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Fulya Taylan

About Fulya Taylan

Fulya Taylan, With an exceptional h-index of 20 and a recent h-index of 18 (since 2020), a distinguished researcher at Karolinska Institutet, specializes in the field of Genetics, Cancer Genetics, Genomics, Rare Diseases, Childhood Cancer Predisposition.

His recent articles reflect a diverse array of research interests and contributions to the field:

Uncommon variants in FLG2 and NOD2 are associated with atopic dermatitis in the Ethiopian population

Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors—a nationwide, prospective Swedish study

Rare coding variants in NOX4 link high ROS levels to psoriatic arthritis mutilans

Diagnostic yield from a nationwide implementation of precision medicine for all children with cancer

813 Rare coding variants in NOX4 link high superoxide levels to psoriatic arthritis mutilans

International Undiagnosed Diseases Programs (UDPs): components and outcomes

LB1728 Searching for new candidate genes associated with atopic dermatitis in Ethiopian families

Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation

Fulya Taylan Information

University

Position

Laboratory coordinator, Karolinska University Hospital

Citations(all)

1153

Citations(since 2020)

865

Cited By

613

hIndex(all)

20

hIndex(since 2020)

18

i10Index(all)

32

i10Index(since 2020)

30

Email

University Profile Page

Google Scholar

Fulya Taylan Skills & Research Interests

Genetics

Cancer Genetics

Genomics

Rare Diseases

Childhood Cancer Predisposition

Top articles of Fulya Taylan

Uncommon variants in FLG2 and NOD2 are associated with atopic dermatitis in the Ethiopian population

JID Innovations

2024/4/29

Fulya Taylan
Fulya Taylan

H-Index: 15

Maria Bradley
Maria Bradley

H-Index: 17

Diagnostic yield and clinical impact of germline sequencing in children with CNS and extracranial solid tumors—a nationwide, prospective Swedish study

The Lancet Regional Health–Europe

2024/4/1

Bianca Tesi
Bianca Tesi

H-Index: 14

Frida Abel
Frida Abel

H-Index: 10

Anna Rosén
Anna Rosén

H-Index: 17

Fredrik Mertens
Fredrik Mertens

H-Index: 39

Gustaf Ljungman
Gustaf Ljungman

H-Index: 23

David Gisselsson
David Gisselsson

H-Index: 25

Fulya Taylan
Fulya Taylan

H-Index: 15

Ann Nordgren
Ann Nordgren

H-Index: 30

Rare coding variants in NOX4 link high ROS levels to psoriatic arthritis mutilans

EMBO Molecular Medicine

2024/2/20

Xiaowei Zheng
Xiaowei Zheng

H-Index: 5

Fulya Taylan
Fulya Taylan

H-Index: 15

Diagnostic yield from a nationwide implementation of precision medicine for all children with cancer

JCO Precision Oncology

2023/6

Frida Abel
Frida Abel

H-Index: 10

Bianca Tesi
Bianca Tesi

H-Index: 14

Fulya Taylan
Fulya Taylan

H-Index: 15

Khurram Maqbool
Khurram Maqbool

H-Index: 8

Fredrik Mertens
Fredrik Mertens

H-Index: 39

Ann Nordgren
Ann Nordgren

H-Index: 30

Gustaf Ljungman
Gustaf Ljungman

H-Index: 23

David Gisselsson
David Gisselsson

H-Index: 25

813 Rare coding variants in NOX4 link high superoxide levels to psoriatic arthritis mutilans

Journal of Investigative Dermatology

2023/5/1

International Undiagnosed Diseases Programs (UDPs): components and outcomes

2023/11/9

Fulya Taylan
Fulya Taylan

H-Index: 15

Ann Nordgren
Ann Nordgren

H-Index: 30

LB1728 Searching for new candidate genes associated with atopic dermatitis in Ethiopian families

Journal of Investigative Dermatology

2023/9/1

Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation

Frontiers in Medicine

2023/7/28

Fulya Taylan
Fulya Taylan

H-Index: 15

Bianca Tesi
Bianca Tesi

H-Index: 14

Ann Nordgren
Ann Nordgren

H-Index: 30

Maria Cerminara 1, Giovanni Spirito2, Livia Pisciotta 1, 3, Margherita Squillario4, Martina Servetti 1, 4, Maria Teresa Divizia 4, Margherita Lerone4, Bianca Berloco 5, Silvia …

Developmental Delay and Intellectual Disability

2022/10/19

Chen Li
Chen Li

H-Index: 6

Fulya Taylan
Fulya Taylan

H-Index: 15

Mosaic deletions of known genes explain skeletal dysplasias with high and low bone mass

Journal of Bone and Mineral Research Plus

2022/8/1

Fulya Taylan
Fulya Taylan

H-Index: 15

Ecosystem models based on artificial intelligence

2022/6/13

Claes Strannegård
Claes Strannegård

H-Index: 7

Petter Mostad
Petter Mostad

H-Index: 14

Simon Olsson
Simon Olsson

H-Index: 15

Heather Reese
Heather Reese

H-Index: 14

Fulya Taylan
Fulya Taylan

H-Index: 15

Ann Nordgren
Ann Nordgren

H-Index: 30

A somatic UBA2 variant preceded ETV6-RUNX1 in the concordant BCP-ALL of monozygotic twins

Blood Advances

2022/4/12

Vasilios Zachariadis
Vasilios Zachariadis

H-Index: 11

Fulya Taylan
Fulya Taylan

H-Index: 15

Ann Nordgren
Ann Nordgren

H-Index: 30

Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants

Molecular Genetics & Genomic Medicine

2022/4

Anna Lindstrand
Anna Lindstrand

H-Index: 23

Bianca Tesi
Bianca Tesi

H-Index: 14

Fulya Taylan
Fulya Taylan

H-Index: 15

Ann Nordgren
Ann Nordgren

H-Index: 30

A complex DICER1 syndrome phenotype associated with a germline pathogenic variant affecting the RNase IIIa domain of DICER1

Journal of Medical Genetics

2022/2/1

Fulya Taylan
Fulya Taylan

H-Index: 15

Ann Nordgren
Ann Nordgren

H-Index: 30

A missense mutation converts the Na+, K+-ATPase into an ion channel and causes therapy-resistant epilepsy

Journal of Biological Chemistry

2021/12/1

Fulya Taylan
Fulya Taylan

H-Index: 15

Maria Lindskog
Maria Lindskog

H-Index: 17

Magnus Andersson
Magnus Andersson

H-Index: 7

Anna Lindstrand
Anna Lindstrand

H-Index: 23

Anita Aperia
Anita Aperia

H-Index: 30

High diagnostic yield in skeletal ciliopathies using massively parallel genome sequencing, structural variant screening and RNA analyses

Journal of Human Genetics

2021/10

Atsuhiko Handa
Atsuhiko Handa

H-Index: 6

Hironobu Hyodo
Hironobu Hyodo

H-Index: 10

Måns Magnusson
Måns Magnusson

H-Index: 29

Daniel Nilsson
Daniel Nilsson

H-Index: 8

Fulya Taylan
Fulya Taylan

H-Index: 15

Ann Nordgren
Ann Nordgren

H-Index: 30

Anna Lindstrand
Anna Lindstrand

H-Index: 23

Giedre Grigelioniene
Giedre Grigelioniene

H-Index: 20

Oligogenic inheritance of monoallelic TRIP11, FKBP10, NEK1, TBX5, and NBAS variants leading to a phenotype similar to odontochondrodysplasia

Frontiers in Genetics

2021/6/2

Fulya Taylan
Fulya Taylan

H-Index: 15

Chromatin interactions in differentiating keratinocytes reveal novel atopic dermatitis–and psoriasis-associated genes

Journal of Allergy and Clinical Immunology

2021/5/1

Rapolas Spalinskas
Rapolas Spalinskas

H-Index: 6

Ankit Srivastava
Ankit Srivastava

H-Index: 3

Andor Pivarcsi
Andor Pivarcsi

H-Index: 36

Fulya Taylan
Fulya Taylan

H-Index: 15

Maria Bradley
Maria Bradley

H-Index: 17

Novel form of rhizomelic skeletal dysplasia associated with a homozygous variant in GNPNAT1

Journal of Medical Genetics

2021/5/1

Noor Ul Ain
Noor Ul Ain

H-Index: 3

Fulya Taylan
Fulya Taylan

H-Index: 15

Sadaf Naz
Sadaf Naz

H-Index: 16

Al‐Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2‐Related Disorders

Journal of Bone and Mineral Research

2020/12/1

Fulya Taylan
Fulya Taylan

H-Index: 15

Koray Boduroglu
Koray Boduroglu

H-Index: 17

Raymond J Louie
Raymond J Louie

H-Index: 12

Peer Arts
Peer Arts

H-Index: 14

Nikos Papadogiannakis
Nikos Papadogiannakis

H-Index: 21

Anna Lindstrand
Anna Lindstrand

H-Index: 23

Ann Nordgren
Ann Nordgren

H-Index: 30

Giedre Grigelioniene
Giedre Grigelioniene

H-Index: 20

See List of Professors in Fulya Taylan University(Karolinska Institutet)