Settara C. Chandrasekharappa - National Human Genome Research Institute (NHGRI), National Institutes of Health (NIH)

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论文共 149 篇作者统计合作学者相似作者

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Genomic Landscape of Patients with Germline RUNX1 Variants and Familial Platelet Disorder with Myeloid Malignancy

Kai Yu,Natalie Deuitch,Matthew Merguerian,Lea Cunningham,Joie Davis,Erica Bresciani,Jamie Diemer,Elizabeth Andrews,Alice Young,Frank Donovan,Raman Sood,Kathleen Craft,Shawn Chong,Settara Chandrasekharappa,Jim Mullikin,Paul P. Liu

BLOOD ADVANCESno. 2 (2024): 497-511

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FANCA C.3624c>t (p.ser1208=) is a Hypomorphic Splice Variant Associated with Delayed Onset of Fanconi Anemia

Ramanagouda Ramanagoudr-Bhojappa,Rebecca Tryon,Francis P. Lach,Frank X. Donovan, Rochelle Maxwell,Allana Rosenberg,Margaret L. MacMillan,John E. Wagner,Arleen D. Auerbach,Agata Smogorzewska,Settara C. Chandrasekharappa

BLOOD ADVANCESno. 4 (2024): 899-908

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Mouse Embryo Fibroblasts Lacking the Tumor Suppressor Menin Show Altered Expression of Extracellular Matrix Protein Genes

Youngmi Ji,Nijaguna B. Prasad,Elizabeth A. Novotny,Sukhbir Kaur,Abdel Elkahloun, Yidong Chen,Rui-Zhu Zhang,Mon-Li Chu,Sunita K. Agarwal,Stephen J. Marx,Francis S. Collins,Settara C. Chandrasekharappa

pubmed（2023）

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A Novel De Novo TP63 Mutation in WholeExome Sequencing of a Syrian Family with Oral Cleft and Ectrodactyly

Claire L. C. Simpson,Danielle C. C. Kimble,Settara C. Chandrasekharappa,Khalid Alqosayer,Emily Holzinger,Blake Carrington,John McElderry,Raman Sood, Ghiath E. Al-Souqi,Hasan Albacha-Hejazi,Joan E. Bailey-Wilson

Molecular genetics & genomic medicine（2023）

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Supplementary Figure 2 from Chromosomal Breakpoints in Primary Colon Cancer Cluster at Sites of Structural Variants in the Genome

Jordi Camps,Marian Grade,Quang Tri Nguyen,Patrick Hörmann,Sandra Becker,Amanda B. Hummon,Virginia Rodriguez,Settara Chandrasekharappa,Yidong Chen,Michael J. Difilippantonio,Heinz Becker,B. Michael Ghadimi,Thomas Ried

crossref（2023）

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Supplementary Figures 1-4 from The Tumor Suppressor Protein Menin Inhibits AKT Activation by Regulating Its Cellular Localization

Yan Wang,Atsushi Ozawa,Shadia Zaman,Nijaguna B. Prasad,Settara C. Chandrasekharappa,Sunita K. Agarwal,Stephen J. Marx

crossref（2023）

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Chromosomal Breakpoints in Primary Colon Cancer Cluster at Sites of Structural Variants in the Genome

Jordi Camps,Marian Grade,Quang Tri Nguyen,Patrick Hoermann,Sandra Becker,Amanda B. Hummon,Virginia Rodriguez,Settara Chandrasekharappa,Yidong Chen,Michael J. Difilippantonio,Heinz Becker,B. Michael Ghadimi,Thomas Ried

pubmed（2023）

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Supplementary Table S1 from Mouse Embryo Fibroblasts Lacking the Tumor Suppressor Menin Show Altered Expression of Extracellular Matrix Protein Genes

Youngmi Ji, N. Rajendra Prasad,Elizabeth A. Novotny, Surinder Kaur, Abdel Elkahloun,Yidong Chen,Ruizhu Zhang, Mon‐Li Chu,Sunita Agarwal, Stephen J. Marx,Francis S. Collins,Settara C. Chandrasekharappa

openalex（2023）

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Supplementary Figure 1 from Chromosomal Breakpoints in Primary Colon Cancer Cluster at Sites of Structural Variants in the Genome

crossref（2023）

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Patterns of Mosaicism for Sequence and Copy-Number Variants Discovered Through Clinical Deep Sequencing of Disease-Related Genes in One Million Individuals

Rebecca Truty,Susan Rojahn,Karen Ouyang, Curtis Kautzer,Michael Kennemer,Daniel Pineda-Alvarez,Britt Johnson,Amanda Stafford,Lina Basel-Salmon,Sulagna Saitta,Anne Slavotinek,Settara C. Chandrasekharappa,Carlos Jose Suarez,Leslie Burnett,Robert L. Nussbaum,Swaroop Aradhya

The American Journal of Human Geneticsno. 4 (2023): 551-564

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