Entries of Fujinami, Kaoru on the publication server
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Jump to: 2020
Number of items: 2.
2020
Runhart, Esmee H., Khan, Mubeen, Cornelis, Stéphanie S., Roosing, Susanne, Del Pozo-Valero, Marta, Lamey, Tina M., Liskova, Petra
, Roberts, Lisa
, Stöhr, Heidi, Klaver, Caroline C. W., Hoyng, Carel B., Cremers, Frans P. M., Dhaenens, Claire-Marie, AlTabishi, Alaa, Ayuso, Carmen, Banfi, Sandro, Ben-Yosef, Tamar, van den Born, L. Ingeborgh, Fakin, Ana, Farrar, G. Jane, Ferraz Sallum, Juliana Maria, Fujinami, Kaoru, Gorin, Michael B., Hlavata, Lucia, Kamakari, Smaragda, Kousal, Bohdan, MacDonald, Ian M., McLaren, Terri L., Matynia, Anna, Oldak, Monika, Podhajcer, Osvaldo L., Ramesar, Raj, De Roach, John N., Sharon, Dror, Simonelli, Francesca, Testa, Francesco, Thompson, Jennifer A., Tracewska, Anna M., Vincent, Andrea L. and Weber, Bernhard H. F.
(2020)
Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease.
JAMA Ophthalmology 138 (10), p. 1035.
Fulltext not available.
, Roberts, Lisa
, Stöhr, Heidi, Klaver, Caroline C. W., Hoyng, Carel B., Cremers, Frans P. M., Dhaenens, Claire-Marie, AlTabishi, Alaa, Ayuso, Carmen, Banfi, Sandro, Ben-Yosef, Tamar, van den Born, L. Ingeborgh, Fakin, Ana, Farrar, G. Jane, Ferraz Sallum, Juliana Maria, Fujinami, Kaoru, Gorin, Michael B., Hlavata, Lucia, Kamakari, Smaragda, Kousal, Bohdan, MacDonald, Ian M., McLaren, Terri L., Matynia, Anna, Oldak, Monika, Podhajcer, Osvaldo L., Ramesar, Raj, De Roach, John N., Sharon, Dror, Simonelli, Francesca, Testa, Francesco, Thompson, Jennifer A., Tracewska, Anna M., Vincent, Andrea L. and Weber, Bernhard H. F.
(2020)
Association of Sex With Frequent and Mild ABCA4 Alleles in Stargardt Disease.
JAMA Ophthalmology 138 (10), p. 1035.
Fulltext not available.
Khan, Mubeen, Cornelis, Stéphanie S., Pozo-Valero, Marta Del, Whelan, Laura, Runhart, Esmee H., Mishra, Ketan
, Bults, Femke, AlSwaiti, Yahya, AlTalbishi, Alaa, De Baere, Elfride, Banfi, Sandro, Banin, Eyal, Bauwens, Miriam, Ben-Yosef, Tamar, Boon, Camiel J. F., van den Born, L. Ingeborgh, Defoort, Sabine, Devos, Aurore, Dockery, Adrian
, Dudakova, Lubica
, Fakin, Ana, Farrar, G. Jane, Sallum, Juliana Maria Ferraz, Fujinami, Kaoru, Gilissen, Christian
, Glavač, Damjan, Gorin, Michael B., Greenberg, Jacquie, Hayashi, Takaaki, Hettinga, Ymkje M., Hoischen, Alexander
, Hoyng, Carel B., Hufendiek, Karsten, Jägle, Herbert, Kamakari, Smaragda, Karali, Marianthi, Kellner, Ulrich, Klaver, Caroline C. W., Kousal, Bohdan
, Lamey, Tina M., MacDonald, Ian M., Matynia, Anna, McLaren, Terri L., Mena, Marcela D.
, Meunier, Isabelle, Miller, Rianne, Newman, Hadas, Ntozini, Buhle, Oldak, Monika
, Pieterse, Marc, Podhajcer, Osvaldo L., Puech, Bernard, Ramesar, Raj, Rüther, Klaus, Salameh, Manar, Salles, Mariana Vallim, Sharon, Dror, Simonelli, Francesca, Spital, Georg, Steehouwer, Marloes, Szaflik, Jacek P., Thompson, Jennifer A., Thuillier, Caroline, Tracewska, Anna M.
, van Zweeden, Martine, Vincent, Andrea L., Zanlonghi, Xavier, Liskova, Petra
, Stöhr, Heidi, Roach, John N. De, Ayuso, Carmen, Roberts, Lisa
, Weber, Bernhard H. F., Dhaenens, Claire‐Marie and Cremers, Frans P. M.
(2020)
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.
Genetics in Medicine 22 (7), pp. 1235-1246.
Fulltext not available.
, Bults, Femke, AlSwaiti, Yahya, AlTalbishi, Alaa, De Baere, Elfride, Banfi, Sandro, Banin, Eyal, Bauwens, Miriam, Ben-Yosef, Tamar, Boon, Camiel J. F., van den Born, L. Ingeborgh, Defoort, Sabine, Devos, Aurore, Dockery, Adrian
, Dudakova, Lubica
, Fakin, Ana, Farrar, G. Jane, Sallum, Juliana Maria Ferraz, Fujinami, Kaoru, Gilissen, Christian
, Glavač, Damjan, Gorin, Michael B., Greenberg, Jacquie, Hayashi, Takaaki, Hettinga, Ymkje M., Hoischen, Alexander
, Hoyng, Carel B., Hufendiek, Karsten, Jägle, Herbert, Kamakari, Smaragda, Karali, Marianthi, Kellner, Ulrich, Klaver, Caroline C. W., Kousal, Bohdan
, Lamey, Tina M., MacDonald, Ian M., Matynia, Anna, McLaren, Terri L., Mena, Marcela D.
, Meunier, Isabelle, Miller, Rianne, Newman, Hadas, Ntozini, Buhle, Oldak, Monika
, Pieterse, Marc, Podhajcer, Osvaldo L., Puech, Bernard, Ramesar, Raj, Rüther, Klaus, Salameh, Manar, Salles, Mariana Vallim, Sharon, Dror, Simonelli, Francesca, Spital, Georg, Steehouwer, Marloes, Szaflik, Jacek P., Thompson, Jennifer A., Thuillier, Caroline, Tracewska, Anna M.
, van Zweeden, Martine, Vincent, Andrea L., Zanlonghi, Xavier, Liskova, Petra
, Stöhr, Heidi, Roach, John N. De, Ayuso, Carmen, Roberts, Lisa
, Weber, Bernhard H. F., Dhaenens, Claire‐Marie and Cremers, Frans P. M.
(2020)
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics.
Genetics in Medicine 22 (7), pp. 1235-1246.
Fulltext not available.
