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Kaymakcalan, Hande
65  results:
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1

Eighth case of Li‐Campeau syndrome in a Turkish patient cau..:

Edizadeh, Masoud ; Kaymakcalan, Hande ; Valilou, Saeed Farajzadeh.
American Journal of Medical Genetics Part A.  191 (2023)  5 - p. 1465-1469 , 2023
Link: https://doi.org/10.1002/..
 
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2

Mutation spectrum of congenital heart disease in a consangu..:

Dong, Weilai ; Kaymakcalan, Hande ; Jin, Sheng Chih...
Molecular Genetics & Genomic Medicine.  10 (2022)  6 - p. , 2022
Link: https://doi.org/10.1002/..
 
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3

Prevalence and clinical/molecular characteristics of PTEN m..:

Kaymakcalan, Hande ; Kaya, İlyas ; Cevher Binici, Nagihan...
Molecular Genetics & Genomic Medicine.  9 (2021)  8 - p. , 2021
Link: https://doi.org/10.1002/..
 
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4

1q21.1 Deletions and Duplications in 2 Siblings with Psychi..:

Kaymakçalan, Hande ; Li, Peining
The Indian Journal of Pediatrics.  86 (2019)  11 - p. 1068-1068 , 2019
Link: https://doi.org/10.1007/..
 
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5

Biallelic loss of human CTNNA2, encoding αN-catenin, leads ..:

Schaffer, Ashleigh E. ; Breuss, Martin W. ; Caglayan, Ahmet Okay...
Nature Genetics.  50 (2018)  8 - p. 1093-1101 , 2018
Link: https://doi.org/10.1038/..
 
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6

Novel compound heterozygous mutations in GPT2 linked to mic..:

Kaymakcalan, Hande ; Yarman, Yanki ; Goc, Nukte...
American Journal of Medical Genetics Part A.  176 (2017)  2 - p. 421-425 , 2017
Link: https://doi.org/10.1002/..
 
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7

NGLY1 mutation causes neuromotor impairment, intellectual d..:

Caglayan, Ahmet Okay ; Comu, Sinan ; Baranoski, Jacob F....
European Journal of Medical Genetics.  58 (2015)  1 - p. 39-43 , 2015
Link: https://doi.org/10.1016/..
 
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8

Changes in peanut allergy prevalence in different ethnic gr..:

Fox, Adam T. ; Kaymakcalan, Hande ; Perkin, Michael..
Journal of Allergy and Clinical Immunology.  135 (2015)  2 - p. 580-582 , 2015
Link: https://doi.org/10.1016/..
 
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9

Brain Malformations Associated With Knobloch Syndrome—Revie..:

Caglayan, Ahmet Okay ; Baranoski, Jacob F. ; Aktar, Fesih...
Pediatric Neurology.  51 (2014)  6 - p. 806-813.e8 , 2014
Link: https://doi.org/10.1016/..
 
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10

Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations i..:

Clark, Victoria E. ; Erson-Omay, E. Zeynep ; Serin, Akdes...
Science.  339 (2013)  6123 - p. 1077-1080 , 2013
Link: http://dx.doi.org/10.112..
 
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11

Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations i..:

Clark, Victoria E. ; Erson-Omay, E. Zeynep ; Serin, Akdes...
Science.  339 (2013)  6123 - p. 1077-1080 , 2013
Link: https://www.jstor.org/st..
 
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12

Genomic Analysis of Non-NF2Meningiomas Reveals Mutations in..:

Clark, Victoria E. ; Erson-Omay, E. Zeynep ; Serin, Akdes...
Science.  339 (2013)  6123 - p. 1077-1080 , 2013
Link: https://doi.org/10.1126/..
 
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13

Prenatal Health, Educational Attainment, and Intergeneratio..:

Härkönen, Juho ; Kaymakçalan, Hande ; Mäki, Pirjo.
Demography.  49 (2012)  2 - p. 525-552 , 2012
Link: https://www.jstor.org/st..
 
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14

Recessive LAMC3 mutations cause malformations of occipital ..:

Barak, Tanyeri ; Kwan, Kenneth Y ; Louvi, Angeliki...
Nature Genetics.  43 (2011)  6 - p. 590-594 , 2011
Link: https://doi.org/10.1038/..
 
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15

Whole-exome sequencing identifies recessive WDR62 mutations..:

Bilgüvar, Kaya ; Öztürk, Ali Kemal ; Louvi, Angeliki...
Nature.  467 (2010)  7312 - p. 207-210 , 2010
Link: https://doi.org/10.1038/..
 
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