Yutaka Furuta

ORCID

Publication Activity (10 Years)

Years Active: 2023-2024
Publications (10 Years): 14

Top Venues

American journal of medical genetics. Part A

This page only lists publications with an associated author ORCID identifier.

Publications

Rory J Tinker, Lisa Bastarache, Kimberly Ezell, Serena M Neumann, Yutaka Furuta, Karee A Morgan, John A Phillips
Data from electronic healthcare records expand our understanding of X-linked genetic diseases. American journal of medical genetics. Part A 194 (5) (2024)
Kimberly M Ezell, Rory J Tinker, Yutaka Furuta, Alican Gulsevin, Lisa Bastarache, Rizwan Hamid, Joy D Cogan, Lynette Rives, Serena Neumann, Brian Corner, Mary Kozuria, John A Phillips, null null
Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant. American journal of medical genetics. Part A 194 (7) (2024)
Rory J Tinker, Lisa Bastarache, Kimberly Ezell, Serena M Neumann, Yutaka Furuta, Karee A Morgan, John A Phillips
Data from electronic healthcare records expand our understanding of X-linked genetic diseases. American journal of medical genetics. Part A (2024)
Rory J Tinker, Lisa Bastarache, Kimberly Ezell, Serena M Neumann, Yutaka Furuta, Karee A Morgan, John A Phillips
Data from electronic healthcare records expand our understanding of X-linked genetic diseases. American journal of medical genetics. Part A 194 (5) (2024)
Rory J Tinker, Lisa Bastarache, Kimberly Ezell, Serena M Neumann, Yutaka Furuta, Karee A Morgan, John A Phillips
Data from electronic healthcare records expand our understanding of X-linked genetic diseases. American journal of medical genetics. Part A 194 (5) (2024)
Kimberly M Ezell, Rory J Tinker, Yutaka Furuta, Alican Gulsevin, Lisa Bastarache, Rizwan Hamid, Joy D Cogan, Lynette Rives, Serena Neumann, Brian Corner, Mary Kozuria, John A Phillips, null null
Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant. American journal of medical genetics. Part A (2024)
Kimberly M Ezell, Rory J Tinker, Yutaka Furuta, Alican Gulsevin, Lisa Bastarache, Rizwan Hamid, Joy D Cogan, Lynette Rives, Serena Neumann, Brian Corner, Mary Kozuria, John A Phillips, null null
Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant. American journal of medical genetics. Part A 194 (7) (2024)
Rory J Tinker, Lisa Bastarache, Kimberly Ezell, Serena M Neumann, Yutaka Furuta, Karee A Morgan, John A Phillips
Data from electronic healthcare records expand our understanding of X-linked genetic diseases. American journal of medical genetics. Part A (2024)
Rory J Tinker, Lisa Bastarache, Kimberly Ezell, Serena M Neumann, Yutaka Furuta, Karee A Morgan, John A Phillips
Data from electronic healthcare records expand our understanding of X-linked genetic diseases. American journal of medical genetics. Part A 194 (5) (2024)
Kimberly M Ezell, Rory J Tinker, Yutaka Furuta, Alican Gulsevin, Lisa Bastarache, Rizwan Hamid, Joy D Cogan, Lynette Rives, Serena Neumann, Brian Corner, Mary Kozuria, John A Phillips, null null
Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant. American journal of medical genetics. Part A (2024)
Kimberly M Ezell, Rory J Tinker, Yutaka Furuta, Alican Gulsevin, Lisa Bastarache, Rizwan Hamid, Joy D Cogan, Lynette Rives, Serena Neumann, Brian Corner, Mary Kozuria, John A Phillips, null null
Undiagnosed Disease Network collaborative approach in diagnosing rare disease in a patient with a mosaic CACNA1D variant. American journal of medical genetics. Part A 194 (7) (2024)
Rory J Tinker, Lisa Bastarache, Kimberly Ezell, Serena M Neumann, Yutaka Furuta, Karee A Morgan, John A Phillips
Data from electronic healthcare records expand our understanding of X-linked genetic diseases. American journal of medical genetics. Part A 194 (5) (2024)
Yutaka Furuta, Erica T Nelson, Serena M Neumann, John A Phillips, Rizwan Hamid, Rory J Tinker, Joy D Cogan, Lynette Rives, John H Newman, null null
A medical odyssey of a 72-year-old man with Charcot-Marie-Tooth disease type 2 newly diagnosed with biallelic variants in SORD gene causing sorbitol dehydrogenase deficiency. American journal of medical genetics. Part A (2023)
Yutaka Furuta, Rory J Tinker, Alican Gulsevin, Serena M Neumann, Rizwan Hamid, Joy D Cogan, Lynette Rives, Qi Liu, Hua-Chang Chen, Karen M Joos, John A Phillips, null null
Probable digenic inheritance of Diamond-Blackfan anemia. American journal of medical genetics. Part A (2023)

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Publication Activity (10 Years)

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Yutaka Furuta