受强制性开放获取政策约束的文章 - Suleyman Gulsuner, MD, PhD了解详情
无法在其他位置公开访问的文章：2 篇
Diagnostic yield of chromosomal microarray and trio whole exome sequencing in cryptogenic cerebral palsy
M Yechieli, S Gulsuner, H Ben-Pazi, A Fattal, A Aran, A Kuzminsky, L Sagi, ...
Journal of Medical Genetics 59 (8), 759-767, 2022
强制性开放获取政策： US National Institutes of Health
A defect in GPI synthesis as a suggested mechanism for the role of ARV1 in intellectual disability and seizures
R Segel, A Aran, S Gulsuner, H Nakamura, T Rosen, T Walsh, H Denda, ...
neurogenetics 21, 259-267, 2020
强制性开放获取政策： US National Institutes of Health
可在其他位置公开访问的文章：46 篇
Inherited mutations in women with ovarian carcinoma
BM Norquist, MI Harrell, MF Brady, T Walsh, MK Lee, S Gulsuner, ...
JAMA oncology 2 (4), 482-490, 2016
强制性开放获取政策： US National Institutes of Health
Spatial and temporal mapping of de novo mutations in schizophrenia to a fetal prefrontal cortical network
S Gulsuner, T Walsh, AC Watts, MK Lee, AM Thornton, S Casadei, ...
Cell 154 (3), 518-529, 2013
强制性开放获取政策： US National Institutes of Health
Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy
MY Zhang, JE Churpek, SB Keel, T Walsh, MK Lee, KR Loeb, S Gulsuner, ...
Nature Genetics, doi:10.1038/ng.3177, 2015
强制性开放获取政策： US National Institutes of Health
Mutations in homologous recombination genes and outcomes in ovarian carcinoma patients in GOG 218: an NRG oncology/gynecologic oncology group study
BM Norquist, MF Brady, MI Harrell, T Walsh, MK Lee, S Gulsuner, ...
Clinical Cancer Research 24 (4), 777-783, 2018
强制性开放获取政策： US Department of Defense, US National Institutes of Health, V Foundation, USA
Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variants
JJ Johnston, JJ van der Smagt, JA Rosenfeld, AT Pagnamenta, A Alswaid, ...
Genetics in Medicine 20 (10), 1175-1185, 2018
强制性开放获取政策： US National Institutes of Health, National Institute for Health Research, UK …
Genetic features of myelodysplastic syndrome and aplastic anemia in pediatric and young adult patients
SB Keel, A Scott, M Sanchez-Bonilla, PA Ho, S Gulsuner, CC Pritchard, ...
Haematologica 101 (11), 1343, 2016
强制性开放获取政策： US National Institutes of Health
Inherited predisposition to malignant mesothelioma and overall survival following platinum chemotherapy
R Hassan, B Morrow, A Thomas, T Walsh, MK Lee, S Gulsuner, ...
Proceedings of the National Academy of Sciences 116 (18), 9008-9013, 2019
强制性开放获取政策： US National Institutes of Health
Genomic analysis of bone marrow failure and myelodysplastic syndromes reveals phenotypic and diagnostic complexity.
MY Zhang, SB Keel, T Walsh, MK Lee, S Gulsuner, AC Watts, ...
Haematologica 100 (1), 42-48, 2015
强制性开放获取政策： US National Institutes of Health
Missense mutation in the ATPase, aminophospholipid transporter protein ATP8A2 is associated with cerebellar atrophy and quadrupedal locomotion
O Emre Onat, S Gulsuner, K Bilguvar, A Nazli Basak, H Topaloglu, M Tan, ...
European Journal of Human Genetics 21 (3), 281-285, 2013
强制性开放获取政策： US National Institutes of Health
Genetics of schizophrenia in the South African Xhosa
S Gulsuner, DJ Stein, ES Susser, G Sibeko, A Pretorius, T Walsh, ...
Science 367 (6477), 569-573, 2020
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Inherited breast cancer in Nigerian women
Y Zheng, T Walsh, S Gulsuner, S Casadei, MK Lee, TO Ogundiran, ...
Journal of clinical oncology 36 (28), 2820-2825, 2018
强制性开放获取政策： US National Institutes of Health, Susan G. Komen
Essential Role of BRCA2 in Ovarian Development and Function
A Weinberg-Shukron, M Rachmiel, P Renbaum, S Gulsuner, T Walsh, ...
New England Journal of Medicine 379 (11), 1042-1049, 2018
强制性开放获取政策： US National Institutes of Health
Genetic predisposition to breast cancer due to mutations other than BRCA1 and BRCA2 founder alleles among Ashkenazi Jewish women
T Walsh, JB Mandell, BM Norquist, S Casadei, S Gulsuner, MK Lee, ...
JAMA oncology 3 (12), 1647-1653, 2017
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Germline variants drive myelodysplastic syndrome in young adults
S Feurstein, JE Churpek, T Walsh, S Keel, M Hakkarainen, T Schroeder, ...
Leukemia 35 (8), 2439-2444, 2021
强制性开放获取政策： US National Institutes of Health, Federal Ministry of Education and Research …
Reprogramming identifies functionally distinct stages of clonal evolution in myelodysplastic syndromes
J Hsu, A Reilly, BJ Hayes, CA Clough, EQ Konnick, B Torok-Storb, ...
Blood, The Journal of the American Society of Hematology 134 (2), 186-198, 2019
强制性开放获取政策： US National Institutes of Health
Formation of Chimeric Genes by Copy-Number Variation as a Mutational Mechanism in Schizophrenia
C Rippey, T Walsh, S Gulsuner, M Brodsky, AS Nord, M Gasperini, ...
American Journal of Human Genetics 93 (4), 697–710, 2013
强制性开放获取政策： US National Institutes of Health, Wellcome Trust
Bone marrow failure unresponsive to bone marrow transplant is caused by mutations in thrombopoietin
A Seo, M Ben-Harosh, M Sirin, J Stein, O Dgany, J Kaplelushnik, ...
Blood, The Journal of the American Society of Hematology 130 (7), 875-880, 2017
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
Inherited thrombocytopenia associated with mutation of UDP-galactose-4-epimerase (GALE)
A Seo, S Gulsuner, S Pierce, M Ben-Harosh, H Shalev, T Walsh, ...
Human molecular genetics 28 (1), 133-142, 2019
强制性开放获取政策： US National Institutes of Health
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