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论文共 21 篇作者统计合作学者相似作者

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Long-Read Sequencing is Required for Precision Diagnosis of Incontinentia Pigmenti
Monica H Wojcik, Robin D Clark,Abdallah F Elias,Casie A Genetti,Jill A Madden, Dana Simpson, Linda Golkar,Miranda Pg Zalusky,Angela L Miller, Araceli Rodriguez,Joy Goffena, Camille A Dash,Nikhita Damaraju, Sophia B Gibson, Sophie Hr Storz, Zachary B Anderson,Jonas A Gustafson,Isabelle Thiffault,Emily G Farrow,Tomi Pastinen,Jasmine Lin, Jennifer Huang, Alan H Beggs,Pankaj B Agrawal, Genomics Research to Elucidate the Genetics of Rare Diseases (GREGoR) Consortium, David T Miller,Danny E Miller
HGG advancespp.100468-100468, (2025)
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P756: Uncovering Disease-Associated SVA Insertions Missed by Routine Clinical Testing
Joy Goffena, Jonas Gustafson, Danny Miller
Genetics in Medicine Open (2025): 103125
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P693: Resolution of Newborn Screening Results Via Targeted Long-Read Sequencing
Cate Paschal, Sunny Ye, Candace Myers, Sydney Ward,Joy Goffena, Sophie Storz, Zach Anderson, Miranda Zalusky,Anna Scott, Danny Miller
Genetics in Medicine Open (2025): 103062
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P655: Performing Long-Read Sequencing from Dried Blood Spot Cards
Sydney Ward,Joy Goffena, Sophie Storz,Miranda Galey,Alexandra Keefe,Cate Paschal,Anna Scott,Danny Miller
Genetics in Medicine Open (2024): 101560
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A Diagnostic Blind Spot: Deep Intronic SVA_E Insertion Identified As the Most Common Pathogenic Variant Associated with Canavan Disease
Carlos A Dominguez Gonzalez,Katrina Bell, Ramakrishnan Rajagopalan,Michelle G de Silva,Aida Lemes, Cristin Zabala, Florencia Perez,Alfredo Cerisola,Arastoo Vossough,Matthew Whitehead, Chloe Cunningham,Natasha Brown, Rebecca Quin,Cas Simons,Eloise Uebergang,Rocio Rius, Meutia Kumaheri, Emma Kotes, Ananya Vohra,Kathleen E Sullivan,Miranda Galey, Zachary Anderson, Sophie Storz, Sydney Ward,Joy Goffena,Jonas A Gustafson, Thomas Conway,Susan M White, Adeline Vanderver, Danny Miller
crossref（2024）
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作者统计

#Papers: 21

#Citation: 237

H-Index: 8

G-Index: 11

Sociability: 5

Diversity: 1

Activity: 2

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