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검색어 [키워드: "Mertens, Mareike"]

1

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

학술저널

issue: In The American Journal of Human Genetics 7 March 2024 111(3):509-528
Author: Agrawal, Pankaj
Armstrong Scott, Daryl
Barkoudah, Elizabeth
Bellini, Melissa
Beneteau, Claire
Bjørgo, Kathrine
Brooks, Alice
Brown, Natasha
Castle, Alison
Castro, Diana
Chorin, Odelia
Cleghorn, Mark
Clement, Emma
Coman, David
Costin, Carrie
Devriendt, Koen
Dong, Dexin
Dries, Annika
Duelund Hjortshøj, Tina
Dyment, David
Eng, Christine
Genetti, Casie
Grano, Siera
Henneman, Peter
Heron, Delphine
Hoffmann, Katrin
Hom, Jason
Du, Haowei
Iascone, Maria
Isidor, Bertrand
Järvelä, Irma E.
Jones, Julie
Keren, Boris
Koenig, Mary Kay
Kohlhase, Jürgen
Lalani, Seema
Le Caignec, Cedric
Lewis, Andi
Liu, Pengfei
Lovgren, Alysia
Lupski, James R.
Lyons, Mike
Lysy, Philippe
Manning, Melanie
Marcelis, Carlo
McLean, Scott Douglas
Mercie, Sandra
Mertens, Mareike
Molin, Arnaud
Nizon, Mathilde
Nugent, Kimberly Margaret
Öhman, Susanna
O'Leary, Melanie
Okashah Littlejohn, Rebecca
Petit, Florence
Pfundt, Rolph
Pottocki, Lorraine
Raas-Rotschild, Annick
Ranguin, Kara
Revencu, Nicole
Rosenfeld, Jill
Rhodes, Lindsay
Santos Simmaro, Fernando
Sals, Karen
Schieving, Jolanda
Schrauwen, Isabelle
Schuurs-Hoeijmakers, Janneke H.M.
Seaby, Eleanor G.
Sheffer, Ruth
Snijders Blok, Lot
Sørensen, Kristina P.
Srivastava, Siddharth
Stark, Zornitza
Stoeva, Radka
Stutterd, Chloe
Tan, Natalie B.
Mathiesen Torring, Pernille
Vanakker, Olivier
van der Laan, Liselot
Ververi, Athina
Villavicencio-Lorini, Pablo
Vincent, Marie
Wand, Dorothea
Wessels, Marja
White, Sue
Wojcik, Monica H.
Wu, Nan
Zhao, Sen
Pérez Baca, María del Rocío
Jacobs, Eva Z.
Vantomme, Lies
Leblanc, Pontus
Bogaert, Elke
Dheedene, Annelies
De Cock, Laurenz
Haghshenas, Sadegheh
Foroutan, Aidin
Levy, Michael A.
Kerkhof, Jennifer
McConkey, Haley
Chen, Chun-An
Batzir, Nurit Assia
Wang, Xia
Palomares, María
Carels, Marieke
Dermaut, Bart
Sadikovic, Bekim
Menten, Björn
Yuan, Bo
Vergult, Sarah
Callewaert, Bert
DB Label: Database : ScienceDirect

원문보기: 등재 - Web of Science (SCIE) 등재 - SCOPUS 조회 - Impact Factor (JCR)

2

Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature

학술저널

issue: American Journal of Human Genetics. 108(6)
Author: Rots, Dmitrijs
Chater-Diehl, Eric
Dingemans, Alexander JM
Goodman, Sarah J
Siu, Michelle T
Cytrynbaum, Cheryl
Choufani, Sanaa
Hoang, Ny
Walker, Susan
Awamleh, Zain
Charkow, Joshua
Meyn, Stephen
Pfundt, Rolph
Rinne, Tuula
Gardeitchik, Thatjana
de Vries, Bert BA
Deden, A Chantal
Leenders, Erika
Kwint, Michael
Stumpel, Constance TRM
Stevens, Servi JC
Vermeulen, Jeroen R
van Harssel, Jeske VT
Bosch, Danielle GM
van Gassen, Koen LI
van Binsbergen, Ellen
de Geus, Christa M
Brackel, Hein
Hempel, Maja
Lessel, Davor
Denecke, Jonas
Slavotinek, Anne
Strober, Jonathan
Crunk, Amy
Folk, Leandra
Wentzensen, Ingrid M
Yang, Hui
Zou, Fanggeng
Millan, Francisca
Person, Richard
Xie, Yili
Liu, Shuxi
Ousager, Lilian B
Larsen, Martin
Schultz-Rogers, Laura
Morava, Eva
Klee, Eric W
Berry, Ian R
Campbell, Jennifer
Lindstrom, Kristin
Pruniski, Brianna
Neumeyer, Ann M
Radley, Jessica A
Phornphutkul, Chanika
Schmidt, Berkley
Wilson, William G
Õunap, Katrin
Reinson, Karit
Pajusalu, Sander
van Haeringen, Arie
Ruivenkamp, Claudia
Cuperus, Roos
Santos-Simarro, Fernando
Palomares-Bralo, María
Pacio-Míguez, Marta
Ritter, Alyssa
Bhoj, Elizabeth
Tønne, Elin
Tveten, Kristian
Cappuccio, Gerarda
Brunetti-Pierri, Nicola
Rowe, Leah
Bunn, Jason
Saenz, Margarita
Platzer, Konrad
Mertens, Mareike
Caluseriu, Oana
Nowaczyk, Małgorzata JM
Cohn, Ronald D
Kannu, Peter
Alkhunaizi, Ebba
Chitayat, David
Scherer, Stephen W
Brunner, Han G
Vissers, Lisenka ELM
Kleefstra, Tjitske
Koolen, David A
Weksberg, Rosanna
DB Label: Database : eScholarship

원문보기: Open Access (eScholarship)

3

Genetische Tumorprädispositionssyndrome
Cancer predisposition syndromes

학술저널

issue: Die Onkologie : Organ der Deutschen Krebsgesellschaft e.V.. 28(6):534-545
Author: Mertens, Mareike
Schumann, Isabell
Stiller, Mathias
Lemke, Johannes R.
Strehlow, Vincent
Hentschel, Julia^{Aff1, IDs00761022011561_cor6}
DB Label: Database : Springer Nature Journals

원문보기: 등재 - Web of Science (SCIE)

4

Genetische Tumorprädispositionssyndrome

정기출판물

issue: Der Onkologe; 20240101, Issue: Preprints p1-12, 12p
Author: Mertens, Mareike
Schumann, Isabell
Stiller, Mathias
Lemke, Johannes R.
Strehlow, Vincent
Hentschel, Julia
DB Label: Database : Supplemental Index

원문보기: 등재 - SCOPUS 조회 - Impact Factor (JCR) 원문복사신청 - RISS

5

Cancer predisposition syndromes

학술저널

issue: ONKOLOGIE; JUN 2022, 28 6, p534-p543, 10p.
Author: Mertens, Mareike
Schumann, Isabell
Stiller, Mathias
Lemke, Johannes R.
Strehlow, Vincent
Hentschel, Julia
DB Label: Database : Science Citation Index Expanded

원문보기: 등재 - Web of Science

6

Who am I? Donor DNA in Patients after Stem Cell Transplantation

학술저널

issue: EUROPEAN JOURNAL OF HUMAN GENETICS; MAY 11 2023, 31 p593-p593, 1p. Supplement: 1
Author: Mertens, Mareike
Sadlo, Mona
Hentschel, Julia
DB Label: Database : Science Citation Index Expanded

원문보기: 등재 - Web of Science 등재 - SCOPUS 조회 - Impact Factor (JCR)

7

In depth evaluation of a 9p tetrasomy

학술저널

issue: EUROPEAN JOURNAL OF HUMAN GENETICS; APR 2022, 30 SUPPL 1, p450-p450, 1p. Supplement: 1
Author: Radtke, Maximilian
Mertens, Mareike
Schubert, Susanna
DB Label: Database : Science Citation Index Expanded

원문보기: 등재 - Web of Science 등재 - SCOPUS 조회 - Impact Factor (JCR)

1

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