Aleksandar Rajkovic (A Rajkovic)

ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 14

Top Venues

Human genetics

Clinical genetics

Molecular genetics & genomic medicine

Human reproduction (Oxford, England)

This page only lists publications with an associated author ORCID identifier.

Publications

Mona Aminbeidokhti, Jia-Hua Qu, Shweta Belur, Hakan Cakmak, Eleni Jaswa, Ruth B Lathi, Marina Sirota, Michael P Snyder, Svetlana A Yatsenko, Aleksandar Rajkovic
Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants. Human genetics (2024)
Mona Aminbeidokhti, Jia-Hua Qu, Shweta Belur, Hakan Cakmak, Eleni Jaswa, Ruth B Lathi, Marina Sirota, Michael P Snyder, Svetlana A Yatsenko, Aleksandar Rajkovic
Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants. Human genetics (2024)
Mona Aminbeidokhti, Jia-Hua Qu, Shweta Belur, Hakan Cakmak, Eleni Jaswa, Ruth B Lathi, Marina Sirota, Michael P Snyder, Svetlana A Yatsenko, Aleksandar Rajkovic
Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants. Human genetics 143 (2) (2024)
Mona Aminbeidokhti, Jia-Hua Qu, Shweta Belur, Hakan Cakmak, Eleni Jaswa, Ruth B Lathi, Marina Sirota, Michael P Snyder, Svetlana A Yatsenko, Aleksandar Rajkovic
Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants. Human genetics (2024)
Mona Aminbeidokhti, Jia-Hua Qu, Shweta Belur, Hakan Cakmak, Eleni Jaswa, Ruth B Lathi, Marina Sirota, Michael P Snyder, Svetlana A Yatsenko, Aleksandar Rajkovic
Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants. Human genetics 143 (2) (2024)
Mona Aminbeidokhti, Jia-Hua Qu, Shweta Belur, Hakan Cakmak, Eleni Jaswa, Ruth B Lathi, Marina Sirota, Michael P Snyder, Svetlana A Yatsenko, Aleksandar Rajkovic
Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants. Human genetics (2024)
Mona Aminbeidokhti, Jia-Hua Qu, Shweta Belur, Hakan Cakmak, Eleni Jaswa, Ruth B Lathi, Marina Sirota, Michael P Snyder, Svetlana A Yatsenko, Aleksandar Rajkovic
Miscarriage risk assessment: a bioinformatic approach to identifying candidate lethal genes and variants. Human genetics 143 (2) (2024)
Mona Aminbeidokhti, Jia-Hua Qu, Shweta Belur, Hakan Cakmak, Eleni Jaswa, Ruth B Lathi, Marina Sirota, Michael P Snyder, Svetlana A Yatsenko, Aleksandar Rajkovic
Preconception Genetic Carrier Screening for Miscarriage Risk Assessment: A Bioinformatic Approach to Identifying Candidate Lethal Genes and Variants. medRxiv : the preprint server for health sciences (2023)
Jyoti Goad, Joshua Rudolph, Mehrdad Zandigohar, Matthew Tae, Yang Dai, Jian-Jun Wei, Serdar E Bulun, Debabrata Chakravarti, Aleksandar Rajkovic
Single-cell sequencing reveals novel cellular heterogeneity in uterine leiomyomas. Human reproduction (Oxford, England) 37 (10) (2022)
Svetlana A Yatsenko, Fatih Gurbuz, Ali Kemal Topaloglu, Andrea J Berman, Pierre-Marie Martin, Marta Rodrigue-Escribà, Yingying Qin, Aleksandar Rajkovic
Pathogenic Variants in ZSWIM7 Cause Primary Ovarian Insufficiency. The Journal of clinical endocrinology and metabolism 107 (6) (2022)
Svetlana A Yatsenko, Mahmoud Aarabi, Jie Hu, Urvashi Surti, Damara Ortiz, Suneeta Madan-Khetarpal, Devereux N Saller, Daniel Bellissimo, Aleksandar Rajkovic
Copy number alterations involving 59 ACMG-recommended secondary findings genes. Clinical genetics 98 (6) (2020)
A C Zielen, M J Khan, N Pollock, H Jiang, J Ahmed, R Nazli, M Jabeen, A Yatsenko, Aleksandar Rajkovic
A novel homozygous frame-shift variant in the LHCGR gene is associated with primary ovarian insufficiency in a Pakistani family. Clinical genetics 94 (3-4) (2018)
F Gurbuz, S Desai, F Diao, D Turkkahraman, F Wranitz, M Wood-Trageser, Y-H Shin, L D Kotan, H Jiang, S Witchel, N Gurtunca, Svetlana A Yatsenko, D Mysliwec, K Topaloglu, Aleksandar Rajkovic
Novel inactivating mutations of the DCAF17 gene in American and Turkish families cause male infertility and female subfertility in the mouse model. Clinical genetics 93 (4) (2018)
Yu Ren, Feiyang Diao, Sunita Katari, Svetlana A Yatsenko, Huaiyang Jiang, Michelle A Wood-Trageser, Aleksandar Rajkovic
Functional study of a novel missense single-nucleotide variant of NUP107 in two daughters of Mexican origin with premature ovarian insufficiency. Molecular genetics & genomic medicine 6 (2) (2018)

Aleksandar Rajkovic.css-eqlu8i{font-size:small;padding-left:4px;} (A Rajkovic)

Publication Activity (10 Years)

Top Topics

Top Venues

Aleksandar Rajkovic (A Rajkovic)