A. Rajkovic

A. Rajkovic, G. Gurda, R. Bhargava, 2017, International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists.

Chromosomal instability in women with primary ovarian insufficiency

A. Rajkovic, A. Zeleznik, M. Aarabi, 2018, Human reproduction.

CHAPTER 32 – Germ Cell Failure and Ovarian Resistance: Human Genes and Disorders

A. Rajkovic, J. Simpson, 2003 .

TAF4b Regulates Oocyte-Specific Genes Essential for Meiosis

A. Rajkovic, A. Brodsky, K. Grive, 2016, PLoS genetics.

cDNA cloning and mapping of the human creatine kinase M gene to 19q13.

M. Carty, J. Nigro, A. Rajkovic, 1987, American journal of human genetics.

Transcription factor FIGLA is mutated in patients with premature ovarian failure.

A. Rajkovic, Zi-jiang Chen, Han Zhao, 2008, American journal of human genetics.

Plasma homocyst(e)ine concentrations in eclamptic and preeclamptic African women postpartum.

A. Rajkovic, M. Malinow, G. Woelk, 1999, Obstetrics and gynecology.

Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability.

U. Surti, Huaiyang Jiang, S. Basit, 2015, Journal of Clinical Investigation.

MCM9 mutations are associated with ovarian failure, short stature, and chromosomal instability.

U. Surti, Huaiyang Jiang, A. Rajkovic, 2014, American journal of human genetics.

Interstitial 10p11.23–p12.1 microdeletions associated with developmental delay, craniofacial abnormalities, and cryptorchidism

A. Rajkovic, S. Yatsenko, F. Schneck, 2014, American journal of medical genetics. Part A.

Prenatally Diagnosed 17q12 Microdeletion Syndrome with a Novel Association with Congenital Diaphragmatic Hernia

U. Surti, A. Rajkovic, N. Hendrix, 2011, Fetal Diagnosis and Therapy.

Genetics of early mammalian folliculogenesis

A. Rajkovic, Y. Choi, Y. Choi, 2006, Cellular and Molecular Life Sciences.

LHX8 Mutation Analysis in Premature Ovarian Failure

A. Rajkovic, Yingying Qin, J. Leigh, 2009 .

Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failure.

A. Rajkovic, Zi-jiang Chen, Han Zhao, 2007, Fertility and sterility.

NOBOX homeobox mutation causes premature ovarian failure.

A. Rajkovic, Zi-jiang Chen, Han Zhao, 2007, American journal of human genetics.

High‐resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X‐linked blue cone monochromacy

U. Surti, A. Rajkovic, A. Iannaccone, 2016, Clinical genetics.

Novel inactivating mutations of the DCAF17 gene in American and Turkish families cause male infertility and female subfertility in the mouse model

A. Rajkovic, D. Turkkahraman, L. D. Kotan, 2018, Clinical genetics.

Molecular cloning of a cDNA complementary to a UDP-glucose pyrophosphorylase mRNA of dictyostelium discoideum.

A. Rajkovic, B. Haribabu, B. Fishel, 1985, Developmental Biology.

A Novel Integrated Approach for Cytogenomic Evaluation of Plasma Cell Neoplasms.

S. Swerdlow, A. Rajkovic, R. Farah, 2022, The Journal of molecular diagnostics : JMD.

Identification of expressed sequence tags preferentially expressed in human placentas by in silico subtraction

A. Rajkovic, D. Miner, 2003, Prenatal diagnosis.

Familial microduplication of 17q23.1–q23.2 involving TBX4 is associated with congenital clubfoot and reduced penetrance in females

U. Surti, A. Rajkovic, S. Yatsenko, 2014, American journal of medical genetics. Part A.

Familial deletion of the HOXA gene cluster associated with Hand–Foot–Genital syndrome and phenotypic variability

A. Rajkovic, S. Yatsenko, A. Yatsenko, 2017, American journal of medical genetics. Part A.

Single-cell sequencing reveals novel cellular heterogeneity in uterine leiomyomas.

A. Rajkovic, D. Chakravarti, S. Bulun, 2022, Human reproduction.

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

U. Surti, A. Rajkovic, Priya Mittal, 2015, The Journal of clinical investigation.

The Transition from Stem Cell to Progenitor Spermatogonia and Male Fertility Requires the SHP2 Protein Tyrosine Phosphatase

A. Rajkovic, P. Lapinski, P. King, 2014, Stem cells.

Sequence and expression of testis-expressed gene 14 (Tex14): a gene encoding a protein kinase preferentially expressed during spermatogenesis.

Wei Yan, K. Burns, M. Matzuk, 2003, Gene expression patterns : GEP.

Testis formation in XX individuals resulting from novel pathogenic variants in Wilms’ tumor 1 (WT1) gene

R. Lovell-Badge, A. Rajkovic, K. McElreavey, 2020, Proceedings of the National Academy of Sciences.

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

U. Surti, A. Rajkovic, A. Yatsenko, 2012, PloS one.

Granulocyte colony-stimulating factor with or without stem cell factor extends time to premature ovarian insufficiency in female mice treated with alkylating chemotherapy.

A. Rajkovic, T. Chu, T. Krivak, 2013, Fertility and sterility.

Genomic Markers of Ovarian Reserve

A. Rajkovic, M. Wood, 2013, Seminars in Reproductive Medicine.

Pancreatic cancer risk and ABO blood group alleles: results from the pancreatic cancer cohort consortium.

Geoffrey S. Tobias, Shannon M. Lynch, A. LaCroix, 2010, Cancer research.

A genome-wide association study identifies pancreatic cancer susceptibility loci on chromosomes 13q22.1, 1q32.1 and 5p15.33

Wei Zheng, Peter Kraft, Vittorio Krogh, 2010, Nature Genetics.

CHAPTER 10 – Follicular Development: Mouse, Sheep, and Human Models

M. Matzuk, A. Rajkovic, S. Pangas, 2006 .

Vasomotor symptoms, adoption of a low-fat dietary pattern, and risk of invasive breast cancer: a secondary analysis of the Women's Health Initiative randomized controlled dietary modification trial.

R. Chlebowski, J. Ockene, M. Stefanick, 2009, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Atypical forms of incontinentia pigmenti in male individuals result from mutations of a cytosine tract in exon 10 of NEMO (IKK-gamma).

G. Courtois, A. Israël, D. Nelson, 2001, American journal of human genetics.

Genome-wide association study of age at menarche in African-American women.

Gary K. Chen, C. Carlson, E. Demerath, 2013, Human molecular genetics.

Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study.

C. Carlson, C. Kooperberg, G. Heiss, 2012, Human molecular genetics.

X-linked ADGRG2 mutation and obstructive azoospermia in a large Pakistani family

Huaiyang Jiang, S. Basit, A. Rajkovic, 2018, Scientific Reports.

X-linked TEX11 mutations, meiotic arrest, and azoospermia in infertile men.

A. Rajkovic, A. Röpke, Andrew P. Georgiadis, 2015, The New England journal of medicine.

Nobox is a homeobox-encoding gene preferentially expressed in primordial and growing oocytes

Changning Yan, Martin M. Matzuk, M. Matzuk, 2002, Mechanisms of Development.

Chromosomal causes of infertility

A. Rajkovic, S. Yatsenko, 2014 .

Genetics of human female infertility†

A. Rajkovic, S. Yatsenko, 2019, Biology of Reproduction.

Sohlh1 is essential for spermatogonial differentiation.

M. Matzuk, A. Rajkovic, M. Meistrich, 2006, Developmental biology.

Molecular Genetic Technology

A. Rajkovic, J. Kuller, 2018 .

NOBOX Deficiency Disrupts Early Folliculogenesis and Oocyte-Specific Gene Expression

Martin M Matzuk, M. Matzuk, A. Rajkovic, 2004, Science.

Recent Developments in Identifying Genetic Determinants of Premature Ovarian Failure

A. Rajkovic, A. Skillern, 2008, Sexual Development.

Loss of Cx43 in Murine Sertoli Cells Leads to Altered Prepubertal Sertoli Cell Maturation and Impairment of the Mitosis-Meiosis Switch

A. Rajkovic, O. Distl, J. Metzger, 2020, Cells.

MicroRNAs and mammalian ovarian development.

A. Rajkovic, Han Zhao, 2008, Seminars in reproductive medicine.

Med12 regulates ovarian steroidogenesis, uterine development and maternal effects in the mammalian egg †

A. Rajkovic, Priya Mittal, C. Castro, 2017, Biology of Reproduction.

Single Cell atlas of uterine myometrium and leiomyomas reveals diverse and novel cell types of non-monoclonal origin

A. Rajkovic, D. Chakravarti, S. Bulun, 2020, bioRxiv.

The Role of Mediator Complex Subunit 12 in Leiomyoma Biology

A. Rajkovic, Priya Mittal, X. Wang, 2016, Current Genetic Medicine Reports.

Ovarian Follicular Theca Cell Recruitment, Differentiation, and Impact on Fertility: 2017 Update.

A. Rajkovic, J. Richards, Y. Ren, 2018, Endocrine reviews.

Functional analysis of oocyte-expressed genes using transgenic models

M. Matzuk, A. Rajkovic, 2002, Molecular and Cellular Endocrinology.

Restricted germ cell expression of a gene encoding a novel mammalian HORMA domain-containing protein.

Wei Yan, M. Matzuk, A. Rajkovic, 2004, Gene expression patterns : GEP.

TEX14 is essential for intercellular bridges and fertility in male mice.

Julio E. Agno, R. Braun, Wei Yan, 2006, Proceedings of the National Academy of Sciences of the United States of America.

Identification of Gasz, an evolutionarily conserved gene expressed exclusively in germ cells and encoding a protein with four ankyrin repeats, a sterile-alpha motif, and a basic leucine zipper.

Wei Yan, K. Burns, M. Matzuk, 2002, Molecular endocrinology.

Biological significance of HORMA domain containing protein 1 (HORMAD1) in epithelial ovarian carcinoma.

A. Sood, A. Rajkovic, Wei Hu, 2013, Cancer letters.

Reproductive aging and MCM8/9

A. Rajkovic, S. Yatsenko, 2015, Oncotarget.

Genetic Variation and Reproductive Timing: African American Women from the Population Architecture Using Genomics and Epidemiology (PAGE) Study

C. Carlson, C. Carty, T. Matise, 2013, PloS one.

Oogenesis: Transcriptional regulators and mouse models

A. Rajkovic, K. Jagarlamudi, 2012, Molecular and Cellular Endocrinology.

Candidate genes for premature ovarian failure.

A. Rajkovic, S. Pangas, N. Suzumori, 2007, Current medicinal chemistry.

Expansion of phenotype and genotypic data in CRB2-related syndrome

A. Fulton, D. Schneidman-Duhovny, A. Rajkovic, 2016, European Journal of Human Genetics.

Prenatal whole‐exome sequencing: parental attitudes

A. Rajkovic, D. Saller, A. Althouse, 2015, Prenatal diagnosis.

Human Embryonic Expression Identifies Novel Essential Gene Candidates

A. Rajkovic, H. Cakmak, Monica Penon-Portmann, 2020 .

Copy number alterations involving 59 ACMG‐recommended secondary findings genes

U. Surti, D. Bellissimo, A. Rajkovic, 2020, Clinical genetics.

Integration of microarray analysis into the clinical diagnosis of hematological malignancies: How much can we improve cytogenetic testing?

U. Surti, S. Swerdlow, A. Rajkovic, 2015, Oncotarget.

Deletion of conserved non‐coding sequences downstream from NKX2‐1: A novel disease‐causing mechanism for benign hereditary chorea

U. Surti, A. Rajkovic, J. Locker, 2021, Molecular genetics & genomic medicine.

Lim Homeobox Gene, Lhx8, Is Essential for Mouse Oocyte Differentiation and Survival1

A. Rajkovic, D. Ballow, Yun Xin, 2008, Biology of reproduction.

Meta-analysis of loci associated with age at natural menopause in African-American women.

Gary K. Chen, Kathleen F. Kerr, Jeanette S. Andrews, 2014, Human molecular genetics.

Spermatogonial SOHLH1 nucleocytoplasmic shuttling associates with initiation of spermatogenesis in the rhesus monkey (Macaca mulatta).

A. Rajkovic, Hitomi Suzuki, T. Plant, 2014, Molecular human reproduction.

Microarray Analyses of Newborn Mouse Ovaries Lacking Nobox1

Martha L Bulyk, Yingying Qin, Michael F Berger, 2007, Biology of reproduction.

High quality RNA in semen and sperm: isolation, analysis and potential application in clinical testing.

A. Rajkovic, Andrew P. Georgiadis, A. Yatsenko, 2015, The Journal of urology.

MCM8 and MCM9 Nucleotide Variants in Women With Primary Ovarian Insufficiency

Huaiyang Jiang, M. Cocca, A. Rajkovic, 2016, The Journal of clinical endocrinology and metabolism.

Cytogenetic signatures of recurrent pregnancy losses

A. Rajkovic, J. Yanowitz, D. Saller, 2020, medRxiv.

Highly heterogeneous genomic landscape of uterine leiomyomas by whole exome sequencing and genome-wide arrays.

U. Surti, A. Sood, A. Rajkovic, 2017, Fertility and Sterility.

Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiency

A. Rajkovic, D. Toniolo, C. Barbieri, 2021, Human reproduction.

Female-to-male sex reversal associated with unique Xp21.2 deletion disrupting genomic regulatory architecture of the dosage-sensitive sex reversal region

A. Rajkovic, S. Yatsenko, S. Witchel, 2017, Journal of Medical Genetics.

The Rise and Fall of Oogonial Stem Cells Within the Historical Context of Adult Stem Cells

A. Rajkovic, S. Nayak, Y. Ren, 2016 .

Pathogenic variants in ZSWIM7 cause Primary Ovarian Insufficiency.

A. Rajkovic, Yingying Qin, A. Topaloğlu, 2022, The Journal of clinical endocrinology and metabolism.

Gene variants identified by whole-exome sequencing in 33 French women with premature ovarian insufficiency

Huaiyang Jiang, A. Rajkovic, P. Touraine, 2018, Journal of Assisted Reproduction and Genetics.

Transcription factors SOHLH1 and SOHLH2 coordinate oocyte differentiation without affecting meiosis I

A. Rajkovic, H. Ahn, Yong-hyun Shin, 2017, The Journal of clinical investigation.

Novel Inactivating Mutation of the FSH Receptor in Two Siblings of Indian Origin With Premature Ovarian Failure.

A. Rajkovic, R. Muzumdar, M. Wood-Trageser, 2015, The Journal of clinical endocrinology and metabolism.

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

M. Kloc, A. Rajkovic, Yong-hyun Shin, 2011, Journal of Assisted Reproduction and Genetics.

Beyond Down syndrome phenotype: Paternally derived isodicentric chromosome 21 with partial monosomy 21q22.3

U. Surti, A. Rajkovic, D. Saller, 2017, American journal of medical genetics. Part A.

Deletion of Gremlin-2 alters estrous cyclicity and disrupts female fertility in mice

A. Rajkovic, S. Pangas, Gregory R. Gipson, 2020, Biology of Reproduction.

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

A. Rajkovic, Wayne A. Bowden, E. Kovanci, 2009, Molecular human reproduction.

Estrogen plus progestin and breast cancer incidence and mortality in postmenopausal women.

J. Manson, R. Prentice, L. Kuller, 2010, JAMA.

Autism spectrum disorder in females with ARHGEF9 alterations and a random pattern of X chromosome inactivation.

U. Surti, D. Bellissimo, A. Rajkovic, 2019, European journal of medical genetics.

Screening for autosomal recessive and X-linked conditions during pregnancy and preconception: a practice resource of the American College of Medical Genetics and Genomics (ACMG)

N. Leach, A. Rajkovic, T. Sparks, 2021, Genetics in Medicine.

Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure.

A. Rajkovic, H. Ahn, Megan M. McGuire, 2011, Fertility and sterility.

A Systematic Mapping Approach of 16q12.2/FTO and BMI in More Than 20,000 African Americans Narrows in on the Underlying Functional Variation: Results from the Population Architecture using Genomics and Epidemiology (PAGE) Study

Dana C. Crawford, Praveen Sethupathy, Lucia A. Hindorff, 2013, PLoS genetics.

Prenatal Diagnosis of 2q32 Deletion Syndrome Characterized by Multiple Segmental Deletions and Complex Chromosomal Rearrangement Involving Chromosomes 2, 5 and 7

B. Torchia, U. Surti, A. Rajkovic, 2012, Fetal Diagnosis and Therapy.

Mutations involving the SRY-related gene SOX8 are associated with a spectrum of human reproductive anomalies

P. Validire, A. Rajkovic, E. Rajpert-De Meyts, 2018, Human molecular genetics.

Functional study of a novel missense single‐nucleotide variant of NUP107 in two daughters of Mexican origin with premature ovarian insufficiency

Huaiyang Jiang, A. Rajkovic, M. Wood-Trageser, 2018, Molecular genetics & genomic medicine.

Importance of complete phenotyping in prenatal whole exome sequencing

Huaiyang Jiang, D. Bellissimo, A. Rajkovic, 2018, Human Genetics.

Female reproductive tract has low concentration of SARS-CoV2 receptors

A. Rajkovic, J. Goad, J. Rudolph, 2020, PloS one.

A high-resolution X chromosome copy-number variation map in fertile females and women with primary ovarian insufficiency

Huaiyang Jiang, A. Rajkovic, T. Chu, 2019, Genetics in Medicine.

Characterization of the association between 8q24 and colon cancer: gene-environment exploration and meta-analysis

J. Potter, D. Duggan, Jill Muehling, 2010, BMC Cancer.

Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.

U. Surti, A. Rajkovic, L. Hoffner, 2011, Fertility and sterility.

Expression of Drosophila neoplastic tumor suppressor genes discslarge, scribble, and lethal giant larvae in the mammalian ovary.

P. Szafranski, A. Rajkovic, S. Ochsner, 2003, Gene expression patterns : GEP.

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

A. Rajkovic, Yingying Qin, J. Leigh, 2009 .

Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failure.

A. Rajkovic, Zi-jiang Chen, Han Zhao, 2007, Fertility and sterility.

Cell-cell contact and cAMP regulate the expression of a UDP glucose pyrophosphorylase gene of Dictyostelium discoideum.

A. Rajkovic, B. Haribabu, R. Dottin, 1986, Developmental biology.

Transcriptional regulation of early oogenesis: in search of masters.

A. Rajkovic, S. Pangas, 2006, Human reproduction update.

Characterization of 9p24 Risk Locus and Colorectal Adenoma and Cancer: Gene–Environment Interaction and Meta-Analysis

R. Hayes, J. Potter, D. Duggan, 2010, Cancer Epidemiology, Biomarkers & Prevention.

Characterization of 9 p 24 Risk Locus and Colorectal Adenoma and Cancer : Gene – Environment Interaction and Meta-Analysis

R. Hayes, J. Potter, D. Duggan, 2010 .

High resolution non‐invasive detection of a fetal microdeletion using the GCREM algorithm

A. Rajkovic, T. Chu, K. Bunce, 2014, Prenatal diagnosis.

Motifs of the C-terminal domain of MCM9 direct localization to sites of mitomycin-C damage for RAD51 recruitment

A. Rajkovic, M. Trakselis, Wezley C. Griffin, 2020, bioRxiv.

Lhx8 regulates primordial follicle activation and postnatal folliculogenesis

A. Rajkovic, V. Pachnis, Hitomi Suzuki, 2015, BMC Biology.

regulates primordial follicle activation and postnatal folliculogenesis.

A. Rajkovic, V. Pachnis, Hitomi Suzuki, 2015 .

LHX8 DEFICIENCY DISRUPTS EARLY FOLLICULOGENESIS AND OOCYTE-SPECIFIC GENE EXPRESSION IN THE MOUSE OVARY

A. Rajkovic, D. Ballow, H. Westphal, 2007 .

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

A. Rajkovic, W. Parks, D. Saller, 2014, Clinical case reports.

Family history of cancer and risk of pancreatic cancer: A pooled analysis from the Pancreatic Cancer Cohort Consortium (PanScan)

Geoffrey S. Tobias, Shannon M. Lynch, A. LaCroix, 2010, International journal of cancer.

Low-fat dietary pattern and lipoprotein risk factors: the Women's Health Initiative Dietary Modification Trial.

Jennifer G. Robinson, C. Kooperberg, B. Howard, 2010, The American journal of clinical nutrition.

Lhx8 regulates primordial follicle activation and postnatal folliculogenesis

A. Rajkovic, V. Pachnis, Hitomi Suzuki, 2015, BMC Biology.

Breast cancer after use of estrogen plus progestin in postmenopausal women.

J. Manson, R. Prentice, L. Kuller, 2009, The New England journal of medicine.

Characterization of NOBOX DNA Binding Specificity and Its Regulation of Gdf9 and Pou5f1 Promoters*

A. Rajkovic, Aleksandar Rajkovic, Youngsok Choi, 2006, Journal of Biological Chemistry.

Discovery of germ cell-specific transcripts by expressed sequence tag database analysis.

M. Matzuk, A. Rajkovic, M. Klysik, 2001, Fertility and sterility.

Leveraging electronic health records to identify risk factors for recurrent pregnancy loss across two medical centers: a case-control study

M. Glymour, N. Aghaeepour, M. Sirota, 2023, Research Square.

Leveraging electronic health records to identify risk factors for recurrent pregnancy loss across two medical centers: a case-control study

M. Glymour, N. Aghaeepour, M. Sirota, 2023, Research square.

Placenta percreta at 7th week of pregnancy in a woman with previous caesarean section

A. Rajkovic, J. Tanyi, L. Ayensu-Coker, 2008, Journal of obstetrics and gynaecology : the journal of the Institute of Obstetrics and Gynaecology.

Methylenetetrahydrofolate reductase 677 C --> T polymorphism, plasma folate, vitamin B(12) concentrations, and risk of preeclampsia among black African women from Zimbabwe.

R. Rozen, A. Rajkovic, M. Malinow, 2000, Molecular genetics and metabolism.

Sequence and expression of testis-expressed gene 14 (Tex14): a gene encoding a protein kinase preferentially expressed during spermatogenesis.

Wei Yan, K. Burns, M. Matzuk, 2003, Gene expression patterns : GEP.

A design thinking approach to primary ovarian insufficiency.

A. Rajkovic, L. Nelson, N. Kleinstreuer, 2017, Panminerva medica.

Mutations in SOHLH1 gene associate with nonobstructive Azoospermia

Dong Ryul Lee, A. Rajkovic, Ji-Young Kim, 2010, Human mutation.

Heterozygous TP63 pathogenic variants in isolated primary ovarian insufficiency

A. Rajkovic, S. Yatsenko, A. Berman, 2023, Journal of Assisted Reproduction and Genetics.

Preimplantation Genetic Testing

A. Rajkovic, S. Yatsenko, 2022, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics.

Preimplantation Genetic Testing

A. Rajkovic, S. Yatsenko, 2022, Emery and Rimoin's Principles and Practice of Medical Genetics and Genomics.

A spliced leader is present on a subset of mRNAs from the human parasite Schistosoma mansoni.

A. Rajkovic, F. Rottman, Richard E. Davis, 1990, Proceedings of the National Academy of Sciences of the United States of America.

Sohlh1 loss of function male and female infertility model impacts overall health beyond gonadal dysfunction in mice

A. Rajkovic, Beatriz Rodríguez-Alonso, Marta Rodríguez-Escribà, 2023, Biology of Reproduction.

Low-fat Dietary Pattern and Lipoprotein Risk Factors: the Women's Health Initiative Dietary Modification Trial 1–4

Jennifer G. Robinson, C. Kooperberg, B. Howard, 2022 .

Genome-wide association study of age at menarche in African-American women.

Gary K. Chen, Kathleen F. Kerr, C. Carlson, 2013, Human molecular genetics.

Replication of loci influencing ages at menarche and menopause in Hispanic women: the Women's Health Initiative SHARe Study.

C. Carlson, C. Kooperberg, G. Heiss, 2012, Human molecular genetics.

High‐resolution microarray analysis unravels complex Xq28 aberrations in patients and carriers affected by X‐linked blue cone monochromacy

U. Surti, A. Rajkovic, M. Wood-Trageser, 2016, Clinical genetics.

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

U. Surti, A. Rajkovic, Priya Mittal, 2015, The Journal of clinical investigation.

Supplemental Material for : Med 12 Gain-of-Function Mutation Causes Leiomyomas and Genomic Instability

U. Surti, A. Rajkovic, Priya Mittal, 2015 .

Exome sequencing reveals MCM8 mutation underlies ovarian failure and chromosomal instability.

U. Surti, Huaiyang Jiang, S. Basit, 2015, The Journal of clinical investigation.

Breast cancer after use of estrogen plus progestin in postmenopausal women.

J. Manson, R. Prentice, L. Kuller, 2009, The New England journal of medicine.

237: Microrna expression in placenta of patients with preeclampsia

Xiaolian Gao, A. Rajkovic, H. Ahn, 2008 .

Spermatogonial SOHLH1 nucleocytoplasmic shuttling associates with initiation of spermatogenesis in the rhesus monkey (Macaca mulatta).

A. Rajkovic, Hitomi Suzuki, T. Plant, 2014, Molecular human reproduction.

SOHLH1 and SOHLH2 coordinate spermatogonial differentiation.

A. Rajkovic, T. Chu, H. Ahn, 2012, Developmental biology.