المؤلفون: Evin M. Padhi (11129998), Tristan J. Hayeck (11130001), Zhang Cheng (802884), Sumantra Chatterjee (11130004), Brandon J. Mannion (11130007), Marta Byrska-Bishop (11130010), Marjolaine Willems (8882330), Lucile Pinson (11130013), Sylvia Redon (11130016), Caroline Benech (204323), Kevin Uguen (11130019), Séverine Audebert-Bellanger (10930066), Cédric Le Marechal (11130022), Claude Férec (204332), Stephanie Efthymiou (4569349), Fatima Rahman (11130025), Shazia Maqbool (11130028), Reza Maroofian (5237852), Henry Houlden (110428), Rajeeva Musunuri (11130031), Giuseppe Narzisi (107365), Avinash Abhyankar (140166), Riana D. Hunter (5320184), Jennifer Akiyama (11130034), Lauren E. Fries (11130037), Jeffrey K. Ng (11130040), Elvisa Mehinovic (11130043), Nick Stong (11130046), Andrew S. Allen (11130049), Diane E. Dickel (4379629), Raphael A. Bernier (5016758), David U. Gorkin (8571390), Len A. Pennacchio (10721833), Michael C. Zody (11130052), Tychele N. Turner (11130055)

مصطلحات موضوعية: Genetics, Autism, Neurodevelopmental disorder, Enhancer, Gene regulatory network, EBF3, hs737, Genome, Variant, De novo

Relation: https://figshare.com/articles/journal_contribution/Additional_file_2_of_Coding_and_noncoding_variants_in_EBF3_are_involved_in_HADDS_and_simplex_autism/14978464

الاتاحة: https://doi.org/10.6084/m9.figshare.14978464.v1

المؤلفون: Evin M. Padhi (11129998), Tristan J. Hayeck (11130001), Zhang Cheng (802884), Sumantra Chatterjee (11130004), Brandon J. Mannion (11130007), Marta Byrska-Bishop (11130010), Marjolaine Willems (8882330), Lucile Pinson (11130013), Sylvia Redon (11130016), Caroline Benech (204323), Kevin Uguen (11130019), Séverine Audebert-Bellanger (10930066), Cédric Le Marechal (11130022), Claude Férec (204332), Stephanie Efthymiou (4569349), Fatima Rahman (11130025), Shazia Maqbool (11130028), Reza Maroofian (5237852), Henry Houlden (110428), Rajeeva Musunuri (11130031), Giuseppe Narzisi (107365), Avinash Abhyankar (140166), Riana D. Hunter (5320184), Jennifer Akiyama (11130034), Lauren E. Fries (11130037), Jeffrey K. Ng (11130040), Elvisa Mehinovic (11130043), Nick Stong (11130046), Andrew S. Allen (11130049), Diane E. Dickel (4379629), Raphael A. Bernier (5016758), David U. Gorkin (8571390), Len A. Pennacchio (10721833), Michael C. Zody (11130052), Tychele N. Turner (11130055)

مصطلحات موضوعية: Genetics, Autism, Neurodevelopmental disorder, Enhancer, Gene regulatory network, EBF3, hs737, Genome, Variant, De novo

Relation: https://figshare.com/articles/dataset/Additional_file_1_of_Coding_and_noncoding_variants_in_EBF3_are_involved_in_HADDS_and_simplex_autism/14978458

الاتاحة: https://doi.org/10.6084/m9.figshare.14978458.v1

المؤلفون: Evin M. Padhi (11129998), Tristan J. Hayeck (11130001), Zhang Cheng (802884), Sumantra Chatterjee (11130004), Brandon J. Mannion (11130007), Marta Byrska-Bishop (11130010), Marjolaine Willems (8882330), Lucile Pinson (11130013), Sylvia Redon (11130016), Caroline Benech (204323), Kevin Uguen (11130019), Séverine Audebert-Bellanger (10930066), Cédric Le Marechal (11130022), Claude Férec (204332), Stephanie Efthymiou (4569349), Fatima Rahman (11130025), Shazia Maqbool (11130028), Reza Maroofian (5237852), Henry Houlden (110428), Rajeeva Musunuri (11130031), Giuseppe Narzisi (107365), Avinash Abhyankar (140166), Riana D. Hunter (5320184), Jennifer Akiyama (11130034), Lauren E. Fries (11130037), Jeffrey K. Ng (11130040), Elvisa Mehinovic (11130043), Nick Stong (11130046), Andrew S. Allen (11130049), Diane E. Dickel (4379629), Raphael A. Bernier (5016758), David U. Gorkin (8571390), Len A. Pennacchio (10721833), Michael C. Zody (11130052), Tychele N. Turner (11130055)

مصطلحات موضوعية: Genetics, Autism, Neurodevelopmental disorder, Enhancer, Gene regulatory network, EBF3, hs737, Genome, Variant, De novo

Relation: https://figshare.com/articles/dataset/Additional_file_3_of_Coding_and_noncoding_variants_in_EBF3_are_involved_in_HADDS_and_simplex_autism/14978467

الاتاحة: https://doi.org/10.6084/m9.figshare.14978467.v1

المؤلفون: Evin M. Padhi (11129998), Tristan J. Hayeck (11130001), Zhang Cheng (802884), Sumantra Chatterjee (11130004), Brandon J. Mannion (11130007), Marta Byrska-Bishop (11130010), Marjolaine Willems (8882330), Lucile Pinson (11130013), Sylvia Redon (11130016), Caroline Benech (204323), Kevin Uguen (11130019), Séverine Audebert-Bellanger (10930066), Cédric Le Marechal (11130022), Claude Férec (204332), Stephanie Efthymiou (4569349), Fatima Rahman (11130025), Shazia Maqbool (11130028), Reza Maroofian (5237852), Henry Houlden (110428), Rajeeva Musunuri (11130031), Giuseppe Narzisi (107365), Avinash Abhyankar (140166), Riana D. Hunter (5320184), Jennifer Akiyama (11130034), Lauren E. Fries (11130037), Jeffrey K. Ng (11130040), Elvisa Mehinovic (11130043), Nick Stong (11130046), Andrew S. Allen (11130049), Diane E. Dickel (4379629), Raphael A. Bernier (5016758), David U. Gorkin (8571390), Len A. Pennacchio (10721833), Michael C. Zody (11130052), Tychele N. Turner (11130055)

مصطلحات موضوعية: Genetics, Autism, Neurodevelopmental disorder, Enhancer, Gene regulatory network, EBF3, hs737, Genome, Variant, De novo

Relation: https://figshare.com/articles/dataset/Additional_file_5_of_Coding_and_noncoding_variants_in_EBF3_are_involved_in_HADDS_and_simplex_autism/14978476

الاتاحة: https://doi.org/10.6084/m9.figshare.14978476.v1

المؤلفون: Evin M. Padhi (11129998), Tristan J. Hayeck (11130001), Zhang Cheng (802884), Sumantra Chatterjee (11130004), Brandon J. Mannion (11130007), Marta Byrska-Bishop (11130010), Marjolaine Willems (8882330), Lucile Pinson (11130013), Sylvia Redon (11130016), Caroline Benech (204323), Kevin Uguen (11130019), Séverine Audebert-Bellanger (10930066), Cédric Le Marechal (11130022), Claude Férec (204332), Stephanie Efthymiou (4569349), Fatima Rahman (11130025), Shazia Maqbool (11130028), Reza Maroofian (5237852), Henry Houlden (110428), Rajeeva Musunuri (11130031), Giuseppe Narzisi (107365), Avinash Abhyankar (140166), Riana D. Hunter (5320184), Jennifer Akiyama (11130034), Lauren E. Fries (11130037), Jeffrey K. Ng (11130040), Elvisa Mehinovic (11130043), Nick Stong (11130046), Andrew S. Allen (11130049), Diane E. Dickel (4379629), Raphael A. Bernier (5016758), David U. Gorkin (8571390), Len A. Pennacchio (10721833), Michael C. Zody (11130052), Tychele N. Turner (11130055)

مصطلحات موضوعية: Genetics, Autism, Neurodevelopmental disorder, Enhancer, Gene regulatory network, EBF3, hs737, Genome, Variant, De novo

Relation: https://figshare.com/articles/dataset/Additional_file_4_of_Coding_and_noncoding_variants_in_EBF3_are_involved_in_HADDS_and_simplex_autism/14978473

الاتاحة: https://doi.org/10.6084/m9.figshare.14978473.v1

المؤلفون: Evin M. Padhi (11129998), Tristan J. Hayeck (11130001), Zhang Cheng (802884), Sumantra Chatterjee (11130004), Brandon J. Mannion (11130007), Marta Byrska-Bishop (11130010), Marjolaine Willems (8882330), Lucile Pinson (11130013), Sylvia Redon (11130016), Caroline Benech (204323), Kevin Uguen (11130019), Séverine Audebert-Bellanger (10930066), Cédric Le Marechal (11130022), Claude Férec (204332), Stephanie Efthymiou (4569349), Fatima Rahman (11130025), Shazia Maqbool (11130028), Reza Maroofian (5237852), Henry Houlden (110428), Rajeeva Musunuri (11130031), Giuseppe Narzisi (107365), Avinash Abhyankar (140166), Riana D. Hunter (5320184), Jennifer Akiyama (11130034), Lauren E. Fries (11130037), Jeffrey K. Ng (11130040), Elvisa Mehinovic (11130043), Nick Stong (11130046), Andrew S. Allen (11130049), Diane E. Dickel (4379629), Raphael A. Bernier (5016758), David U. Gorkin (8571390), Len A. Pennacchio (10721833), Michael C. Zody (11130052), Tychele N. Turner (11130055)

مصطلحات موضوعية: Genetics, Autism, Neurodevelopmental disorder, Enhancer, Gene regulatory network, EBF3, hs737, Genome, Variant, De novo

Relation: https://figshare.com/articles/dataset/Additional_file_6_of_Coding_and_noncoding_variants_in_EBF3_are_involved_in_HADDS_and_simplex_autism/14978479

الاتاحة: https://doi.org/10.6084/m9.figshare.14978479.v1