His scientific interests lie mostly in Genetics, Mutation, Internal medicine, Exome sequencing and Endocrinology. Candidate gene, Gene, Missense mutation, Frameshift mutation and Exon are among the areas of Genetics where Tim M. Strom concentrates his study. His Mutation research is multidisciplinary, relying on both Bioinformatics, Phenotype, Polydactyly, Ellis–van Creveld syndrome and Pedigree chart.
His Coronary artery disease, Myocardial infarction and Congenital adrenal hypoplasia study in the realm of Internal medicine connects with subjects such as Generalized arterial calcification. His work on Exome as part of his general Exome sequencing study is frequently connected to VPS35, thereby bridging the divide between different branches of science. The KCNJ5 research Tim M. Strom does as part of his general Endocrinology study is frequently linked to other disciplines of science, such as Hypophosphatemic Rickets, Autosomal dominant hypophosphatemic rickets and Familial hyperaldosteronism, therefore creating a link between diverse domains of science.
The scientist’s investigation covers issues in Genetics, Exome sequencing, Mutation, Internal medicine and Missense mutation. His study in Gene, Phenotype, Intellectual disability, Exon and Frameshift mutation is carried out as part of his Genetics studies. As a member of one scientific family, Tim M. Strom mostly works in the field of Exome sequencing, focusing on Compound heterozygosity and, on occasion, Pathology and Mitochondrial disease.
His research investigates the connection with Mutation and areas like Molecular biology which intersect with concerns in Mutant. His Internal medicine research includes elements of Endocrinology and Oncology. Tim M. Strom interconnects Disease gene identification and Allele in the investigation of issues within Missense mutation.
Tim M. Strom focuses on Genetics, Exome sequencing, Missense mutation, Gene and Phenotype. His research in Intellectual disability, Haploinsufficiency, Mitochondrial disease, Exon and Microcephaly are components of Genetics. The various areas that he examines in his Exon study include Sanger sequencing, Proband and Mutation.
His Exome sequencing research incorporates elements of Bioinformatics, Medical genetics, Disease, Dystonia and Candidate gene. Tim M. Strom studied Missense mutation and Spasticity that intersect with Hereditary spastic paraplegia, Mitochondrion and Allele. His research integrates issues of Molecular biology, Amyotrophic lateral sclerosis and Computational biology in his study of Gene.
Genetics, Exome sequencing, Gene, Phenotype and Missense mutation are his primary areas of study. His Genetics research focuses on Intellectual disability, Frameshift mutation, Protein subunit, DNA sequencing and Nuclear DNA. Tim M. Strom mostly deals with Exome in his studies of Exome sequencing.
The study incorporates disciplines such as Amyotrophic lateral sclerosis, Browning and Brown Adipocytes in addition to Gene. His study in Phenotype is interdisciplinary in nature, drawing from both Hypotonia, Cardiomyopathy and Disease. His Missense mutation research integrates issues from Spastic and Immune system.
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Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology
Alexander Zimprich;Alexander Zimprich;Saskia Biskup;Petra Leitner;Peter Lichtner.
Genomewide association analysis of coronary artery disease.
Nilesh J. Samani;Jeanette Erdmann;Alistair S. Hall;Christian Hengstenberg.
The New England Journal of Medicine (2007)
Autosomal dominant hypophosphataemic rickets is associated with mutations in FGF23
Kenneth E. White;Wayne E. Evans;Jeffery L.H. O'Riordan;Marcy C. Speer.
Nature Genetics (2000)
Transcriptome and genome sequencing uncovers functional variation in humans
Tuuli Lappalainen;Michael Sammeth;Marc R. Friedländer;Peter A. C. ‘t Hoen.
Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2
Simone Rost;Andreas Fregin;Vytautas Ivaskevicius;Ernst Conzelmann.
The genetic architecture of type 2 diabetes
Christian Fuchsberger;Christian Fuchsberger;Jason A. Flannick;Jason A. Flannick;Tanya M. Teslovich;Anubha Mahajan.
Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment
Elisabeth B Binder;Daria Salyakina;Peter Lichtner;Gabriele M Wochnik.
Nature Genetics (2004)
Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine.
Martin Dichgans;Tobias Freilinger;Gertrud Eckstein;Elena Babini.
The Lancet (2005)
An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita
Elena Zanaria;Françoise Muscatelli;Barbara Bardoni;Tim M. Strom.
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study.
Anita Rauch;Dagmar Wieczorek;Elisabeth Graf;Thomas Wieland.
The Lancet (2012)
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