B. Gelb

Genetics · 2001–2017

A researcher in the Science corpus: 10 papers; trusts 1 researcher and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 45 citations into it
• Immunology — 10 citations into it
• Cellular and Molecular Neuroscience — 7 citations into it

Whom B. Gelb trusts

Their strongest outbound trust, strongest first, inferred from their citations.

1. T. Préat (in Cellular and Molecular Neuroscience)

Papers from B. Gelb's perspective

Ordered by how strongly the researchers B. Gelb trusts endorse each paper. Same corpus, a different order for every researcher.

1. The nonreceptor protein tyrosine phosphatase corkscrew functions in multiple receptor tyrosine kinase pathways in Drosophila.
2. Denaturing high‐performance liquid chromatography: A review (Human Mutation)
3. CHARMM: A program for macromolecular energy, minimization, and dynamics calculations
4. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia (Nature Genetics)
5. The MEK1–ERK1/2 signaling pathway promotes compensated cardiac hypertrophy in transgenic mice (EMBO Journal)
6. Localization of Long-Term Memory Within the Drosophila Mushroom Body
7. The RAF proteins take centre stage (Nature reviews. Molecular cell biology)
8. Mechanism of activation of the RAF-ERK signaling pathway by oncogenic mutations of B-RAF.
9. ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
10. Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema (Nature Genetics)

Their papers

• Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy (2007) — 671 citations
• Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome (2001) — 1,671 citations
• De novo mutations in histone modifying genes in congenital heart disease (2013) — 900 citations
• Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia (2003) — 1,030 citations
• Spacing Effect: SHP2 Phosphatase Regulates Resting Intervals Between Learning Trials in Long-Term Memory Induction (2009) — 153 citations
• Contribution of rare inherited and de novo variants in 2,871 congenital heart disease probands (2017) — 773 citations
• Genetic basis for congenital heart defects: current knowledge: a scientific statement from the American Heart Association Congenital Cardiac Defects Committee, Council on Cardiovascular Disease in the Young: endorsed by the American Academy of Pediatrics. (2007) — 836 citations
• De novo mutations in Congenital Heart Disease with Neurodevelopmental and Other Birth Defects (2015) — 730 citations
• Noonan Syndrome: Clinical Features, Diagnosis, and Management Guidelines (2010) — 611 citations
• PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity. (2002) — 772 citations