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Ugur Iseri, S. A.
89  results:
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1

Identification and functional characterisation of genetic v..:

Holt, R. ; Ugur Iseri, S. A. ; Wyatt, A. W....
Human Genetics.  136 (2016)  1 - p. 119-127 , 2016
Link: https://doi.org/10.1007/..
 
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2

Identifying SNP targeted pathways in partial epilepsies wit..:

Bakir-Gungor, B. ; Baykan, B. ; İseri, S. Ugur..
Epilepsy Research.  105 (2013)  1-2 - p. 92-102 , 2013
Link: https://doi.org/10.1016/..
 
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3

Macrocephaly and digital anomalies expand the phenotypic sp..:

Susgun, S ; Ben-Mahmoud, A ; Rüschendorf, F...
http://edoc.mdc-berlin.de/24024/1/24024oa.pdf.  , 2024
Link: http://edoc.mdc-berlin.d..
 
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4

Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exo..:

Feng, Y-CA ; Howrigan, DP ; Abbott, LE...
https://discovery.ucl.ac.uk/id/eprint/10081126/1/Sisodiya_AAM_FINAL_PROOF_EPI25_WES_ms_text.pdf.  , 2019
Link: https://discovery.ucl.ac..
 
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5

Identification and functional characterisation of genetic v..:

Holt, R ; Ugur Iseri, S ; Wyatt, A...
https://radar.brookes.ac.uk/radar/items/3c6d9ec4-71e7-49eb-8d3a-dc452f4035d3/1/.  , 2016
Link: https://radar.brookes.ac..
 
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6

A clinical variant in SCN1A inherited from a mosaic father ..:

Tuncer, Feyza N. ; Gormez, Zeliha ; Calik, Mustafa...
Epilepsy Research.  113 (2015)  - p. 5-10 , 2015
Link: https://doi.org/10.1016/..
 
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7

Biallelic NALCN variant detected by homozygosity mapping an..:

Susgun, S ; Yucesan, E ; Kocaturk, O...
https://aperta.ulakbim.gov.tr/record/7447.  , 2020
Link: https://aperta.ulakbim.g..
 
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8

Identifying SNP targeted pathways in partial epilepsies wit..:

Bakir-Gungor, B ; Baykan, B ; Iseri, S. Ugur..
https://aperta.ulakbim.gov.tr/record/89283.  , 2013
Link: https://aperta.ulakbim.g..
 
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9

ID 277 – The effects of BDNF Val66Met polymorphism on motor..:

Deveci, S. ; Matur, Z. ; Senturk, G....
Clinical Neurophysiology.  127 (2016)  3 - p. e53 , 2016
Link: https://doi.org/10.1016/..
 
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10

A clinical variant in SCN1A inherited from a mosaic father ..:

Tuncer, Feyza N ; Gormez, Zeliha ; Calik, Mustafa...
https://aperta.ulakbim.gov.tr/record/114350.  , 2015
Link: https://aperta.ulakbim.g..
 
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11

Applied Genomics in the Clinic:

GRIBALDO Laura ; AYGUN Sadiye Birep ; BRAND Angela...
JRC83263.  , 2013
Link: https://publications.jrc..
 
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12

Distinct gene-set burden patterns underlie common generaliz..:

Koko, Mahmoud ; Krause, Roland ; Sander, Thomas...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.ebiom.2021.103588.  , 2021
Link: https://repository.vu.lt..
 
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13

Epilepsy or neurodevelopmental disorders are associated wit..:

Khalilov, Dovlat ; Haryanyan, Garen ; Salman, Baris...
Neurocase.  28 (2022)  6 - p. 488-492 , 2022
Link: https://doi.org/10.1080/..
 
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14

The rare rs769301934 variant in NHLRC1 is a common cause of..:

Haryanyan, Garen ; Ozdemir, Ozkan ; Tutkavul, Kemal...
Journal of Human Genetics.  66 (2021)  12 - p. 1145-1151 , 2021
Link: https://doi.org/10.1038/..
 
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15

SYNE1 related cerebellar ataxia presents with variable phen..:

Yucesan, E. ; Ugur Iseri, Sibel A. ; Bilgic, B....
Neurological Sciences.  38 (2017)  12 - p. 2203-2207 , 2017
Link: https://doi.org/10.1007/..
 
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