Chaya N. Murali

Also affiliated with Texas Children's Hospital

Biochemistry, Genetics and Molecular BiologyEnergyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 22 papers. Top paper: “Health‐related quality of life in adults with osteogenesis imperfecta”.

Health‐related quality of life in adults with osteogenesis imperfecta

Clinical Genetics(2021)10.1111/cge.13939

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0DataRank · unranked

28 citations

Brady Slater, Salma Musaad, David Cuthbertson, Dianne Nguyen, Alicia Turner +7 more

TRMU deficiency: A broad clinical spectrum responsive to cysteine supplementation

Molecular Genetics and Metabolism(2021)10.1016/j.ymgme.2021.01.005

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0DataRank · unranked

26 citations

Claudia Soler‐Alfonso, Kathleen M. Loomes, Amit A. Shah, Danielle Monteil, Carmencita D. Padilla +3 more

Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2020.12.30.424813

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0DataRank · unranked

3 citations

Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves +39 more

Drosophila functional screening of de novo variants in autism uncovers damaging variants and facilitates discovery of rare neurodevelopmental diseases

Cell Reports(2022)10.1016/j.celrep.2022.110517

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0DataRank · unranked

52 citations

Samantha L. Deal, Jonathan C. Andrews, J. Michael Harnish, Venkata Hemanjani Bhavana, Hillary K. Graves +56 more

Natural history of TANGO2 deficiency disorder: Baseline assessment of 73 patients

Genetics in Medicine(2022)10.1016/j.gim.2022.11.020

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0DataRank · unranked

50 citations

Erica Julianne Lay, Claudia Soler‐Alfonso, Kevin E. Glinton, Kimberly Houck, Mustafa Tosur +29 more

A multicenter study to evaluate pain characteristics in osteogenesis imperfecta

American Journal of Medical Genetics Part A(2022)10.1002/ajmg.a.63009

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0DataRank · unranked

29 citations

Karen M. Kruger, Angela Caudill, Chaya N. Murali, Sandesh C.S. Nagamani, Peter A. Smith +2 more

Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes

Brain(2023)10.1093/brain/awad403

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0DataRank · unranked

27 citations

Allan Bayat, Linda G. Zachariassen, Jiahui Sun, Yu-Han Ge, Dan Zhao +82 more

Heterozygous nonsense variants in the ferritin heavy-chain gene FTH1 cause a neuroferritinopathy

Human Genetics and Genomics Advances(2023)10.1016/j.xhgg.2023.100236

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0DataRank · unranked

17 citations

Jesus A Tintos-Hernández, Chaya N. Murali, Monica Penon‐Portmann, Marco Flores‐Méndez, Adrian Santana +12 more

A multicenter cross-sectional study in infants with congenital heart defects demonstrates high diagnostic yield of genetic testing but variable evaluation practices

Genetics in Medicine Open(2023)10.1016/j.gimo.2023.100814

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0DataRank · unranked

15 citations

Lindsey R. Helvaty, Ming Li, William L. Border, Sara Fitzgerald‐Butt, Vidu Garg +11 more

A qualitative exploration of patient perspectives on psychosocial burdens and positive factors in adults with osteogenesis imperfecta

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63323

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0DataRank · unranked

13 citations

Alyssa Hertz, Andrew D. Wiese, Kristin M. Kostick, Dianne Nguyen, Sophie C. Schneider +8 more

Health-related quality of life in a systematically assessed cohort of children and adults with urea cycle disorders

Molecular Genetics and Metabolism(2023)10.1016/j.ymgme.2023.107696

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6 citations

John R. Barber, Robert McCarter, Anqing Zhang, Natalie M. Gallant, Kara Simpson +7 more

Heterozygous Nonsense Variants in the Ferritin Heavy Chain Gene FTH1 Cause a Novel Pediatric Neuroferritinopathy

medRxiv(2023)10.1101/2023.01.30.23285099

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1 citations

Jesus A Tintos-Hernández, Chaya N. Murali, Monica Penon‐Portmann, Marco Flores‐Méndez, Adrian Santana +12 more

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a severe developmental disorder spectrum

Genetics in Medicine(2024)10.1016/j.gim.2024.101273

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0DataRank · unranked

11 citations

Jovi Huixin Wong, Puravi Panda, Dat Nguyen, Nancy C.P. Leong, Riccardo Sangermano +62 more

Resilience and coping: a qualitative analysis of cognitive and behavioral factors in adults with osteogenesis Imperfecta

Disability and Rehabilitation(2024)10.1080/09638288.2024.2358903

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0DataRank · unranked

5 citations

Whitney S. Shepherd, Gianna M. Colombo, Andrew D. Wiese, W. Conor Rork, Kristin M. Kostick +10 more

The Impact of Cognitive Behavioral Therapy on Sleep Problems in Autistic Children with Co-occurring Anxiety

Journal of Autism and Developmental Disorders(2024)10.1007/s10803-024-06309-2

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0DataRank · unranked

4 citations

Minjee Kook, Peter Boedeker, Andrew G. Gusick, Ariel M. Lyons‐Warren, Robin P. Goin‐Kochel +4 more

Improving access to exome sequencing in a medically underserved population through the Texome Project

Genetics in Medicine(2024)10.1016/j.gim.2024.101102

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0DataRank · unranked

3 citations

Ryan J. German, Seema R. Lalani, Chaya N. Murali, Carlos A. Bacino, Stephanie Baskin +31 more

Qualitative investigation of school experiences in children with osteogenesis imperfecta

Children s Health Care(2024)10.1080/02739615.2024.2403482

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0DataRank · unranked

3 citations

Andrew D. Wiese, Whitney S. Shepherd, Gianna M. Colombo, Selena Guo, Justin Qian +14 more

Biallelic variation in the choline and ethanolamine transporter FLVCR1 underlies a pleiotropic disease spectrum from adult neurodegeneration to severe developmental disorders

medRxiv(2024)10.1101/2024.02.09.24302464

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0DataRank · unranked

2 citations

Jovi Huixin Wong, Puravi Panda, Dat Nguyen, Nancy C.P. Leong, Riccardo Sangermano +57 more

Sequence variants in HECTD1 result in a variable neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.001

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0DataRank · unranked

4 citations

Elias Oxman, Hieu D. Hoang, Wu‐Lin Charng, Tanvitha Kotla, Weimin Yuan +49 more

Variants in BSN, encoding the presynaptic protein Bassoon, result in a distinct neurodevelopmental disorder with a broad phenotypic range

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.04.011

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0DataRank · unranked

4 citations

Sarah M. Ruggiero, Shiva Ganesan, Colin A. Ellis, Abiola Harrison, Katie Rose Sullivan +32 more

Variants in BSN , encoding the presynaptic protein Bassoon, result in a novel neurodevelopmental disorder with a broad phenotypic range

medRxiv(2025)10.1101/2025.02.10.25321755

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0DataRank · unranked

0 citations

Sarah M. Ruggiero, Shiva Ganesan, Colin A. Ellis, Abiola Harrison, Katie Rose Sullivan +34 more

Osteogenesis imperfecta and the family: A qualitative analysis of the experiences of family and caregivers.

Families Systems & Health(2025)10.1037/fsh0001004

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0DataRank · unranked

0 citations

Andrew D. Wiese, Amelia Mercado, Whitney S. Shepherd, Michelle L. Fynan, Kara Ayers +14 more