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N

Niels de Wind

leiden university - excl lumc
H指数:44
被引数:5,915

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Discordant Staining Patterns and Microsatellite Results in Tumors of MSH6 Pathogenic Variant Carriers
MODERN PATHOLOGY
IF5.5
2023-09-016
OAAI
van der Werf-'t, Anne-Sophie; Terlouw, Diantha; Tops, Carli M.; van Kan, Merel S.; van Hest, Liselotte P.; Gille, Hans J. P.; Duijkers, Floor A. M.; Wagner, Anja; Eikenboom, Ellis L.; Letteboer, Tom G. W.; de Jong, Mirjam M.; Broeke, Sanne W. Bajwa-ten; Bleeker, Fonnet E.; Garcia, Encarna B. Gomez; de Wind, Niels; van Wezel, J. Tom; Morreau, Hans; Suerink, Manon; Nielsen, Maartje
Unexpected moves: a conformational change in MutSα enables high-affinity DNA mismatch binding
NUCLEIC ACIDS RESEARCH
IF13.1
2023-01-307
OAAI
Bruekner, Susanne R.; Pieters, Wietske; Fish, Alexander; Liaci, A. Manuel; Scheffers, Serge; Rayner, Emily; Kaldenbach, Daphne; Drost, Lisa; Dekker, Marleen; van Hees-Stuivenberg, Sandrine; Delzenne-Goette, Elly; de Konink, Charlotte; Houlleberghs, Hellen; Dubbink, Hendrikus Jan; AlSaegh, Abeer; de Wind, Niels; Forster, Friedrich; te Riele, Hein; Sixma, Titia K.
CNOT6: A Novel Regulator of DNA Mismatch Repair

CNOT6: 一种新的DNA错配修复调节剂

CELLS
IF5.2
2022-02-027
OAAI
Song, Peng; Liu, Shaojun; Liu, Dekang; Keijzers, Guido; Bakula, Daniela; Duan, Shunlei; de Wind, Niels; Ye, Zilu; Vakhrushev, Sergey Y.; Scheibye-Knudsen, Morten; Rasmussen, Lene Juel
A functional assay-based procedure to classify mismatch repair gene variants in Lynch syndrome

一种基于功能分析的程序，用于对Lynch综合征中的错配修复基因变异进行分类

GENETICS IN MEDICINE
IF6.2
2019-07-0132
OAAI
Drost, Mark; Tiersma, Yvonne; Thompson, Bryony A.; Frederiksen, Jane H.; Keijzers, Guido; Glubb, Dylan; Kathe, Scott; Osinga, Jan; Westers, Helga; Pappas, Lisa; Boucher, Kenneth M.; Molenkamp, Siska; Zonneveld, Jose B.; van Asperen, Christi J.; Goldgar, David E.; Wallace, Susan S.; Sijmons, Rolf H.; Spurdle, Amanda B.; Rasmussen, Lene J.; Greenblatt, Marc S.; de Wind, Niels; Tavtigian, Sean V.
Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency Syndrome

疑似Lynch综合征或体质错配修复缺陷综合征的大量先证者中PMS2的综合突变分析

HUMAN MUTATION
IF3.7
2016-08-2148
OAAI
van der Klift, Heleen M.; Mensenkamp, Arjen R.; Drost, Mark; Bik, Elsa C.; Vos, Yvonne J.; Gille, Hans J. J. P.; Redeker, Bert E. J. W.; Tiersma, Yvonne; Zonneveld, Jose B. M.; Garcia, Encarna Gomez; Letteboer, Tom G. W.; Olderode-Berends, Maran J. W.; van Hest, Liselotte P.; van Os, Theo A.; Verhoef, Senno; Wagner, Anja; van Asperen, Christi J.; ten Broeke, Sanne W.; Hes, Frederik J.; de Wind, Niels; Nielsen, Maartje; Devilee, Peter; Ligtenberg, Marjolijn J. L.; Wijnen, Juul T.; Tops, Carli M. J.

研究方向

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J
Jacob G. Jansen
H 指数:27论文数:78被引数:1,929
A
Anastasia Tsaalbi‐Shtylik
H 指数:13论文数:44被引数:755
M
Mark Drost
H 指数:12论文数:74被引数:570
L
Lene Juel Rasmussen
H 指数:50论文数:244被引数:7,920
R
Robert M.W. Hofstra
H 指数:80论文数:439被引数:2.2万
A
Amanda B. Spurdle
H 指数:95论文数:815被引数:4.0万
H
Heinz Jacobs
H 指数:41论文数:126被引数:6,223
G
Giel Hendriks
H 指数:27论文数:98被引数:2,308
L
Leon H.F. Mullenders
H 指数:56论文数:287被引数:1.2万
S
Sean V. Tavtigian
H 指数:70论文数:274被引数:3.8万