Steven E. Boyden

Also affiliated with Center for Human Genetics, Baim Institute for Clinical Research, Star Center

Biochemistry, Genetics and Molecular BiologyMedicine

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 8 papers. Top paper: “Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations”.

Joint, multifaceted genomic analysis enables diagnosis of diverse, ultra-rare monogenic presentations

Nature Communications(2025)10.1038/s41467-025-61712-2

N/A

0.269DataRank · unranked

5 citations

Mikhail A. Moldovan, Rebecca Reimers, Daniel Traviglia, Xinyun Li, Danielle Barnum +95 more

Comprehensive variant calling from whole‐genome sequencing identifies a complex inversion that disrupts ZFPM2 in familial congenital diaphragmatic hernia

Molecular Genetics & Genomic Medicine(2022)10.1002/mgg3.1888

N/A

0DataRank · unranked

8 citations

Najla Al‐Sweel, Andrew Farrell, Rong Mao, Pınar Bayrak‐Toydemir, Christine E. Miller +22 more

Rapid genome sequencing identifies a novel de novoSNAP25variant for neonatal congenital myasthenic syndrome

Molecular Case Studies(2022)10.1101/mcs.a006242

N/A

0DataRank · unranked

15 citations

Ting Wen, Andrew Farrell, Rong Mao, Barry Moore, Steven E. Boyden +14 more

Novel molecular mechanism in Malan syndrome uncovered through genome sequencing reanalysis, exon‐level Array, and RNA sequencing

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63516

N/A

0DataRank · unranked

2 citations

Nicola Longo, Robert G. Lewis, Thomas J. Nicholas, Steven E. Boyden, Ashley Andrews +6 more

RNA sequencing provides functional insights and diagnostic resolution in previously unsolved rare disease cases

BMC Medical Genomics(2025)10.1186/s12920-025-02227-z

N/A

0DataRank · unranked

4 citations

John M. O’Shea, Lucilla Pizzo, Ting Wen, Makenzie Fulmer, Jian Zhao +20 more

Identification of 2 novel noncoding variants in patients with Diamond-Blackfan anemia syndrome by whole genome sequencing

Blood Advances(2025)10.1182/bloodadvances.2024015347

N/A

0DataRank · unranked

3 citations

Steven E. Boyden, Caleb M. Hocutt, Robert G. Lewis, Erin E. Baldwin, Jennie Vagher +9 more

Critical Signaling Events in the Mechanoactivation of Human Mast Cells through p.C492Y-ADGRE2

Journal of Investigative Dermatology(2020)10.1016/j.jid.2020.03.936

N/A

0DataRank · unranked

28 citations

Geethani Bandara, Yun Bai, Margery Smelkinson, Araceli Tobío, Hirsh D. Komarow +5 more

Worth the Effort: Lessons for Discovery and Care From an Unusual Case of Gorlin Syndrome

American Journal of Medical Genetics Part A(2025)10.1002/ajmg.a.64108

N/A

0DataRank · unranked

0 citations

Jian Zhao, Steven E. Boyden, Rong Mao, Pınar Bayrak‐Toydemir, A. Pflaum +9 more