His primary scientific interests are in Genetics, Gene, Mutation, Molecular biology and Allele. Genetics is frequently linked to Autism in his study. Steve S. Sommer combines subjects such as Receptor and DNA with his study of Gene.
In his research on the topic of Mutation, Cancer research is strongly related with Breast cancer. His Molecular biology research is multidisciplinary, incorporating elements of Biochemistry and Polymerase chain reaction, Primer. His work carried out in the field of Allele brings together such families of science as Odds ratio, Schizophrenia and Bioinformatics.
The scientist’s investigation covers issues in Genetics, Gene, Molecular biology, Mutation and Allele. His study in Germline mutation, Factor IX, Exon, Missense mutation and Mutation falls within the category of Genetics. His research in Germline mutation intersects with topics in Mutation rate and Germline.
Many of his studies involve connections with topics such as Cancer research and Gene. Steve S. Sommer has included themes like Mutant, Oligonucleotide, DNA, DNA polymerase and Polymerase chain reaction in his Molecular biology study. His Mutation research incorporates elements of genomic DNA, Breast cancer, Mutagen and Carcinogenesis.
His primary areas of study are Genetics, Gene, Mutation, Molecular biology and Allele. As part of his studies on Genetics, he often connects relevant subjects like Autism. His study looks at the relationship between Gene and fields such as DNA, as well as how they intersect with chemical problems.
His Mutation study combines topics in areas such as Cancer, Breast cancer and INDEL Mutation. His biological study spans a wide range of topics, including Carcinogenesis, REV1, Oligonucleotide and DNA polymerase. His research investigates the connection between Allele and topics such as Bioinformatics that intersect with issues in microRNA, Schizophrenia, Attributable risk, Diagnosis of schizophrenia and Psychosis.
His primary areas of investigation include Genetics, Autism, Gene, Mutation and Bioinformatics. He integrates several fields in his works, including Genetics and Context. Many of his research projects under Autism are closely connected to Neuroligin with Neuroligin, tying the diverse disciplines of science together.
Steve S. Sommer conducts interdisciplinary study in the fields of Gene and Neurexin through his works. His Mutation study combines topics from a wide range of disciplines, such as Family history and Germline. His Bioinformatics study integrates concerns from other disciplines, such as Schizophrenia, microRNA and Point mutation.
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.
The "megaprimer" method of site-directed mutagenesis.
G Sarkar;S S Sommer.
BioTechniques (1990)
Beyond Li Fraumeni Syndrome: Clinical Characteristics of Families With p53 Germline Mutations
Kelly D. Gonzalez;Katie A. Noltner;Carolyn H. Buzin;Dongqing Gu.
Journal of Clinical Oncology (2009)
Blind analysis of denaturing high-performance liquid chromatography as a tool for mutation detection
Michael C. O'Donovan;Peter J. Oefner;Stacy C. Roberts;Jehannine Austin.
Genomics (1998)
SNPs in human miRNA genes affect biogenesis and function.
Guihua Sun;Jin Yan;Katie Noltner;Jinong Feng.
RNA (2009)
Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity.
Gobinda Sarkar;Steve S. Sommer.
Science (1989)
Formamide can dramatically improve the specificity of PCR.
Gobinda Sarkar;Stephen Kapelner;Steve S. Sommer.
Nucleic Acids Research (1990)
Haemophilia B: database of point mutations and short additions and deletions, 7th edition.
F. Giannelli;P. M. Green;S. S. Sommer;M.-C. Poon.
Nucleic Acids Research (1990)
High frequency of neurexin 1beta signal peptide structural variants in patients with autism
Steve S. Sommer;Jinong Feng;Jin Yan.
Neuroscience Letters (2007)
Familial deletion within NLGN4 associated with autism and Tourette syndrome
Amy Lawson-Yuen;Juan-Sebastian Saldivar;Steve Sommer;Jonathan Picker.
European Journal of Human Genetics (2008)
Analysis of the neuroligin 3 and 4 genes in autism and other neuropsychiatric patients.
J. Yan;G. Oliveira;A. Coutinho;C. Yang.
Molecular Psychiatry (2005)
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