Sharmila Banerjee‐Basu

3.9k citations

36 papers · 2.6k indexed · 1 hit paper · h-index 21

Co-authors: Alan Packer Andreas D. Baxevanis Idan Menashe Andrés Buonanno Lauren A. Weiss Heather C. Mefford Eric M. Morrow Brett S. Abrahams
Topics: Autism Spectrum Disorder Research (13 papers)Genetics and Neurodevelopmental Disorders (12 papers)RNA and protein synthesis mechanisms (6 papers)
Cited by: Cognitive Neuroscience Genetics Molecular Biology
Journals: Nucleic Acids Research Nature Genetics PLoS ONE
Partner nations: United States Israel United Kingdom

In The Last Decade

Sharmila Banerjee‐Basu

36 papers receiving 2.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)

2013 495 citations Brett S. Abrahams, Dan E. Arking et al. Molecular Autism profile →

Peers

Countries citing papers authored by Sharmila Banerjee‐Basu

Since Specialization

Citations

This map shows the geographic impact of Sharmila Banerjee‐Basu's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sharmila Banerjee‐Basu with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sharmila Banerjee‐Basu more than expected).

Fields of papers citing papers by Sharmila Banerjee‐Basu

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sharmila Banerjee‐Basu. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sharmila Banerjee‐Basu. The network helps show where Sharmila Banerjee‐Basu may publish in the future.

Co-authorship network of co-authors of Sharmila Banerjee‐Basu

This figure shows the co-authorship network connecting the top 25 collaborators of Sharmila Banerjee‐Basu. A scholar is included among the top collaborators of Sharmila Banerjee‐Basu based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sharmila Banerjee‐Basu. Sharmila Banerjee‐Basu is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	A multifaceted approach for analyzing complex phenotypic data in rodent models of autism 2019 ·Molecular Autism ·(unknown),(unknown),(unknown),Sharmila Banerjee‐Basu	8
2	Common microRNAs Target Established ASD Genes 2014 ·Frontiers in Neurology ·Sharmila Banerjee‐Basu,Eric Larsen,Sabina Muend	14
3	STX1A and Asperger syndrome: a replication study 2014 ·Molecular Autism ·Jaroslava Durdiaková,Varun Warrier,Sharmila Banerjee‐Basu,Simon Baron‐Cohen,Bhismadev Chakrabarti	19
4	SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)breakdown → 2013 ·Molecular Autism ·Brett S. Abrahams,Dan E. Arking,Jerry L. Campbell,Heather C. Mefford,Eric M. Morrow,Lauren A. Weiss,Idan Menashe,(unknown),Sharmila Banerjee‐Basu,Alan Packer	495
5	Prioritization of Copy Number Variation Loci Associated with Autism from AutDB–An Integrative Multi-Study Genetic Database 2013 ·PLoS ONE ·Idan Menashe,Eric Larsen,Sharmila Banerjee‐Basu	25
6	Animal model integration to AutDB, a genetic database for autism 2011 ·BMC Medical Genomics ·(unknown),(unknown),Catherine Croft Swanwick,(unknown),(unknown),Sharmila Banerjee‐Basu	20
7	Loss-of-Function Mutations in Growth Differentiation Factor-1 (GDF1) Are Associated with Congenital Heart Defects in Humans 2007 ·The American Journal of Human Genetics ·Jayaprakash D. Karkera,(unknown),Erich Roessler,Sharmila Banerjee‐Basu,Maia V. Ouspenskaia,Jesse Mez,Elizabeth Goldmuntz,(unknown),Jeffrey A. Towbin,John W. Belmont,Andreas D. Baxevanis,Alexander F. Schier,Maximilian Muenke	82
8	The zebrafish gene claudinj is essential for normal ear function and important for the formation of the otoliths 2005 ·Mechanisms of Development ·(unknown),(unknown),Sharmila Banerjee‐Basu,Thomas Becker,Shawn M. Burgess	33
9	Structural analysis of disease‐causing mutations in the P‐subfamily of forkhead transcription factors 2004 ·Proteins Structure Function and Bioinformatics ·Sharmila Banerjee‐Basu,Andreas D. Baxevanis	15
10	The Homeodomain Resource: 2003 update 2003 ·Nucleic Acids Research ·Sharmila Banerjee‐Basu	16
11	The DNA-binding region of RAG 1 is not a homeodomain. 2002 ·Genome Biology ·Sharmila Banerjee‐Basu,Andreas D. Baxevanis	6
12	Molecular evolution of the homeodomain family of transcription factors 2001 ·Nucleic Acids Research ·Sharmila Banerjee‐Basu	135
13	Predictive Methods Using Protein Sequences 2001 ·Methods of biochemical analysis ·Sharmila Banerjee‐Basu,Andreas D. Baxevanis	2
14	The Homeodomain Resource: sequences, structures, DNA binding sites and genomic information 2001 ·Nucleic Acids Research ·Sharmila Banerjee‐Basu	20
15	MLH3: a DNA mismatch repair gene associated with mammalian microsatellite instability 2000 ·Nature Genetics ·Steven M. Lipkin,Victoria Wang,Russell F. Jacoby,Sharmila Banerjee‐Basu,Andreas D. Baxevanis,H. Lynch,(unknown),Francis S. Collins	248
16	The Homeodomain Resource: a prototype database for a large protein family 2000 ·Nucleic Acids Research ·Sharmila Banerjee‐Basu	11
17	Mutation of a gene encoding a putative chaperonin causes McKusick-Kaufman syndrome 2000 ·Nature Genetics ·Deborah L. Stone,Anne Slavotinek,Gerard G. Bouffard,Sharmila Banerjee‐Basu,Andreas D. Baxevanis,Mason Barr,Leslie G. Biesecker	143
18	Threading analysis of the Pitx2 homeodomain: Predicted structural effects of mutations causing Rieger syndrome and iridogoniodysgenesis 1999 ·Human Mutation ·Sharmila Banerjee‐Basu,Andreas D. Baxevanis	9
19	Chicken homeobox gene prox 1 related toDrosophila prospero is expressed in the developing lens and retina 1996 ·Developmental Dynamics ·Stanislav I. Tomarev,Olof Sundin,Sharmila Banerjee‐Basu,Melinda K. Duncan,(unknown),Joram Piatigorsky	107
20	Isolation and structure of the rat gene encoding troponin Islow 1994 ·Gene ·Sharmila Banerjee‐Basu,Andrés Buonanno	8

About Sharmila Banerjee‐Basu

Sharmila Banerjee‐Basu is a scholar working on Cognitive Neuroscience, Genetics and Aging, having authored 36 papers that have together received 2.6k indexed citations. Recurring topics across this work include Autism Spectrum Disorder Research (13 papers), Genetics and Neurodevelopmental Disorders (12 papers) and RNA and protein synthesis mechanisms (6 papers). The work is most often cited by research in Cognitive Neuroscience (820 citations), Genetics (1.2k citations) and Molecular Biology (1.6k citations). Sharmila Banerjee‐Basu has collaborated with scholars based in United States, Israel and United Kingdom. Frequent co-authors include Alan Packer, Andreas D. Baxevanis, Idan Menashe, Andrés Buonanno, Lauren A. Weiss, Heather C. Mefford, Eric M. Morrow, Brett S. Abrahams, Jerry L. Campbell and Dan E. Arking. Their work appears in journals such as Nucleic Acids Research, Nature Genetics and PLoS ONE.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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