Sameer S. Bajikar

Also affiliated with Neurological Research Institute, Texas Children's Hospital

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 11 papers. Top paper: “Parameterizing cell-to-cell regulatory heterogeneities via stochastic transcriptional profiles”.

Parameterizing cell-to-cell regulatory heterogeneities via stochastic transcriptional profiles

Proceedings of the National Academy of Sciences(2014)10.1073/pnas.1311647111

N/A

1.1DataRank · unranked

57 citations

Christiane Fuchs, Andreas Roller, Fabian Joachim Theis, Kevin A. Janes, Sameer S. Bajikar

Disruption of MeCP2–TCF20 complex underlies distinct neurodevelopmental disorders

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2119078119

N/A

0.568DataRank · unranked

43 citations

Hamdan Hamdan, Hari Krishna Yalamanchili, Kaifang Pang, Amy E. Pohodich, Joanna Lopez +19 more

MeCP2 regulates Gdf11, a dosage-sensitive gene critical for neurological function

eLife(2023)10.7554/elife.83806

N/A

0.546DataRank · unranked

14 citations

Ashley G. Anderson, Jian Zhou, Mark A. Durham, Alexander J. Trostle, Ying‐Wooi Wan +3 more

Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

Genetics in Medicine(2021)10.1038/s41436-021-01216-8

N/A

0.494DataRank · unranked

26 citations

Jennifer B. Phillips, Elizabeth L. Fieg, Sameer S. Bajikar, Judy Peirce, Jeremy Wegner +94 more

Structural variant allelic heterogeneity in MECP2 duplication syndrome provides insight into clinical severity and variability of disease expression

Genome Medicine(2024)10.1186/s13073-024-01411-7

N/A

0.474DataRank · unranked

17 citations

Jesse D. Bengtsson, Sameer S. Bajikar, Christopher M. Grochowski, Ming Yin Lun, Mira Gandhi +38 more

Modeling antisense oligonucleotide therapy in MECP2 duplication syndrome human iPSC-derived neurons reveals gene expression programs responsive to MeCP2 levels

Human Molecular Genetics(2024)10.1093/hmg/ddae135

N/A

0.383DataRank · unranked

10 citations

Yehezkel Sztainberg, Alexander J. Trostle, Harini P Tirumala, Ying‐Wooi Wan, Caroline L Harrop +10 more

MeCP2 regulates Gdf11, a dosage-sensitive gene critical for neurological function

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.10.05.510925

N/A

0DataRank · unranked

0 citations

Ashley G. Anderson, Jian Zhou, Mark A. Durham, Alexander J. Trostle, Ying‐Wooi Wan +3 more

A novel pathogenic mutation of MeCP2 impairs chromatin association independent of protein levels

Genes & Development(2023)10.1101/gad.350733.123

N/A

0DataRank · unranked

16 citations

Claudia Cattoglio, Yingyao Shao, Harini P Tirumala, Carlo Vetralla, Sameer S. Bajikar +19 more

Acute MeCP2 loss in adult mice reveals transcriptional and chromatin changes that precede neurological dysfunction and inform pathogenesis

Neuron(2024)10.1016/j.neuron.2024.11.006

N/A

0DataRank · unranked

26 citations

Jian Zhou, Ryan O’Hara, Harini P Tirumala, Mark A. Durham, Alexander J. Trostle +10 more

Identification and characterization of conserved noncoding cis-regulatory elements that impact Mecp2 expression and neurological functions

Genes & Development(2021)10.1101/gad.345397.120

N/A

0DataRank · unranked

17 citations

Sameer S. Bajikar, Harini P Tirumala, Manuel Cantu Gutierrez, Joshua D. Wythe, Huda Y. Zoghbi +1 more

Antisense oligonucleotide therapy in a humanized mouse model of MECP2 duplication syndrome

Science Translational Medicine(2021)10.1126/scitranslmed.aaz7785

N/A

0DataRank · unranked

60 citations

Yehezkel Sztainberg, Qi Wang, Sameer S. Bajikar, Alexander J. Trostle, Ying‐Wooi Wan +6 more