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| Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 nvel loci and several mutation hotspots |
| Authors: Kuss, Andreas Walter; Garshasbi, Masoud; Kahrizi, Kimia; Tzschach, Andreas; Behjati, Farkhondeh; Darvish, Hossein; Abbasi-Moheb, Lia; Puettmann, Lucia; Zecha, Agnes; Weißmann, Robert; Hu, Hao; Mohseni, Marzieh; Abedini, Seyedeh Sedigheh; Rajab, Anna; Hertzberg, Christoph; Wieczorek, Dagmar; Ullmann, Reinhard; Saghar Ghasemi-Firouzabadi, Saghar; Banihashemi, Susan; Arzhangi, Sanaz; Hadavi, Valeh; Bahrami-Monajemi, Gholamreza; Kasiri, Mahboubeh; Falah, Masoumeh; Nikuei, Pooneh; Dehghan, Atefeh; Sobhani, Masoumeh; Jamali, Payman; Ropers, Hans-Hilger; Najmabadi, Hossein | | Date of Publication (YYYY-MM-DD): 2010-11-09 | | Title of Journal: Human Genetics | | Volume: 129 | | Issue / Number: 2 | | Start Page: 141 | | End Page: 148 | | Document Type: Article | | ID: 533429.0 |
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| Fragile X syndrome screening of families with consanguineous and non-consanguineous parents in the Iranian population |
| Authors: Pouya, Ali Reza; Abedini, Seyedeh Sedigheh; Mansoorian, Neda; Behjati, Farkhondeh; Nikzat, Nooshin; Mohseni, Marzieh; Nieh, Sahar Esmaeeli; Moheb, Lia Abbasi; Darvish, Hossein; Monajemi, Gholamreza Bahrami; Banihashemi, Susan; Kahrizi, Kimia; Ropers, Hans-Hilger; Najmabadi, Hossein | | Date of Publication (YYYY-MM-DD): 2009-04 | | Title of Journal: European Journal of Medical Genetics | | Volume: 52 | | Issue / Number: 4 | | Start Page: 170 | | End Page: 173 | | Document Type: Article | | ID: 473414.0 |
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| A defect in the TUSC3 gene is associated with autosomal recessive mental retardation |
| Authors: Garshasbi, Masoud; Hadavi, Valeh; Habibi, Haleh; Kahrizi, Kimia; Kariminejad, Roxana; Behjati, Farkhondeh; Tzschach, Andreas; Najmabadi, Hossein; Ropers, Hans-Hilger; Kuss, Andreas Walter | | Date of Publication (YYYY-MM-DD): 2008-05-01 | | Title of Journal: The American Journal of Human Genetics | | Volume: 82 | | Issue / Number: 5 | | Start Page: 1158 | | End Page: 1164 | | Document Type: Article | | ID: 408332.0 |
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| Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. |
| Authors: Najmabadi, Hossein; Motazacker, Mohammad Mahdi; Garshasbi, Masoud; Kahrizi, Kimia; Tzschach, Andreas; Chen, Wei; Behjati, Farkhondeh; Hadavi, Valeh; Nieh, Sahar Esmaeeli; Abedini, Seyedeh Sedigheh; Vazifehmand, Reza; Firouzabadi, Saghar Ghasemi; Jamali, Payman; Falah, Masoumeh; Seifati, Seyed Morteza; Grüters, Annette; Lenzner, Steffen; Jensen, Lars R.; Rüschendorf, Franz; Kuss, Andreas W.; Ropers, Hans-Hilger | | Date of Publication (YYYY-MM-DD): 2007-03-01 | | Title of Journal: Human Genetics | | Volume: 121 | | Issue / Number: 1 | | Start Page: 43 | | End Page: 48 | | Document Type: Article | | ID: 334609.0 |
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| SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly |
| Authors: Garshasbi, Masoud; Motazacker, Mohammad Mahdi; Kahrizi, Kimia; Behjati, Farkhondeh; Abedini, Seyedeh Sedigheh; Nieh, Sahar Esmaeeli; Firouzabadi, Saghar Ghasemi; Becker, Christian; Rüschendorf, Franz; Nürnberg, Peter; Tzschach, Andreas; Vazifehmand, Reza; Erdogan, Fikret; Ullmann, Reinhard; Lenzner, Steffen; Kuss, Andreas W.; Ropers, Hans-Hilger; Najmabadi, Hossein | | Date of Publication (YYYY-MM-DD): 2006-02-01 | | Title of Journal: Human Genetics | | Volume: 118 | | Issue / Number: 6 | | Start Page: 708 | | End Page: 715 | | Document Type: Article | | ID: 307622.0 |
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