Akiko Shimamura

Also affiliated with Harvard Stem Cell Institute, Dana-Farber/Boston Children's Cancer and Blood Disorders Center

Biochemistry, Genetics and Molecular BiologyImmunology and MicrobiologyMedicine

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 3%percentile

1.3Author DataRank

Indexed papers

4in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 4 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Association of unbalanced translocation der(1;7) with germline GATA2 mutations

Blood(2021)10.1182/blood.2021012781

Top 32%

0.626DataRank

Top 32%21 citations

Gudrun Göhring, Dennis D. Hickstein, Katherine R. Calvo, Courtney D. DiNardo, Michael Dworzak +42 more

Papers

Driven by 28 papers — median percentile 41. Top paper: “Association of unbalanced translocation der(1;7) with germline GATA2 mutations”.

Association of unbalanced translocation der(1;7) with germline GATA2 mutations

Blood(2021)10.1182/blood.2021012781

Top 32%

0.626DataRank

Top 32%21 citations

Gudrun Göhring, Dennis D. Hickstein, Katherine R. Calvo, Courtney D. DiNardo, Michael Dworzak +42 more

Hospital-wide access to genomic data advanced pediatric rare disease research and clinical outcomes

npj Genomic Medicine(2024)10.1038/s41525-024-00441-9

Top 48%

0.373DataRank

Top 48%11 citations

Nancy C. Andrews, Alan H. Beggs, Philip M. Boone, Catherine A. Brownstein, Maya Chopra +32 more

Distinct genetic pathways define pre-leukemic and compensatory clonal hematopoiesis in Shwachman-Diamond syndrome

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.06.04.134692

N/A

0.292DataRank · unranked

6 citations

Kasiani C. Myers, James R. Bowman, Christopher J. Gibson, Nicholas D. Camarda, Elissa Furutani +38 more

Diagnostic Implications and Correlates of Plasma Adenosine Deaminase 2 Activity and ADA2 Variants

Arthritis & Rheumatology(2025)10.1002/art.43412

Top 70%

0.165DataRank

Top 70%2 citations

Courtney E LeSon, Casey A. Rimland, Kailey Brodeur, Rachel Weng, Evan E. Hsu +51 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

medRxiv(2024)10.1101/2024.12.22.24319370

N/A

0.104DataRank · unranked

1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +30 more

Growth Patterns in Shwachman-Diamond Syndrome: Findings from the North American Shwachman-Diamond Syndrome Registry

The Journal of Pediatrics(2025)10.1016/j.jpeds.2025.114780

Top 78%

0.104DataRank

Top 78%1 citations

Leah Cheng, Sarah K. Steltz, Diana Schwarz, Elizabeth Korn, Sara Loveless +8 more

The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations

Molecular Cytogenetics(2021)10.1186/s13039-021-00575-w

N/A

0DataRank · unranked

16 citations

Alyssa L. Kennedy, Elissa Furutani, Kasiani C. Myers, Annalisa Frattini, Francesco Acquati +11 more

Low frequency of treatable pediatric disease alleles in gnomAD: An opportunity for future genomic screening of newborns

Human Genetics and Genomics Advances(2021)10.1016/j.xhgg.2021.100059

N/A

0DataRank · unranked

12 citations

Steven M. Harrison, Jared H. Rowe, Jessica I. Gold, Elissa Furutani, Alessandra Biffi +5 more

Molecular alterations governing predisposition to myelodysplastic syndromes: Insights from Shwachman-Diamond syndrome

Best Practice & Research Clinical Haematology(2021)10.1016/j.beha.2021.101252

N/A

0DataRank · unranked

4 citations

Akiko Shimamura

Translational research for bone marrow failure patients

Experimental Hematology(2021)10.1016/j.exphem.2021.11.004

N/A

0DataRank · unranked

4 citations

Stephen J. Loughran, Adam C. Wilkinson, Akiko Shimamura, Paula Rı́o, Camille Malouf

DPP9 deficiency: An inflammasomopathy that can be rescued by lowering NLRP1/IL-1 signaling

Science Immunology(2022)10.1126/sciimmunol.abi4611

N/A

0DataRank · unranked

51 citations

Kim S. Robinson, Kenneth Lay, Jasmine C. Wong, Ricardo Moreno Traspas, Nasrin Nabavizadeh +24 more

Pathogenicity and impact of HLA class I alleles in aplastic anemia patients of different ethnicities

JCI Insight(2022)10.1172/jci.insight.163040

N/A

0DataRank · unranked

25 citations

Benjamin F. Frost, Jamie L. Duke, Marian Dribus, Hongbo M. Xie, Zachary D. Prudowsky +28 more

Metformin for treatment of cytopenias in children and young adults with Fanconi anemia

Blood Advances(2022)10.1182/bloodadvances.2021006490

N/A

0DataRank · unranked

16 citations

Elissa Furutani, Shanshan Liu, Erica B. Esrick, Laurie E. Cohen, Jacob R. Bledsoe +29 more

Bringing Patient and Caregivers Voices to the Clinical Trial Chorus: A Report From the BMT CTN Patient and Caregiver Advocacy Task Force

Transplantation and Cellular Therapy(2022)10.1016/j.jtct.2022.10.016

N/A

0DataRank · unranked

9 citations

Shernan G. Holtan, Akiko Shimamura, Todd Burnworth, Shauna Whisenton, Sanderson Adams +8 more

Expanded phenotypic and hematologic abnormalities beyond bone marrow failure in MECOM‐associated syndromes

American Journal of Medical Genetics Part A(2023)10.1002/ajmg.a.63208

N/A

0DataRank · unranked

18 citations

Alison A. Bertuch, Zeinab Afify, Kaylee Dollerschell, Joanne I. Hsu, Tami John +7 more

Treatment of recurrent pediatric myelodysplastic syndrome post hematopoietic stem cell transplantation

Clinical Case Reports(2023)10.1002/ccr3.8190

N/A

0DataRank · unranked

2 citations

Yana Pikman, Jacob R. Bledsoe, Malika Kapadia, Susanne H.C. Baumeister, Jared H. Rowe +8 more

Heterozygous loss-of-function SMC3 variants are associated with variable and incompletely penetrant growth and developmental features

medRxiv(2023)10.1101/2023.09.27.23294269

N/A

0DataRank · unranked

1 citations

Kamli N. W. Faour, Akiko Shimamura, Graeme R. Grimes, Emeline M. Kao, Erica R. Denhoff +50 more

Regulated GATA1 expression as a universal gene therapy for Diamond-Blackfan anemia

Cell stem cell(2024)10.1016/j.stem.2024.10.012

N/A

0DataRank · unranked

19 citations

Xiaotian Liao, Alexis Caulier, Mateusz Antoszewski, Blake Cohen, Myriam Armant +18 more

Heterozygous loss-of-function SMC3 variants are associated with variable growth and developmental features

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100273

N/A

0DataRank · unranked

3 citations

Kamli N. W. Faour, Akiko Shimamura, Graeme R. Grimes, Emeline M. Kao, Erica R. Denhoff +51 more

A methyltransferase-independent role for METTL1 in tRNA aminoacylation and oncogenic transformation

Molecular Cell(2025)10.1016/j.molcel.2025.01.003

N/A

0DataRank · unranked

10 citations

Esteban A. Orellana, Su Hyun Lee, Yun‐Cheol Chae, Yantao Chen, Jim Clauwaert +16 more

Age-dependent phenotypic and molecular evolution of pediatric MDS arising from GATA2 deficiency

Blood Cancer Journal(2025)10.1038/s41408-025-01309-6

N/A

0DataRank · unranked

9 citations

Emilia J. Kozyra, Guolian Kang, Brigitte Strahm, Ayami Yoshimi, Sushree Sangita Sahoo +42 more

On-chip recapitulation of clinical bone marrow toxicities and patient-specific pathophysiology

Nature Biomedical Engineering(2020)10.1038/s41551-019-0495-z

N/A

0DataRank · unranked

298 citations

Viktoras Frismantas, Yuka Milton, Rhiannon David, Petar Pop-Damkov, Douglas Ferguson +24 more

Mitochondrial DNA variant detection in over 6,500 rare disease families by the systematic analysis of exome and genome sequencing data resolves undiagnosed cases

Human Genetics and Genomics Advances(2025)10.1016/j.xhgg.2025.100441

N/A

0DataRank · unranked

1 citations

Kristen M. Laricchia, Nicole J. Lake, Sushma Chaluvadi, Vijay Ganesh, Stephanie DiTroia +31 more

MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia

Cell stem cell(2020)10.1016/j.stem.2020.09.004

N/A

0DataRank · unranked

65 citations

Kaiyang Zhang, Anniina Färkkilä, Jessica Filiatrault, Chunyu Yang, Martha Velázquez +20 more

Inhibition of TGFβ1 and TGFβ3 promotes hematopoiesis in Fanconi anemia

Experimental Hematology(2020)10.1016/j.exphem.2020.11.002

N/A

0DataRank · unranked

23 citations

Chunyu Yang, Elissa Furutani, Benilde García‐de Teresa, Martha Velázquez, Jessica Filiatrault +16 more

A study assessing the feasibility of randomization of pediatric and young adult patients between matched unrelated donor bone marrow transplantation and immune‐suppressive therapy for newly diagnosed severe aplastic anemia: A joint pilot trial of the North American Pediatric Aplastic Anemia Consortium and the Pediatric Transplantation and Cellular Therapy Consortium

Pediatric Blood & Cancer(2020)10.1002/pbc.28444

N/A

0DataRank · unranked

25 citations

Leslie Lehmann, Alison A. Bertuch, Ghadir Sasa, Timothy S. Olson, Taizo A. Nakano +13 more

Distinct genetic pathways define pre-malignant versus compensatory clonal hematopoiesis in Shwachman-Diamond syndrome

Nature Communications(2021)10.1038/s41467-021-21588-4

N/A

0DataRank · unranked

180 citations

Kasiani C. Myers, James R. Bowman, Christopher J. Gibson, Nicholas D. Camarda, Elissa Furutani +38 more

Congenital X‐linked neutropenia with myelodysplasia and somatic tetraploidy due to a germline mutation in SEPT6

American Journal of Hematology(2021)10.1002/ajh.26382

N/A

0DataRank · unranked

8 citations

Katelyn E. Gagne, Ellen M. Beauchamp, Jonathan Fogel, Aleksej Perlov, Mireia Sola +17 more

Akiko Shimamura

Indexed papers

Top data-sharing exemplar

Papers