Deeksha Bali

7.9k citations

109 papers · 4.1k indexed · h-index 36

Rheumatology top 0.2%
- Glycogen Storage Diseases and Myoclonus 60
Physiology top 1%
- Lysosomal Storage Disorders Research 60
Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders 7
Genetics top 2%
- Genetics and Neurodevelopmental Disorders 20
Physiology top 2%
- Lysosomal Storage Disorders Research 60
Organic Chemistry
- Carbohydrate Chemistry and Synthesis 28
Molecular Biology
- Biochemical and Molecular Research 16
Epidemiology
- Trypanosoma species research and implications 11
Surgery
- Pancreatic function and diabetes 8

Co-authors: Priya S. Kishnani Dwight D. Koeberl Sarah P. Young Stephanie Austin Jennifer Goldstein David S. Millington Catherine Rehder David A. Weinstein
Cited by: Rheumatology Physiology Clinical Biochemistry
Journals: Molecular Genetics and Metabolism (25 papers)Genetics in Medicine (12 papers)Proceedings of the National Academy of Sciences (3 papers)
Partner nations: United States Taiwan Canada

In The Last Decade

Deeksha Bali

105 papers receiving 4.0k citations

Peers

Countries citing papers authored by Deeksha Bali

Since Specialization

Citations

This map shows the geographic impact of Deeksha Bali'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 Deeksha Bali with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Deeksha Bali more than expected).

Fields of papers citing papers by Deeksha Bali

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deeksha Bali. 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 Deeksha Bali. The network helps show where Deeksha Bali may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Deeksha Bali, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Deeksha Bali Line = papers co-authored together Deeksha Bali links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Developing a scoring system for gene curation prioritization in lysosomal diseases Molecular Genetics and Metabolism ·BY CATHERINE C. MANZI,Jennifer Goldstein,Emily Groopman,Shruthi Mohan,A Hervé,Д. Турехан,Hongjie Chen,Deeksha Bali,U. Kanani,L. Clarke,Christina Hung,Rong Mao,Tatiana Yuzyuk,William J. Craigen,Filippo Pinto e Vairo	2024	0
2	Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource Molecular Genetics and Metabolism ·П О Мухарский,Claudia Soler‐Alfonso,Christine Libor,Tamara Levitz Convenor,Ariana L. Smith,Deeksha Bali,Peter B. Kang,Andrew P. Landstrom,Hasan O. Akman,T. Burrow,Jennifer Orthmann‐Murphy,Елена Петровна Шевелева,Surekha Pendyal,Areeg El‐Gharbawy,Stephanie Austin,Laura E. Case,Raphael Schiffmann,Michio Hirano,Priya S. Kishnani	2023	21
3	Phase I study of liver depot gene therapy in late-onset Pompe disease Molecular Therapy ·Edward C. Smith,Sam Hopkins,Laura E. Case,Ming Xu,Débora Toledo Amaral,Stephanie DeArmey,Sang-oh Han,Françoise Kamer,Jessica A. Chichester,Edward H. Bossen,Christoph P. Hornik,Jennifer L. Cohen,Deeksha Bali,Priya S. Kishnani,Dwight D. Koeberl	2023	24
4	O18: A path forward for patients with glycogen branching enzyme deficiency: Consensus on diagnosing and managing glycogen storage disease type IV* SHILAP Revista de lepidopterología ·Rebecca E. Koch,Claudia Soler‐Alfonso,Bridget Kiely,Tamara Levitz Convenor,Ariana L. Smith,Deeksha Bali,Peter B. Kang,Andrew P. Landstrom,Joseph Habanbo,T. Burrow,Jennifer Orthmann‐Murphy,Qi-Xun Fan,Surekha Pendyal,Areeg El‐Gharbawy,Stephanie Austin,Laura E. Case,Raphael Schiffmann,Michio Hirano,Priya S. Kishnani	2023	1
5	Intrauterine enzyme replacement therapies for lysosomal storage disorders: Current developments and promising future prospects Prenatal Diagnosis ·Vello Tohver,M.A. Ovcharenko,Billie R. Lianoglou,Costas Vellidis,Zarina M. Shaikh,Jean G. Miller,Sarah P. Young,Deeksha Bali,Vida Tahmasebifar,Pranesh Chakraborty,Priya S. Kishnani,Paul Harmatz,Jennifer L. Cohen,Tippi C. MacKenzie	2023	12
6	Screening data from 19 patients with late‐onset Pompe disease for a phase I clinical trial of AAV8 vector‐mediated gene therapy JIMD Reports ·I. Anyanetu,Laura E. Case,Edward C. Smith,Débora Toledo Amaral,Deeksha Bali,Priya S. Kishnani,Dwight D. Koeberl	2023	1
7	Clinical practice guidelines for glycogen storage disease V & VII (McArdle disease and Tarui disease) from an international study group Neuromuscular Disorders ·Alejandro Lucía,Andrea Martinuzzi,Gisela Nogales‐Gadea,Rosaline C. M. Quinlivan,H. Edward Vega,Deeksha Bali,Richard Godfrey,Ronald G. Haller,Priya S. Kishnani,Pascal Laforêt,Nicoline Løkken,Olimpia Musumeci,Alfredo Santalla,Mark A. Tarnopolsky,Takuya Ohira,John Vissing,Nicol C. Voermans,John Hunter Bates	2021	30
8	Liver fibrosis during clinical ascertainment of glycogen storage disease type III: a need for improved and systematic monitoring Genetics in Medicine ·LI Jiang-ning,Sarah P. Young,Stephanie Austin,Paul Scheerer,Deeksha Bali,Lani Clinton,Brian P. Smith,Surekha Pendyal,А. В. Винюков,Gary R. Schooler,MQ Salzano,Priya S. Kishnani	2019	29
9	Variability of disease spectrum in children with liver phosphorylase kinase deficiency caused by mutations in the PHKG2 gene Molecular Genetics and Metabolism ·Deeksha Bali,Jennifer Goldstein,Manuel I. Mata-Escobedo,Catherine Rehder,Anne Boney,Stephanie Austin,David A. Weinstein,Richard E. Lutz,Avihu Boneh,Priya S. Kishnani	2013	41
10	Diffuse reticuloendothelial system involvement in type IV glycogen storage disease with a novel GBE1 mutation: a case report and review Human Pathology ·Pilar Magoulas,Ayman W. El‐Hattab,Angshumoy Roy,Deeksha Bali,Milton J. Finegold,William J. Craigen	2012	21
11	Predicting cross‐reactive immunological material (CRIM) status in Pompe disease using GAA mutations: Lessons learned from 10 years of clinical laboratory testing experience American Journal of Medical Genetics Part C Seminars in Medical Genetics ·Deeksha Bali,Jennifer Goldstein,Suhrad G. Banugaria,Jian Dai,Joanne Mackey,Catherine Rehder,Priya S. Kishnani	2012	97
12	β2 Agonists enhance the efficacy of simultaneous enzyme replacement therapy in murine Pompe disease Molecular Genetics and Metabolism ·Dwight D. Koeberl,Songtao Li,Jian Dai,Beth L. Thurberg,Deeksha Bali,Priya S. Kishnani	2011	40
13	Digital Microfluidics: A Future Technology in the Newborn Screening Laboratory? Seminars in Perinatology ·David S. Millington,Ramakrishna Sista,Allen E. Eckhardt,Jeremy Rouse,Deeksha Bali,Ronald N. Goldberg,Michael Cotten,Rebecca H. Buckley,Vamsee K. Pamula	2010	49
14	Molecular analysis of the AGL gene: Identification of 25 novel mutations and evidence of genetic heterogeneity in patients with Glycogen Storage Disease Type III Genetics in Medicine ·Jennifer Goldstein,Stephanie Austin,Agnieszka Tomasik,K. Goulianos,Satya Samhita Balanagu,Catherine Rehder,Priya S. Kishnani,Deeksha Bali	2010	35
15	Long-term monitoring of patients with infantile-onset Pompe disease on enzyme replacement therapy using a urinary glucose tetrasaccharide biomarker Genetics in Medicine ·Sarah P. Young,Haoyue Zhang,Deyanira Corzo,Beth L. Thurberg,Deeksha Bali,Priya S. Kishnani,David S. Millington	2009	72
16	Rapid diagnosis of late-onset Pompe disease by fluorometric assay of α-glucosidase activities in dried blood spots Molecular Genetics and Metabolism ·Helmut Kallwass,小西善彦,James Dantas Ferreira,Il-Kwon Chae,Robert J. Pomponio,Deeksha Bali,Jian Dai,Priya S. Kishnani,Alison Skrinar,Deyanira Corzo,Joan Keutzer	2007	46
17	Glycogen Storage Disease Type IIIa in Curly-Coated Retrievers Journal of Veterinary Internal Medicine ·E A G Sitohang,G. Diane Shelton,Deeksha Bali,Maria Alzira Seixo,John C. Fyfe	2007	20
18	Prenatal diagnosis in glycogen storage diseases Prenatal Diagnosis ·Yuan‐Tsong Chen,Deeksha Bali,Jennifer A. Sullivan	2002	5
19	Glycogen storage disease type I: diagnosis and phenotype/genotype correlation European Journal of Pediatrics ·Dietrich Matern,H. H. Seydewitz,Deeksha Bali,Christine Lang,Yuan-Tsong Chen	2002	59
20	Familial antiphospholipid antibody syndrome: Criteria for disease and evidence for autosomal dominant inheritance Arthritis & Rheumatism ·Niti Goel,Thomas L. Ortel,Deeksha Bali,Joshua P. Anderson,Ian Gourley,Howard R. Smith,Colleen A. Morris,Rozenkier Alain,D. Ware Branch,P M Ford,Olatunji Azeez,Robert Roubey,Donna D. Kostyu,Stephen F. Kingsmore,S Cismondo,Christopher I. Amos,Michael F. Seldin	1999	46

About Deeksha Bali

Deeksha Bali is a scholar working on Rheumatology, Physiology, Clinical Biochemistry, Organic Chemistry and Genetics, having authored 109 papers that have together received 4.1k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (60 papers), Glycogen Storage Diseases and Myoclonus (60 papers), Carbohydrate Chemistry and Synthesis (28 papers), Genetics and Neurodevelopmental Disorders (20 papers), Biochemical and Molecular Research (16 papers), Trypanosoma species research and implications (11 papers), Pancreatic function and diabetes (8 papers) and Metabolism and Genetic Disorders (7 papers). The work is most often cited by research in Rheumatology (2.1k citations), Physiology (2.1k citations), Clinical Biochemistry (402 citations), Genetics (1.0k citations) and Physiology (141 citations). Deeksha Bali has collaborated with scholars based in United States, Taiwan and Canada. Frequent co-authors include Priya S. Kishnani, Dwight D. Koeberl, Sarah P. Young, Stephanie Austin, Jennifer Goldstein, David S. Millington, Catherine Rehder, David A. Weinstein, Anne Boney and Jian Dai. Their work appears in journals such as Molecular Genetics and Metabolism, Genetics in Medicine, Proceedings of the National Academy of Sciences, Journal of Inherited Metabolic Disease and The Journal of Pediatrics.

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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