, Rebecca Okashah Littlejohn, Kimberly Margaret Nugent, Janah Rodriguez, Haley E. Streff
202125
12
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 ·Nishitha R. Pillai, Noura Al Dhaheri, Rajarshi Ghosh, Jaehyung Lim, Haley E. Streff, Anuranjita Nayak, Brett H. Graham, Neil A. Hanchard
201919
13
FOXI3 pathogenic variants cause one form of craniofacial microsomia
Nature Communications ·Ke Mao, Christelle Borel, Muhammad Ansar, Angad Jolly, Periklis Makrythanasis, Christine Froehlich, Justyna Iwaszkiewicz, Bingqing Wang
202318
14
The first reported case of an inherited pathogenic CHD2 variant in a clinically affected mother and daughter
American Journal of Medical Genetics Part A ·Andrea Klunder Petersen, Haley E. Streff, Mari Tokita, Bret L. Bostwick
201817
15
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 ·Haley E. Streff, Weimin Bi, Athos G. Colón, Adekunle M. Adesina, Christina Y. Miyake, Seema R. Lalani
201816
16
Retrospective analysis of a clinical exome sequencing cohort reveals the mutational spectrum and identifies candidate disease–associated loci for BAFopathies
Genetics in Medicine ·Chun‐An Chen, John Lattier, Wenmiao Zhu, Jill A. Rosenfeld, Lei Wang, Tiana M. Scott, Haowei Du, Vipulkumar Patel
202115
17
BAZ2B haploinsufficiency as a cause of developmental delay, intellectual disability, and autism spectrum disorder
Human Mutation ·Tiana M. Scott, Hui Guo, Evan E. Eichler, Jill A. Rosenfeld, Kaifang Pang, Zhandong Liu, Seema R. Lalani, Weimin Bi
202015
18
Haploinsufficiency of PRR12 causes a spectrum of neurodevelopmental, eye, and multisystem abnormalities
Genetics in Medicine ·Fuad Chowdhury, Lei Wang, Mohammed Al‐Raqad, David J. Amor, Alice Baxová, Šárka Bendová, Elisa Biamino, Alfredo Brusco
202114
19
CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalities
American Journal of Medical Genetics Part A ·Magalie S. Leduc, Zhiyv Niu, Weimin Bi, Wenmiao Zhu, Irene Miloslavskaya, Theodore Chiang, Haley E. Streff, John R. Seavitt
201614
20
A de novo variant in the human HIST1H4J gene causes a syndrome analogous to the HIST1H4C-associated neurodevelopmental disorder
European Journal of Human Genetics ·Federico Tessadori, Atteeq Ur Rehman, Jacques C. Giltay, Fan Xia, Haley E. Streff, Karen J. Duran, Jeroen Bakkers, Seema R. Lalani
201914

About Haley E. Streff

Haley E. Streff is a scholar working on Genetics, Molecular Biology, Physiology, Clinical Biochemistry and Cell Biology, having authored 43 papers that have together received 1.0k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (13 papers), Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (5 papers), Mitochondrial Function and Pathology (4 papers), Genomics and Chromatin Dynamics (4 papers), Craniofacial Disorders and Treatments (3 papers), Chromatin Remodeling and Cancer (3 papers) and Ocular Disorders and Treatments (3 papers). The work is most often cited by research in Genetics (470 citations), Neurology (104 citations), Molecular Biology (437 citations), Cancer Research (62 citations) and Cell Biology (72 citations). Haley E. Streff has collaborated with scholars based in United States, Netherlands and Canada. Frequent co-authors include Seema R. Lalani, Jennifer Keating Litton, Banu Arun, Claire N. Singletary, Yuanqing Ye, Denise R. Nebgen, Susan K. Peterson, Jessica Profato, Hadley Stevens Smith and Weimin Bi. Their work appears in journals such as Genetics in Medicine, The American Journal of Human Genetics, Human Mutation, European Journal of Human Genetics and Nature Communications.

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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