Annapurna Poduri

Also affiliated with Boston Children's Hospital, National Institutes of Health, Harvard University, National Institute of Neurological Disorders and Stroke, Boston Children's Museum, Epilepsy Foundation, Massachusetts Institute of Technology

MedicineBiochemistry, Genetics and Molecular BiologyNeuroscience

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 2%percentile

2.9Author DataRank

Indexed papers

3in 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 3 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.

Assessing the landscape of STXBP1-related disorders in 534 individuals

Brain(2021)10.1093/brain/awab327

Top 9%

2.3DataRank

Top 9%125 citations

Shridhar Parthasarathy, Sarah M. Ruggiero, Ganna Balagura, Eryn Fitch, Katherine L. Helbig +48 more

Papers

Driven by 42 papers — median percentile 52. Top paper: “Assessing the landscape of STXBP1-related disorders in 534 individuals”.

Assessing the landscape of STXBP1-related disorders in 534 individuals

Brain(2021)10.1093/brain/awab327

Top 9%

2.3DataRank

Top 9%125 citations

Shridhar Parthasarathy, Sarah M. Ruggiero, Ganna Balagura, Eryn Fitch, Katherine L. Helbig +48 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

Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age

Advanced Genetics(2022)10.1002/ggn2.202200012

Top 57%

0.281DataRank

Top 57%4 citations

Élise Douard, Robin L. Haynes, Hyun Yong Koh, Alireza Haghighi, Christine Keywan +10 more

De novo missense variants in HDAC3 leading to epigenetic machinery dysfunction are associated with a variable neurodevelopmental disorder

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.06.015

N/A

0.269DataRank · unranked

5 citations

Seong-Kyun Lim, Hoseok Seo, Seungbok Lee, Jaeso Cho, Soo Yeon Kim +13 more

A de novo BRPF1 variant in a case of Sudden Unexplained Death in Childhood

European Journal of Medical Genetics(2020)10.1016/j.ejmg.2020.104002

N/A

0DataRank · unranked

19 citations

Ingrid A. Holm, Annapurna Poduri, Catherine A. Brownstein, Sanda Alexandrescu, Jennifer Chen +3 more

Epilepsy Benchmarks Area III: Improved Treatment Options for Controlling Seizures and Epilepsy-Related Conditions Without Side Effects

Epiliepsy currents/Epilepsy currents(2020)10.1177/1535759719895279

N/A

0DataRank · unranked

19 citations

Dennis Dlugos, David C. Henshall, Heather C. Mefford, Michael A. Rogawski, Kevin J. Staley +4 more

Epilepsy Benchmarks Area IV: Limit or Prevent Adverse Consequence of Seizures and Their Treatment Across the Life Span

Epiliepsy currents/Epilepsy currents(2020)10.1177/1535759719895277

N/A

0DataRank · unranked

13 citations

Miya R. Asato, Mesha‐Gay Brown, Julia Doss, Elizabeth A. Felton, Jennifer A. Kearney +5 more

Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.08.003

N/A

0DataRank · unranked

46 citations

Shiva Ganesan, David Lewis‐Smith, Sarah McKeown, Manuela Pendziwiat, Katherine L. Helbig +13 more

Current neurologic treatment and emerging therapies in CDKL5 deficiency disorder

Journal of Neurodevelopmental Disorders(2021)10.1186/s11689-021-09384-z

N/A

0DataRank · unranked

48 citations

Carolyn I. Daniels, Isabel Haviland, Lindsay C. Swanson, Caitlin Greene, Anne Marie M. Denny +14 more

Uridine‐responsive epileptic encephalopathy due to inherited variants in CAD: A Tale of Two Siblings

Annals of Clinical and Translational Neurology(2021)10.1002/acn3.51272

N/A

0DataRank · unranked

17 citations

Sonal Mahida, Parul Jayakar, Hyun Yong Koh, Alan Taylor, Trevor Resnick +7 more

Somatic mutation involving diverse genes leads to a spectrum of focal cortical malformations

medRxiv(2021)10.1101/2021.12.22.21267563

N/A

0DataRank · unranked

4 citations

Meethila Gade, Edward Yang, Hyun Yong Koh, Nicole M. Walley, Anne F. Buckley +18 more

Mosaic and non-mosaic protocadherin 19 mutation leads to neuronal hyperexcitability in zebrafish

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.09.03.458732

N/A

0DataRank · unranked

1 citations

Xinzhu Yang, Christopher M. McGraw, Laura Turner, Carsten Robens, Summer B. Thyme +3 more

Mendelian etiologies identified with whole exome sequencing in cerebral palsy

Annals of Clinical and Translational Neurology(2022)10.1002/acn3.51506

N/A

0DataRank · unranked

82 citations

Dustin L. Gable, Jamie Love‐Nichols, Alexa Tsao, Shira Rockowitz, Piotr Sliz +34 more

Somatic variants in diverse genes leads to a spectrum of focal cortical malformations

Brain(2022)10.1093/brain/awac117

N/A

0DataRank · unranked

78 citations

Meethila Gade, Edward Yang, Hyun Yong Koh, Jinfeng Lü, Nicole M Walley +20 more

Clinical Features, Neuropathology, and Surgical Outcome in Patients With Refractory Epilepsy and Brain Somatic Variants in the SLC35A2 Gene

Neurology(2022)10.1212/wnl.0000000000201471

N/A

0DataRank · unranked

55 citations

Ingmar Blümcke, Melodie R. Winawer, Till Hartlieb, Hoon‐Chul Kang, Laura Grisotto +31 more

Clinical, biochemical and genetic characteristics of MOGS-CDG: a rare congenital disorder of glycosylation

Journal of Medical Genetics(2022)10.1136/jmedgenet-2021-108177

N/A

0DataRank · unranked

21 citations

Bobby G. Ng, Amy White, Kim K. Nickander, Coleman Turgeon, Kristen Liedtke +31 more

PIGNencephalopathy: Characterizing the epileptology

Epilepsia(2022)10.1111/epi.17173

N/A

0DataRank · unranked

8 citations

Guillem de Valles‐Ibáñez, Manuela Pendziwiat, Alexej Knaus, Kerstin Alt, Elisa Biamino +64 more

Somatic Ras/Raf/MAPK Variants Enriched in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy

medRxiv(2022)10.1101/2022.12.23.22283854

N/A

0DataRank · unranked

5 citations

Yilan Wang, Yasmine Chahine, E. Zeynep Erson‐Omay, Stephanie M. Robert, Emre Kiziltug +36 more

Brain somatic mosaicism in epilepsy: Bringing results back to the clinic

Neurobiology of Disease(2023)10.1016/j.nbd.2023.106104

N/A

0DataRank · unranked

35 citations

Annapurna Poduri, Alissa M. D’Gama

Post-zygotic rescue of meiotic errors causes brain mosaicism and focal epilepsy

Nature Genetics(2023)10.1038/s41588-023-01547-z

N/A

0DataRank · unranked

25 citations

Adithe Rivaldi, Noriyuki Shinagawa, Sahibjot Sran, Jason B. Navarro, Jesse J. Westfall +29 more

Clinical and functional consequences of GRIA variants in patients with neurological diseases

Cellular and Molecular Life Sciences(2023)10.1007/s00018-023-04991-6

N/A

0DataRank · unranked

19 citations

Riley E. Perszyk, Nana Liu, Yuchen Xu, Subhrajit Bhattacharya, Gil Shaulsky +25 more

Toward representative genomic research: the children’s rare disease cohorts experience

Therapeutic Advances in Rare Disease(2023)10.1177/26330040231181406

N/A

0DataRank · unranked

17 citations

Eurnestine Brown, Shira Rockowitz, Ted Lee, Bo Zhang, Abigail Sveden +6 more

Epileptic spasms in CDKL5 deficiency disorder: Delayed treatment and poor response to first‐line therapies

Epilepsia(2023)10.1111/epi.17630

N/A

0DataRank · unranked

11 citations

Scott Demarest, Elia Pestana‐Knight, Ahsan N. Moosa, Xiaoming Zhang, José R. Pérez‐Pérez +17 more

Zebrafish models of candidate human epilepsy-associated genes provide evidence of hyperexcitability

iScience(2024)10.1016/j.isci.2024.110172

N/A

0DataRank · unranked

17 citations

Jeremy F.P. Ullmann, Hyun Yong Koh, Laura Turner, Cristina M. Baker, Barbara K. Robens +5 more

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2023.12.004

N/A

0DataRank · unranked

14 citations

Sydney L. Michener, Hongling Pan, Hiuling Chan, Jessica M. Pfliger, Jill A. Rosenfeld +95 more

Clinical utility of a genetic diagnosis in individuals with cerebral palsy and related motor disorders

Annals of Clinical and Translational Neurology(2024)10.1002/acn3.51942

N/A

0DataRank · unranked

9 citations

Dustin L. Gable, Zoë Frazier, Abigail Sveden, Aisling Quinlan, Maya Chopra +5 more

Cerebral Palsy Phenotypes in Genetic Epilepsies

Pediatric Neurology(2024)10.1016/j.pediatrneurol.2024.05.016

N/A

0DataRank · unranked

1 citations

Hyun Yong Koh, Lacey Smith, Annapurna Poduri, Christelle Moufawad El Achkar, Ann Bergin +13 more

Zebrafish models of candidate human epilepsy-associated genes provide evidence of hyperexcitability

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.02.07.579190

N/A

0DataRank · unranked

5 citations

Jeremy F.P. Ullmann, Hyun Yong Koh, Laura Turner, Cristina M. Baker, Barbara K. Robens +5 more

Analysis of DNA from brain tissue on stereo-EEG electrodes reveals mosaic epilepsy-related variants

medRxiv(2024)10.1101/2024.07.21.24310779

N/A

0DataRank · unranked

1 citations

H. Westley Phillips, Yilan Wang, Michelle Chiu, Yasmine Chahine, Amanda Cantu Swanson +12 more

Machine learning enables high-throughput, low-replicate screening for novel anti-seizure targets and compounds using combined movement and calcium fluorescence in larval zebrafish

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.08.01.606228

N/A

0DataRank · unranked

1 citations

Annapurna Poduri, Christopher M. McGraw

Post-zygotic rescue of meiotic errors causes brain mosaicism and focal epilepsy

UNC Libraries(2024)10.17615/8wx3-1a14

N/A

0DataRank · unranked

0 citations

Katherine E. Miller, Diana Thomas, Christopher R. Pierson, Gretchen K. Von Allmen, Edward Yang +29 more

Somatic variants in diverse genes leads to a spectrum of focal cortical malformations

UNC Libraries(2024)10.17615/98hm-r135

N/A

0DataRank · unranked

0 citations

Peter Canoll, Anne F. Buckley, Gretchen K. Von Allmen, Hyun Yong Koh, Gerald A. Grant +20 more

Cell-type-informed genotyping of mosaic focal epilepsies reveals cell-autonomous and non-cell-autonomous disease-associated transcriptional programs

Proceedings of the National Academy of Sciences(2025)10.1073/pnas.2509622122

N/A

0DataRank · unranked

13 citations

Maya Talukdar, Edward Stronge, Rosita B. Ramirez, Yingxi Yang, August Yue Huang +20 more

Machine learning enables high-throughput, low-replicate screening for novel anti-seizure targets and compounds using combined movement and calcium fluorescence in larval zebrafish

European Journal of Pharmacology(2025)10.1016/j.ejphar.2025.177327

N/A

0DataRank · unranked

6 citations

Annapurna Poduri, Christopher M. McGraw

Characterization of the functional and clinical impacts of CACNA1A missense variants found in neurodevelopmental disorders

Science Translational Medicine(2025)10.1126/scitranslmed.adr0024

N/A

0DataRank · unranked

3 citations

Lei Cui, Nikita Budnik, Siwei Chen, Erick Olivares, David Báez-Nieto +14 more

Sequence variants in HECTD1 result in a variable neurodevelopmental disorder

The American Journal of Human Genetics(2025)10.1016/j.ajhg.2025.01.001

N/A

0DataRank · unranked

4 citations

Elias Oxman, Hieu D. Hoang, Wu‐Lin Charng, Tanvitha Kotla, Weimin Yuan +49 more

The Use of Synaptic Extracellular Myo‐Inositol to Treat Developmental and Epileptic Encephalopathy

Annals of the Child Neurology Society(2025)10.1002/cns3.70029

N/A

0DataRank · unranked

1 citations

Didem Demirbas, Lance H. Rodan, Edward Yang, Sanjay P. Prabhu, Jie Chen +11 more

De novo HDAC3 variants leading to epigenetic machinery dysfunction are associated with a neurodevelopmental disorder

medRxiv(2024)10.1101/2024.01.29.24301801

N/A

0DataRank · unranked

0 citations

Seong-Kyun Lim, Hoseok Seo, Seungbok Lee, Jaeso Cho, Soo Yeon Kim +10 more

Characterization of the functional and clinical impacts of CACNA1A missense variants found in neurodevelopmental disorders

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.04.23.650298

N/A

0DataRank · unranked

0 citations

Lei Cui, Nikita Budnik, Siwei Chen, Erick Olivares, David Báez-Nieto +11 more

Modelling and treating GRIN2A developmental and epileptic encephalopathy in mice

Brain(2020)10.1093/brain/awaa147

N/A

0DataRank · unranked

83 citations

Christopher D. Bostick, Heather E. Olson, Jurrian Peters, Chad R. Camp, Daniel Krizay +21 more

Children’s rare disease cohorts: an integrative research and clinical genomics initiative

npj Genomic Medicine(2020)10.1038/s41525-020-0137-0

N/A

0DataRank · unranked

68 citations

Nicholas LeCompte, Mary M. Carmack, Andrew Quitadamo, Lily Wang, Meredith Park +16 more

Mortality in infantile spasms: A hospital‐based study

Epilepsia(2020)10.1111/epi.16468

N/A

0DataRank · unranked

41 citations

Elanagan Nagarajan, Ann M. Bergin, Phillip L. Pearl, Tobias Loddenkemper, Masanori Takeoka +9 more

Annapurna Poduri

Indexed papers

Top data-sharing exemplar

Papers