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The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia.
Published in:
Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31436-8
By:
- Nehme, Ralda;
- Pietiläinen, Olli;
- Artomov, Mykyta;
- Tegtmeyer, Matthew;
- Valakh, Vera;
- Lehtonen, Leevi;
- Bell, Christina;
- Singh, Tarjinder;
- Trehan, Aditi;
- Sherwood, John;
- Manning, Danielle;
- Peirent, Emily;
- Malik, Rhea;
- Guss, Ellen J.;
- Hawes, Derek;
- Beccard, Amanda;
- Bara, Anne M.;
- Hazelbaker, Dane Z.;
- Zuccaro, Emanuela;
- Genovese, Giulio
Publication type:
Article
Deep learning based phenotyping of medical images improves power for gene discovery of complex disease.
Published in:
NPJ Digital Medicine, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s41746-023-00903-x
By:
- Flynn, Brianna I.;
- Javan, Emily M.;
- Lin, Eugenia;
- Trutner, Zoe;
- Koenig, Karl;
- Anighoro, Kenoma O.;
- Kun, Eucharist;
- Gupta, Alaukik;
- Singh, Tarjinder;
- Jayakumar, Prakash;
- Narasimhan, Vagheesh M.
Publication type:
Article
Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania.
Published in:
PLoS ONE, 2014, v. 9, n. 11, p. 1, doi. 10.1371/journal.pone.0111464
By:
- Mtatiro, Siana Nkya;
- Singh, Tarjinder;
- Rooks, Helen;
- Mgaya, Josephine;
- Mariki, Harvest;
- Soka, Deogratius;
- Mmbando, Bruno;
- Msaki, Evarist;
- Kolder, Iris;
- Thein, Swee Lay;
- Menzel, Stephan;
- Cox, Sharon E.;
- Makani, Julie;
- Barrett, Jeffrey C.
Publication type:
Article
Contribution of retrotransposition to developmental disorders.
Published in:
Nature Communications, 2019, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41467-019-12520-y
By:
- Gardner, Eugene J.;
- Prigmore, Elena;
- Gallone, Giuseppe;
- Danecek, Petr;
- Samocha, Kaitlin E.;
- Handsaker, Juliet;
- Gerety, Sebastian S.;
- Ironfield, Holly;
- Short, Patrick J.;
- Sifrim, Alejandro;
- Singh, Tarjinder;
- Chandler, Kate E.;
- Clement, Emma;
- Lachlan, Katherine L.;
- Prescott, Katrina;
- Rosser, Elisabeth;
- FitzPatrick, David R.;
- Firth, Helen V.;
- Hurles, Matthew E.
Publication type:
Article
Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing.
Published in:
2017
By:
- Artomov, Mykyta;
- Stratigos, Alexander J;
- Kim, Ivana;
- Kumar, Raj;
- Lauss, Martin;
- Reddy, Bobby Y;
- Miao, Benchun;
- Daniela Robles-Espinoza, Carla;
- Sankar, Aravind;
- Njauw, Ching-Ni;
- Shannon, Kristen;
- Gragoudas, Evangelos S;
- Marie Lane, Anne;
- Iyer, Vivek;
- Newton-Bishop, Julia A;
- Timothy Bishop, D;
- Holland, Elizabeth A;
- Mann, Graham J;
- Singh, Tarjinder;
- Daly, Mark J
Publication type:
journal article
Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer.
Published in:
BMC Medical Genetics, 2015, v. 16, n. 1, p. 1, doi. 10.1186/s12881-015-0148-3
By:
- Mtatiro, Siana N.;
- Mgaya, Josephine;
- Singh, Tarjinder;
- Mariki, Harvest;
- Rooks, Helen;
- Soka, Deogratius;
- Mmbando, Bruno;
- Thein, Swee Lay;
- Barrett, Jeffrey C.;
- Makani, Julie;
- Cox, Sharon E.;
- Menzel, Stephan
Publication type:
Article

Found: 6

The 22q11.2 region regulates presynaptic gene-products linked to schizophrenia.

Deep learning based phenotyping of medical images improves power for gene discovery of complex disease.

Genome Wide Association Study of Fetal Hemoglobin in Sickle Cell Anemia in Tanzania.

Contribution of retrotransposition to developmental disorders.

Rare Variant, Gene-Based Association Study of Hereditary Melanoma Using Whole-Exome Sequencing.

Genetic association of fetal-hemoglobin levels in individuals with sickle cell disease in Tanzania maps to conserved regulatory elements within the MYB core enhancer.