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51. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

53. D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia

54. Bi-allelic variants in SPATA5L1 lead to intellectual disability, spastic-dystonic cerebral palsy, epilepsy, and hearing loss

55. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

56. X-linked recessive TLR7 deficiency in similar to 1% of men under 60 years old with life-threatening COVID-19

58. Overlapping 16p13.11 deletion and gain of copies variations associated with childhood onset psychosis include genes with mechanistic implications for autism associated pathways: Two case reports

60. HUMAN GENETICS: De novo mutations in congenital heart disease with neurodevelopmental and other congenital anomalies

63. Combining genomic and epidemiological data to compare the transmissibility of SARS-CoV-2 lineages

64. Biallelic frameshift variants in PHLDB1cause mild-type osteogenesis imperfecta with regressive spondylometaphyseal changes

65. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19.

66. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

67. Autoantibodies neutralizing type I IFNs are present in similar to 4% of uninfected individuals over 70 years old and account for similar to 20% of COVID-19 deaths

68. Additional file 2 of Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

69. Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM.

71. Genetic Defects in DNAH2 Underlie Male Infertility With Multiple Morphological Abnormalities of the Sperm Flagella in Humans and Mice

73. De novo mutations revealed by whole-exome sequencing are strongly associated with autism

76. Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

77. L-histidine decarboxylase and Tourette's syndrome

79. Further delineation of familial polycystic ovary syndrome (PCOS) via whole‐exome sequencing: PCOS‐related rare FBN3 and FN1 gene variants are identified.

80. ALG13 X‐linked intellectual disability: New variants, glycosylation analysis, and expanded phenotypes

82. Neuroinvasion of SARS-CoV-2 in human and mouse brain

83. The distinct genetic pattern of ALS in Turkey and novel mutations

84. Human CRY1 variants associate with attention deficit/hyperactivity disorder

85. Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy

86. Autoantibodies against type I IFNs in patients with life-threatening COVID-19

87. Correlations between genomic subgroup and clinical features in a cohort of more than 3000 meningiomas

88. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

90. Integrative Genomics Implicates Genetic Disruption of Prenatal Neurogenesis in Congenital Hydrocephalus

91. PATH-39. ASSOCIATIONS OF GENOMIC SUBGROUP WITH RECURRENCE IN LOW-GRADE MENINGIOMAS

92. Correlations between genomic subgroup and clinical features in a cohort of more than 3000 meningiomas

93. Associations of meningioma molecular subgroup and tumor recurrence

95. Biallelic BICD2variant is a novel candidate for Cohen-like syndrome

96. D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia.

99. Neuroinvasion of SARS-CoV-2 in human and mouse brain

100. Whole exome sequencing–based analysis to identify DNA damage repair deficiency as a major contributor to gliomagenesis in adult diffuse gliomas

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