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VALIDITY EXPIRED
personal data approved: 2021. XII. 09.
Personal data
name Márton Doleschall
name of institution
doctoral school
SE Károly Rácz Doctoral School of Clinical Medicine (Academic staff member)
SE Doctoral School of University Semmelweis (Academic staff member)
the share of work in the different doctoral schools. SE Doctoral School of University Semmelweis 100%
accreditation statement submitted to: Semmelweis University, Budapest
Contact details
E-mail address doleschall.martonmed.semmelweis-univ.hu
phone number +36 1 459-1500/56506
mobile phone number +36 30 536-4111
own web page
Academic title
scientific degree, title Ph.D.
year degree was obtained 2007
discipline to which degree belongs veterinary sciences
institution granting the degree Szent Istvan University
Employment
2013 - Semmelweis University, Budapest
other (not specified) (tudományos főmunkatárs)
Thesis topic supervisor
number of doctoral students supervised until now
number of students who fulfilled course requirements
students who obtained their degrees:
(50%) Zoltán Herold PhD 2021  DSCM-SE

  Thesis topic proposals
Research
research area genetics, bioinformatics, endocrinolgy
research field in which current research is conducted general health sciences
clinical medicine
Publications
2021

Herold Zoltan, Doleschall Marton, Somogyi Aniko: Role and function of granin proteins in diabetes mellitus, WORLD JOURNAL OF DIABETES 12: (7) pp. 1081-1092.
type of document: Journal paper/Review paper
language: English
URL 
2020

Herold Zoltan, Herold Magdolna, Rosta Klara, Doleschall Marton, Somogyi Aniko: Lower serum chromogranin B level is associated with type 1 diabetes and with type 2 diabetes patients with intensive conservative insulin treatment, DIABETOLOGY AND METABOLIC SYNDROME 12: (1) 61
type of document:
number of independent citations: 3
language: English
URL 
2020

Herold Zoltan, Herold Magdolna, Nagy Peter, Patocs Attila, Doleschall Marton, Somogyi Aniko: Serum chromogranin A level continuously rises with the progression of type 1 diabetes, and indicates the presence of both enterochromaffin‐like cell hyperplasia and autoimmune gastritis, JOURNAL OF DIABETES INVESTIGATION 11: (4) pp. 865-873.
type of document: Journal paper/Article
number of independent citations: 5
language: English
URL 
2018

Doleschall Márton, Török Dóra, Mészáros Katalin, Luczay Andrea, Halász Zita, Németh Krisztina, Szücs Nikolette, Kiss Róbert, Tőke Judit, Sólyom János, Fekete György, Patócs Attila, Igaz Péter, Tóth Miklós: Szteroid-21-hidroxiláz-deficientia, a congenitalis adrenalis hyperplasia leggyakoribb oka [Steroid 21-hydroxylase deficiency, the most frequent cause of congenital adrenal hyperplasia], ORVOSI HETILAP 159: (7) pp. 269-277.
type of document: Journal paper/Review paper
number of independent citations: 3
language: Hungarian
URL 
2017

Doleschall M, Luczay A, Koncz K, Hadzsiev K, Erhardt E, Szilagyi A, Doleschall Z, Nemeth K, Torok D, Prohaszka Z, Gereben B, Fekete G, Glaz E, Igaz P, Korbonits M, Toth M, Racz K, Patocs A: A unique haplotype of RCCX copy number variation, EUROPEAN JOURNAL OF HUMAN GENETICS 25: (6) pp. 702-710.
type of document: Journal paper/Article
number of independent citations: 3
language: English
URL 
2014

Doleschall M, Szabo JA, Pazmandi J, Szilagyi A, Koncz K, Farkas H, Toth M, Igaz P, Glaz E, Prohaszka Z, Korbonits M, Racz K, Fust G, Patocs A: Common Genetic Variants of the Human Steroid 21-Hydroxylase Gene (CYP21A2) Are Related to Differences in Circulating Hormone Levels., PLOS ONE 9: (9) e107244
type of document: Journal paper/Article
number of independent citations: 7
language: English
URL 
2013

Banlaki Z, Szabo JA, Szilagyi A, Patocs A, Prohaszka Z, Fust G, Doleschall M: Intraspecific Evolution of Human RCCX Copy Number Variation Traced by Haplotypes of the CYP21A2 Gene, GENOME BIOLOGY AND EVOLUTION 5: (1) pp. 98-112.
type of document: Journal paper/Article
number of independent citations: 6
language: English
URL 
2013

Szabo JA, Szilagyi A, Doleschall Z, Patocs A, Farkas H, Prohaszka Z, Racz K, Fust G, Doleschall M: Both Positive and Negative Selection Pressures Contribute to the Polymorphism Pattern of the Duplicated Human CYP21A2 Gene., PLOS ONE 8: (11) e81977
type of document: Journal paper/Article
number of independent citations: 6
language: English
URL 
2006

Zeöld A, Doleschall M, Haffner C, Capelo L, Menyhért J, Liposits Z, da Silva WS, Bianco AC, Kacskovics I, Fekete C, Gereben B: Characterization of the Nuclear Factor-κB Responsiveness of the Human dio2 Gene, ENDOCRINOLOGY 147: (9) pp. 4419-4429.
type of document: Journal paper/Article
number of independent citations: 36
language: English
URL 
2004

Fekete C, Gereben B, Doleschall M, Harney JW, Dora JM, Bianco AC, Sarkar S, Liposits Z, Rand W, Emerson C, Kacskovics I, Larsen PR, Lechan RM: Lipopolysaccharide induces type 2 iodothyronine deiodinase in the mediobasal hypothalamus: Implications for the nonthyroidal illness syndrome, ENDOCRINOLOGY 145: (4) pp. 1649-1655.
type of document: Journal paper/Article
number of independent citations: 108
language: English
URL 
Number of independent citations to these publications:177 
Scientometric data
list of publications and citations
number of scientific publications that meet accreditation criteria:
35
number of scientific publications:
35
monographs and professional books:
0
monographs/books in which chapters/sections were contributed:
0 
number of independent citations to scientific publications and creative works:
352


2024. IV. 17.
ODT ülés
Az ODT következő ülésére 2024. június 14-én, pénteken 10.00 órakor kerül sor a Semmelweis Egyetem Szenátusi termében (Bp. Üllői út 26. I. emelet).

 
All rights reserved © 2007, Hungarian Doctoral Council. Doctoral Council registration number at commissioner for data protection: 02003/0001. Program version: 2.2358 ( 2017. X. 31. )