D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Genetics D-index 67 Citations 25,485 193 World Ranking 1727 National Ranking 794

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Mutation
  • Genetics

Teepu Siddique focuses on Amyotrophic lateral sclerosis, Genetics, SOD1, Mutation and Genetic linkage. His work on TARDBP and UBQLN2 as part of general Amyotrophic lateral sclerosis research is frequently linked to RNA-Binding Protein FUS, thereby connecting diverse disciplines of science. His study explores the link between Genetics and topics such as Frontotemporal dementia that cross with problems in Penetrance and Haplotype.

His SOD1 research incorporates elements of Genetically modified mouse and Hyaline inclusion. His Mutation research incorporates themes from Internal medicine, Neurodegeneration, Endocrinology and Age of onset. He focuses mostly in the field of Genetic linkage, narrowing it down to topics relating to Chromosome 21 and, in certain cases, Linkage, Lod score, Paralysis, Pediatrics and Alzheimer's disease.

His most cited work include:

  • Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. (1871 citations)
  • Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase (1285 citations)
  • Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia (814 citations)

What are the main themes of his work throughout his whole career to date?

His primary scientific interests are in Amyotrophic lateral sclerosis, Genetics, SOD1, Neuroscience and Gene. His Amyotrophic lateral sclerosis study incorporates themes from Mutation and Neurodegeneration. His work deals with themes such as UBQLN2 and Protein degradation, which intersect with Mutation.

Locus, Genetic linkage, Gene mapping, Genetic marker and Genetic heterogeneity are the primary areas of interest in his Genetics study. His studies deal with areas such as Chromosome and Candidate gene as well as Locus. Within one scientific family, Teepu Siddique focuses on topics pertaining to Cell biology under SOD1, and may sometimes address concerns connected to Pathogenesis.

He most often published in these fields:

  • Amyotrophic lateral sclerosis (49.11%)
  • Genetics (43.75%)
  • SOD1 (20.09%)

What were the highlights of his more recent work (between 2012-2021)?

  • Amyotrophic lateral sclerosis (49.11%)
  • Genetics (43.75%)
  • Disease (12.95%)

In recent papers he was focusing on the following fields of study:

His main research concerns Amyotrophic lateral sclerosis, Genetics, Disease, Pathology and Cell biology. His Amyotrophic lateral sclerosis research is multidisciplinary, incorporating elements of C9orf72 and Neuroscience. Many of his research projects under Genetics are closely connected to Table with Table, tying the diverse disciplines of science together.

Teepu Siddique has included themes like Psychiatry and Bioinformatics in his Disease study. The various areas that Teepu Siddique examines in his Pathology study include Dermatology, Retinal, Central nervous system, Retina and Optic nerve. His studies in Cell biology integrate themes in fields like Transfection, Pathogenesis and LRRK2.

Between 2012 and 2021, his most popular works were:

  • Sporadic and hereditary amyotrophic lateral sclerosis (ALS). (120 citations)
  • Identification of TMEM230 mutations in familial Parkinson's disease (110 citations)
  • A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis (93 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Mutation
  • Internal medicine

Teepu Siddique mainly focuses on Amyotrophic lateral sclerosis, Neuroscience, C9orf72, Disease and Genetics. His research integrates issues of Neuromuscular disease and Age of onset in his study of Amyotrophic lateral sclerosis. His Neuroscience research includes elements of Mutation, Alzheimer's disease, Epigenetics and Proteasome.

His C9orf72 research is multidisciplinary, relying on both Neurodegeneration, Charged multivesicular body protein 2B, Proband and SOD1. The various areas that Teepu Siddique examines in his Disease study include Therapeutic strategy, Neurology, Intracellular and Bioinformatics. His work deals with themes such as Molecular biology and Pathogenesis, which intersect with Genetics.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

T. J. Kwiatkowski;D. A. Bosco;D. A. Bosco;A. L. LeClerc;A. L. LeClerc;E. Tamrazian.
Science (2009)

2662 Citations

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

Han Xiang Deng;Afif Hentati;John A. Tainer;Zafar Iqbal.
Science (1993)

1820 Citations

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia

Han-Xiang Deng;Wenjie Chen;Seong‐Tshool Hong;Seong‐Tshool Hong;Kym M Boycott.
Nature (2011)

1216 Citations

Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations

Ian R.A. Mackenzie;Eileen H. Bigio;Paul G. Ince;Felix Geser.
Annals of Neurology (2007)

1028 Citations

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis.

Yi Yang;Afif Hentati;Han Xiang Deng;Omar Dabbagh.
Nature Genetics (2001)

903 Citations

SQSTM1 mutations in familial and sporadic amyotrophic lateral sclerosis.

Faisal Fecto;Jianhua Yan;S. Pavan Vemula;Erdong Liu.
JAMA Neurology (2011)

655 Citations

Presence of dendritic cells, MCP-1, and activated microglia/macrophages in amyotrophic lateral sclerosis spinal cord tissue.

Jenny S. Henkel;Joseph I. Engelhardt;László Siklós;Ericka P. Simpson.
Annals of Neurology (2004)

569 Citations

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity.

T Siddique;D A Figlewicz;D A Figlewicz;M A Pericak-Vance;J L Haines.
The New England Journal of Medicine (1991)

516 Citations

Conversion to the amyotrophic lateral sclerosis phenotype is associated with intermolecular linked insoluble aggregates of SOD1 in mitochondria

Han Xiang Deng;Yong Shi;Yoshiaki Furukawa;Hong Zhai.
Proceedings of the National Academy of Sciences of the United States of America (2006)

506 Citations

Familial amyotrophic lateral sclerosis with frontotemporal dementia is linked to a locus on chromosome 9p13.2–21.3

Caroline Vance;Ammar Al-Chalabi;Deborah Ruddy;Bradley N. Smith.
Brain (2006)

457 Citations

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