Stephan Sanders

University of California, San Francisco

Biochemistry, Genetics and Molecular Biology

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 1%percentile

5.7Author 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.

Frequency and Complexity of De Novo Structural Mutation in Autism

The American Journal of Human Genetics(2016)10.1016/j.ajhg.2016.02.018

Top 6%

3.6DataRank

Top 6%112 citations

Danny Antaki, Madhusudan Gujral, Amina Noor, Gabriel Rosanio, Timothy R. Chapman +34 more

Papers

Driven by 40 papers — median percentile 89. Top paper: “Frequency and Complexity of De Novo Structural Mutation in Autism”.

Frequency and Complexity of De Novo Structural Mutation in Autism

The American Journal of Human Genetics(2016)10.1016/j.ajhg.2016.02.018

Top 6%

3.6DataRank

Top 6%112 citations

Danny Antaki, Madhusudan Gujral, Amina Noor, Gabriel Rosanio, Timothy R. Chapman +34 more

Leveraging electronic health records and knowledge networks for Alzheimer’s disease prediction and sex-specific biological insights

Nature Aging(2024)10.1038/s43587-024-00573-8

N/A

2.1DataRank · unranked

76 citations

Katherine P. Rankin, Gabriel Cerono, Silvia Miramontes, Hunter Mills, Jacquelyn Roger +16 more

A Chromatin Accessibility Atlas of the Developing Human Telencephalon

Cell(2020)10.1016/j.cell.2020.06.002

Top 11%

2.0DataRank

Top 11%108 citations

Sean Whalen, Pawel F. Przytycki, Reuben Thomas, Fadya Binyameen, Tomasz J. Nowakowski +6 more

Single-cell multi-cohort dissection of the schizophrenia transcriptome

Science(2024)10.1126/science.adg5136

N/A

1.3DataRank · unranked

125 citations

Shahin Mohammadi, José Dávila-Velderrain, Sivan Subburaju, Daniel Reed Tso, Makayla Hourihan +196 more

Massively parallel characterization of regulatory elements in the developing human cortex

Science(2024)10.1126/science.adh0559

N/A

1.2DataRank · unranked

61 citations

Sean Whalen, Marilyn Steyert, Ryan Ziffra, Pawel F. Przytycki, Fumitaka Inoue +197 more

A framework for the interpretation of de novo mutation in human disease

Nature Genetics(2014)10.1038/ng.3050

N/A

1.1DataRank · unranked

1119 citations

Elise B Robinson, Stephan J. Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath +25 more

De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.02.012

N/A

0.722DataRank · unranked

122 citations

Harrison Brand, Harold Wang, Xuefang Zhao, Brent S. Pedersen, Julie Feusier +10 more

CRISPR activation for SCN2A-related neurodevelopmental disorders

Nature(2025)10.1038/s41586-025-09522-w

N/A

0.605DataRank · unranked

17 citations

Andrew D. Nelson, Perry W.E. Spratt, Elizabeth C. Hamada, Xujia Zhou, Henry Kyoung +23 more

Thalamocortical organoids enable in vitro modeling of 22q11.2 microdeletion associated with neuropsychiatric disorders

Cell stem cell(2024)10.1016/j.stem.2024.01.010

N/A

0.571DataRank · unranked

44 citations

Chang N. Kim, Jayden Ross, Kelsey M. Hennick, Sih‐Rong Wu, Neha Paranjape +22 more

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

10.1101/2021.12.20.21267194

N/A

0.538DataRank · unranked

35 citations

F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong +60 more

Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.12.248526

N/A

0.385DataRank · unranked

12 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry

Nature Human Behaviour(2025)10.1038/s41562-025-02145-1

N/A

0.345DataRank · unranked

9 citations

Anja Hollowell, Emilie M. Wigdor, M. MORGAN, Laurie J. Hannigan, Elizabeth C. Corfield +23 more

A Biomedical Open Knowledge Network Harnesses the Power of AI to Understand Deep Human Biology

AI Magazine(2022)10.1609/aimag.v43i1.19125

N/A

0.345DataRank · unranked

9 citations

Katy Börner, John P. Morris, Charlotte A. Nelson, Karthik Soman, Erica Schleimer +15 more

A biomedical open knowledge network harnesses the power of AI to understand deep human biology

AI Magazine(2022)10.1002/aaai.12037

N/A

0.330DataRank · unranked

8 citations

Katy Börner, John P. Morris, Charlotte A. Nelson, Karthik Soman, Erica Schleimer +15 more

Leveraging Electronic Medical Records and Knowledge Networks to Predict Disease Onset and Gain Biological Insight Into Alzheimer’s Disease

medRxiv(2023)10.1101/2023.03.14.23287224

N/A

0.306DataRank · unranked

5 citations

Katherine P. Rankin, Gabriel Cerono, Silvia Miramontes, Hunter Mills, Jacquelyn Roger +15 more

Nr2f1 enhancers have distinct functions in controlling Nr2f1 expression during cortical development

Proceedings of the National Academy of Sciences(2024)10.1073/pnas.2402368121

N/A

0.165DataRank · unranked

2 citations

Athéna R. Ypsilanti, Eirene Markenscoff-Papadimitriou, Diane E. Dickel, Stephan Sanders, Shan Dong +4 more

Molecular dynamics of Brodmann Area 22 in development and autism

10.64898/2026.03.31.715694

Top 70%

0.165DataRank

Top 70%2 citations

Emilie M. Wigdor, Yuhan Hao, Rachel Leonard, Joseph Asfouri, Michael Griffiths +14 more

Prevalence of Returnable Genetic Results Based on Recognizable Phenotypes among Children with Autism Spectrum Disorder

medRxiv(2021)10.1101/2021.05.28.21257736

N/A

0DataRank · unranked

2 citations

Audrey Thurm, Elise Robinson, Stephan Sanders, Somer Bishop

High-throughput characterization of the role of non-B DNA motifs on promoter function

Cell Genomics(2022)10.1016/j.xgen.2022.100111

N/A

0DataRank · unranked

62 citations

Jesús Victorino, Guillermo E. Parada, Vikram Agarwal, Jingjing Zhao, Hei Yuen Wong +10 more

Physical and functional convergence of the autism risk genes Scn2a and Ank2 in neocortical pyramidal cell dendrites

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.05.31.494205

N/A

0DataRank · unranked

4 citations

Amanda M. Catalfio, Julie M. Gupta, Lia Min, René N. Caballero-Florán, Kendall P. Dean +8 more

Systematic evaluation of genome sequencing for the diagnostic assessment of autism spectrum disorder and fetal structural anomalies

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.07.010

N/A

0DataRank · unranked

54 citations

Elise Valkanas, Jessica L. Giordano, Harold Z. Wang, Benjamin B Currall, Kathryn O’Keefe +40 more

Astrocytic β-catenin signaling via TCF7L2 regulates synapse development and social behavior

Molecular Psychiatry(2023)10.1038/s41380-023-02281-y

N/A

0DataRank · unranked

42 citations

Marcin Andrzej Lipiec, Ewa Liszewska, Ksenia Meyza, Joanna Urban‐Ciećko, Ludwika Kondrakiewicz +13 more

KCNT2‐Related Disorders: Phenotypes, Functional, and Pharmacological Properties

Annals of Neurology(2023)10.1002/ana.26662

N/A

0DataRank · unranked

21 citations

Ilaria Mosca, Paolo Ambrosino, Deborah Puzo, Allan Bayat, Saskia B. Wortmann +21 more

Paradoxical hyperexcitability from NaV1.2 sodium channel loss in neocortical pyramidal cells

Cell Reports(2021)10.1016/j.celrep.2021.109483

N/A

0DataRank · unranked

119 citations

Ryan P.D. Alexander, Roy Ben‐Shalom, Atehsa Sahagun, Henry Kyoung, Caroline M. Keeshen +3 more

Systematic identification of disease-causing promoter and untranslated region variants in 8,040 undiagnosed individuals with rare disease

medRxiv(2023)10.1101/2023.09.12.23295416

N/A

0DataRank · unranked

6 citations

Alexander J. M. Blakes, Ruebena Dawes, Scott D. Findlay, Jenny Lord, Susan Walker +17 more

Developmental dynamics of voltage-gated sodium channel isoform expression in the human and mouse neocortex

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.11.18.389171

N/A

0DataRank · unranked

2 citations

Siavash Fazel Darbandi, Sirisha Pochareddy, Forrest O. Gulden, Michael C. Gilson, Brooke Sheppard +8 more

Physical and functional convergence of the autism risk genes Scn2a and Ank2 in neocortical pyramidal cell dendrites

Neuron(2024)10.1016/j.neuron.2024.01.003

N/A

0DataRank · unranked

51 citations

Amanda M. Catalfio, Julie P. Gupta, Lia Min, René N. Caballero-Florán, Kendall P. Dean +8 more

Coordinated Interaction: A model and test for globally signed epistasis in complex traits

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.02.14.949883

N/A

0DataRank · unranked

3 citations

Nadav Rappoport, Po‐Ru Loh, Stephan Sanders, Andy Dahl, Noah Zaitlen +1 more

LARP1 haploinsufficiency is associated with an autosomal dominant neurodevelopmental disorder

Human Genetics and Genomics Advances(2024)10.1016/j.xhgg.2024.100345

N/A

0DataRank · unranked

6 citations

Raymond J. Louie, Olivia Larner, Robert G. Best, Kevin Chen, Josephine Morris +27 more

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv(2024)10.1101/2024.04.07.24305438

N/A

0DataRank · unranked

10 citations

Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton, Susan Walker, Alicia Ljungdahl +92 more

De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.10.06.329011

N/A

0DataRank · unranked

5 citations

Harrison Brand, Harold Wang, Xuefang Zhao, Brent S. Pedersen, Julie Feusier +9 more

Biallelic variants in the non-coding RNA gene RNU4-2 cause a recessive neurodevelopmental syndrome with distinct white matter changes

medRxiv(2025)10.1101/2025.08.13.25333306

N/A

0DataRank · unranked

5 citations

Alexander J. M. Blakes, Yuyang Chen, Joachim De Jonghe, Javeria Raza Alvi, Florence Amblard +69 more

A Retinoic Acid Autoregulatory Loop Governing Prefrontal-Motor Arealization

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.64898/2025.12.23.696038

N/A

0DataRank · unranked

1 citations

Mikihito Shibata, Saejeong Park, Yuting Liu, Iva Salamon, Jia Liu +13 more

Characterization of De Novo Promoter Variants in Autism Spectrum Disorder with Massively Parallel Reporter Assays

International Journal of Molecular Sciences(2023)10.3390/ijms24043509

N/A

0DataRank · unranked

16 citations

Joon‐Yong An, Fumitaka Inoue, Ajuni Sohota, Nadav Ahituv, Stephan Sanders +2 more

A model and test for coordinated polygenic epistasis in complex traits

Proceedings of the National Academy of Sciences(2021)10.1073/pnas.1922305118

N/A

0DataRank · unranked

34 citations

Nadav Rappoport, Po‐Ru Loh, Stephan Sanders, Noah Zaitlen, Andy Dahl +1 more

Patterns of delay in early gross motor and expressive language milestone attainment in probands with genetic conditions versus idiopathic ASD from SFARI registries

Journal of Child Psychology and Psychiatry(2021)10.1111/jcpp.13492

N/A

0DataRank · unranked

31 citations

Cristan Farmer, LeeAnne Green Snyder, Andrew R. Mitz, Stephan Sanders, Somer Bishop +2 more

Harnessing rare variants in neuropsychiatric and neurodevelopment disorders—a Keystone Symposia report

Annals of the New York Academy of Sciences(2021)10.1111/nyas.14658

N/A

0DataRank · unranked

7 citations

Ryan H. Purcell, Elise Robinson, Jacob Vorstman, Wendy K. Chung, John N. Constantino +9 more

Exome sequencing of fetuses with congenital diaphragmatic hernia supports a causal role for NR2F2, PTPN11, and WT1 variants

The American Journal of Surgery(2021)10.1016/j.amjsurg.2021.07.016

N/A

0DataRank · unranked

10 citations

Shan Dong, Billie R. Lianoglou, Alessandra F. Aguilar Lucero, Grace Schwartz, Mary E. Norton +3 more

Paradoxical hyperexcitability from Na V 1.2 sodium channel loss in neocortical pyramidal cells

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.02.02.429423

N/A

0DataRank · unranked

7 citations

Roy Ben‐Shalom, Atehsa Sahagun, Caroline M. Keeshen, Stephan Sanders, Kevin J. Bender +1 more

A Cre-dependent massively parallel reporter assay allows for cell-type specific assessment of the functional effects of non-coding elements in vivo

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.05.17.444514

N/A

0DataRank · unranked

6 citations

Stephen P. Plassmeyer, Anthony D. Fischer, Ryan Z. Friedman, Michael A. Rieger, Din Selmanovic +7 more

Stephan Sanders

Indexed papers

Top data-sharing exemplar

Papers