His study deals with a combination of Genetics and Evolutionary biology. Menachem Fromer integrates Evolutionary biology and Genetics in his research. His research on Gene frequently connects to adjacent areas such as Nonsense. Menachem Fromer regularly links together related areas like Schizophrenia (object-oriented programming) in his Psychiatry studies. His Schizophrenia (object-oriented programming) study frequently draws connections between related disciplines such as Psychiatry. He integrates many fields, such as Exome sequencing and Genome-wide association study, in his works. His work blends Genome-wide association study and Structural variation studies together. Menachem Fromer connects Structural variation with Exome sequencing in his study. Exome and Phenotype are frequently intertwined in his study.
In his work, Menachem Fromer performs multidisciplinary research in Genetics and Neuroscience. He merges Neuroscience with Genetics in his study. In his research, he undertakes multidisciplinary study on Gene and Gene expression. Menachem Fromer regularly ties together related areas like Phenotype in his Exome sequencing studies. He undertakes multidisciplinary investigations into Phenotype and Genotype in his work. Menachem Fromer brings together Genotype and Genome to produce work in his papers. While working on this project, Menachem Fromer studies both Genome and Copy-number variation. He conducts interdisciplinary study in the fields of Copy-number variation and Exome sequencing through his research. Menachem Fromer conducts interdisciplinary study in the fields of Computational biology and Gene through his research.
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Analysis of protein-coding genetic variation in 60,706 humans
Monkol Lek;Konrad J. Karczewski;Konrad J. Karczewski;Eric V. Minikel;Eric V. Minikel;Kaitlin E. Samocha.
Biological insights from 108 schizophrenia-associated genetic loci
Stephan Ripke;Stephan Ripke;Benjamin M. Neale;Benjamin M. Neale;Aiden Corvin;James T. R. Walters.
Clonal Hematopoiesis and Blood-Cancer Risk Inferred from Blood DNA Sequence
Giulio Genovese;Anna K. Kähler;Robert E. Handsaker;Johan Lindberg.
The New England Journal of Medicine (2014)
Synaptic, transcriptional and chromatin genes disrupted in autism
Silvia De Rubeis;Xin-Xin He;Arthur P Goldberg;Christopher S. Poultney.
Patterns and rates of exonic de novo mutations in autism spectrum disorders
Benjamin M. Neale;Yan Kou;Li Liu;Avi Ma'Ayan.
Genome-wide association analysis identifies 13 new risk loci for schizophrenia
Stephan Ripke;Stephan Ripke;Colm T. O'Dushlaine;Kimberly D. Chambert;Jennifer L. Moran.
Nature Genetics (2013)
De novo mutations in schizophrenia implicate synaptic networks
Menachem Fromer;Andrew Pocklington;David Kavanagh;Hywel John Williams.
A polygenic burden of rare disruptive mutations in schizophrenia
Shaun M Purcell;Jennifer L Moran;Menachem Fromer;Douglas Ruderfer.
A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes
Daniel G. MacArthur;Daniel G. MacArthur;Suganthi Balasubramanian;Adam Frankish;Ni Huang.
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Bjarni J. Vilhjálmsson;Jian Yang;Hilary K. Finucane;Alexander Gusev.
American Journal of Human Genetics (2015)
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