Genomic Markers of Ovarian Reserve

Por Wood, Michelle A., Rajkovic, Aleksandar
Publicado em 2013

Reproductive aging and MCM8/9

Por Yatsenko, Svetlana A., Rajkovic, Aleksandar
Publicado no Oncotarget (2015)

Germ Cell-Specific Transcriptional Regulator Sohlh2 Is Essential for Early Mouse Folliculogenesis and Oocyte-Specific Gene Expression

Por Choi, Youngsok, Yuan, Daniel, Rajkovic, Aleksandar
Publicado em 2008

Novel Mutation in the PKHD1 Gene Diagnosed Prenatally in a Fetus with Autosomal Recessive Polycystic Kidney Disease

Por Thakur, Pankaj, Speer, Paul, Rajkovic, Aleksandar
Publicado em 2014

Generation of a germ cell-specific mouse transgenic CHERRY reporter, Sohlh1-mCherryFlag

Por Suzuki, Hitomi, Dann, Christina Tenenhaus, Rajkovic, Aleksandar
Publicado em 2012

Detection of novel copy number variants in uterine leiomyomas using high-resolution SNP arrays

Por Bowden, Wayne, Skorupski, Josh, Kovanci, Ertug, Rajkovic, Aleksandar
Publicado em 2009

Lim Homeobox Gene, Lhx8, Is Essential for Mouse Oocyte Differentiation and Survival

Por Choi, Youngsok, Ballow, Daniel J., Xin, Yun, Rajkovic, Aleksandar
Publicado em 2008

Mouse HORMAD1 Is a Meiosis I Checkpoint Protein That Modulates DNA Double-Strand Break Repair During Female Meiosis

Por Shin, Yong-Hyun, McGuire, Megan M., Rajkovic, Aleksandar
Publicado em 2013

EXPRESSION AND LOCALIZATION OF THE NOVEL AND HIGHLY-CONSERVED GAMETOCYTE SPECIFIC FACTOR 1 (GTSF1) DURING OOGENESIS AND SPERMATOGENESIS

Por Krotz, Stephan P., Ballow, Daniel J., Choi, Youngsok, Rajkovic, Aleksandar
Publicado no Fertil Steril (2008)

Recent advances of genomic testing in perinatal medicine

Por Peters, David G., Yatsenko, Svetlana A., Surti, Urvashi, Rajkovic, Aleksandar
Publicado no Semin Perinatol (2014)

Premature ovarian failure in nobox-deficient mice is caused by defects in somatic cell invasion and germ cell cyst breakdown

Por Lechowska, Agnieszka, Bilinski, Szczepan, Choi, Youngsok, Shin, Yonghyun, Kloc, Malgorzata, Rajkovic, Aleksandar
Publicado em 2011

Prenatal diagnosis of trisomy 6q25.3-qter and monosomy 10q26.12-qter by array CGH in a fetus with an apparently normal karyotype

Por Marinescu, Ponnila S, Saller, Devereux N, Parks, W Tony, Yatsenko, Svetlana A, Rajkovic, Aleksandar
Publicado no Clin Case Rep (2015)

Maternal Cell free DNA based screening for fetal microdeletion and the importance of careful diagnostic follow up

Por Yatsenko, Svetlana A., Peters, David, Saller, Devereux, Chu, Tianjiao, Clemens, Michelle, Rajkovic, Aleksandar
Publicado no Genet Med (2015)

NOBOX Homeobox Mutation Causes Premature Ovarian Failure

Por Qin, Yingying , Choi, Youngsok , Zhao, Han , Simpson, Joe Leigh , Chen, Zi-Jiang , Rajkovic, Aleksandar 
Publicado em 2007

LHX8 Mutation Analysis in Premature Ovarian Failure

Por Qin, Yingying, Zhao, Han, Kovanci, Ertug, Simpson, Joe Leigh, Chen, Zi-Jiang, Rajkovic, Aleksandar
Publicado em 2007

GDF9 Mutation Analyses in 100 Chinese Women with Premature Ovarian Failure (POF)

Por Zhao, Han, Qin, Yingying, Kovanci, Ertug, Simpson, Joe Leigh, Rajkovic, Aleksandar, Chen, Zi-Jiang
Publicado em 2007

Mutation Analysis of NANOS3 in 80 Chinese and 88 Caucasian Women with Premature Ovarian Failure

Por Qin, Yingying, Zhao, Han, Kovanci, Ertug, Simpson, Joe Leigh, Chen, Zi-Jiang, Rajkovic, Aleksandar
Publicado em 2007

Whole Exome Sequencing in a Random Sample of North American Women with Leiomyomas Identifies MED12 Mutations in Majority of Uterine Leiomyomas

Por McGuire, Megan M., Yatsenko, Alexander, Hoffner, Lori, Jones, Mirka, Surti, Urvashi, Rajkovic, Aleksandar
Publicado em 2012

SOHLH1 and SOHLH2 coordinate spermatogonial differentiation

Por Suzuki, Hitomi, Ahn, Hyo Won, Chu, Tianjiao, Bowden, Wayne, Gassei, Kathrin, Orwig, Kyle, Rajkovic, Aleksandar
Publicado em 2011

Med12 gain-of-function mutation causes leiomyomas and genomic instability

Por Mittal, Priya, Shin, Yong-hyun, Yatsenko, Svetlana A., Castro, Carlos A., Surti, Urvashi, Rajkovic, Aleksandar
Publicado no J Clin Invest (2015)