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How to Create a Study Plan for the Genetic Counseling Board Exam | Featuring Brianna Tucker, MS, CGC
We are joined by Brianna Tucker, MS, CGC, a genetic counselor who graduated from Stanford's Genetic Counseling program in 2023. Brianna discusses her approach for creating a successful 6-month study plan for the ABGC board exam, which she took in March 2024.
Brianna used multiple strategies including flashcards with spaced repetition, flowcharts, and even songs to help learn the material. Brianna created a study planner and progress tracker using Google sheets, which she walks us through in the second half of the video. Brianna also discusses some of the challenges she faced in creating a study plan and how she held herself accountable while studying.
📍Time Stamps:
0:00 - Introduction and overview
3:05 - Day-to-day while studying
5:10 - Tools & techniques used to study
7:50 - Adapting study approach to different topics
8:50 - Creating flashcards & spaced repetition
10:30 - Incorporating practice questions
15:10 - Brianna's study planner
17:30 - Brianna's weekly structure
22:10 - Brianna's progress tracker
23:45 - Adjusting the study plan
📂 Links and resources mentioned:
Brianna’s Study Planner (feel free to make a copy for your own use) - docs.google.com/spreadsheets/d/1dLd9vP7mlx6WSiTxeahjkLse2JBvbsGcugfwjunRazE/edit
Resources for Studying (from Brianna)
1. Info about effective learning. Covers how to learn and tips for making flashcards (including examples). Brianna states that this resource "was very helpful for me in terms of figuring out how to learn so much content." www.supermemo.com/en/blog/twenty-rules-of-formulating-knowledge
2. Basic tips for making effective flashcards - blog.cambridgecoaching.com/how-to-make-baller-flashcards
3. General info about using spaced repetition for flashcard review - upchieve.org/blog/spaced-repetition
Additional resources
- Anki - apps.ankiweb.net/
- LucidChart - www.lucidchart.com/pages/usecase/education
- StudyRare ABGC Board Review Bootcamp - studyrare.com/registration
If you have questions or want to share your own study strategies, leave a comment below!
Stay connected! Support our rare disease education efforts by subscribing to the StudyRare newsletter for monthly board-style questions: studyrare.substack.com/
🔔 Don’t forget to like, subscribe, and hit the notification bell for more board prep tips!
You can also support our work by subscribing to this channel, following StudyRare on X/Twitter (@studyrare), or buying us a coffee: ko-fi.com/studyrare
Learn more about our work at www.studyrare.com
- Daniel
Переглядів: 26

Відео

Glycogen Storage Disease 1a (GSD1a) Song
Переглядів 1821 день тому
Lyrics "Look, I just pushed a script (script script) Ain’t no other patients that be doin’ this Glucose starts to drop, ayy, hit the floor Lactate and urate (uric acid) hit the top, ayy This a doll-face, baby, corn starch don’t ever stop It’s the flow that keeps the brain sharp, super, super sharp, ayy Give me Glycosade®, give me Glycosade I just drank what’s left like it’s Lemonade Lipids movi...
Master mucopolysaccharidosis types I-IX with this 2 minute song
Переглядів 47Місяць тому
Use this song to help you remember the key distinguishing features of each of the 7 types of mucopolysaccharidosis. Note that MPS V and MPS VIII are no longer used to designate a disease. Chapters: 0:00 Introduction 0:10 Molecular genetics 0:15 MPS I & II 0:45 MPS VII 0:56 MPS VI 1:05 MPS IV 1:15 MPS IX 1:26 MPS III 1:46 Treatment # Lyrics Mu-co-po-ly-saccharidosis to students much trouble it p...
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Переглядів 1842 місяці тому
In this video, we continue our discussion of imprinting disorders by focusing on Beckwith-Wiedemann syndrome (BWS) and Russell-Silver syndrome (RSS). These two conditions are associated with changes in the imprinted regions on chromosome 11p15. We delve into the genetic mechanisms underlying these disorders, including epigenetic alterations, copy number variations, and uniparental disomy (UPD)....
Imprinting disorders (Part 1): Prader-Willi and Angelman syndrome
Переглядів 2372 місяці тому
In this video, we provide an overview of the two most common imprinting disorders: Prader-Willi syndrome (PWS) and Angelman syndrome (AS). These disorders arise from changes in the imprinted region 15q11.2-q13, also known as the Prader-Willi / Angelman critical region. We explore the genetic mechanisms behind these disorders, including microdeletions (most commonly), uniparental disomy (UPD), a...
Risk calculations involving consanguinity (for the ABGC exam)
Переглядів 1042 місяці тому
In today's video, we calculate the risk for a couple (who are 1st cousins) of having a child with Joubert syndrome, an autosomal recessive disorder. This approach can be generally used for calculating the risk for recessive disorders in any pedigree where consanguinity is present. We also contrast this approach with the approach to risk calculations when there is no consanguinity present. The 2...
Relatedness, Consanguinity, and Coefficient of Inbreeding (for the ABGC exam)
Переглядів 1032 місяці тому
In this video, we cover the fundamentals of relatedness (both degree and coefficient of relatedness), consanguinity, and the coefficient of inbreeding. Note that at 10:20 and 11:48, I said "loci" though the correct term to use in this case is "allele." Definitions and Key Concepts: - Consanguinity: Occurs when a couple are blood relatives. Increases the risk for autosomal recessive disorders. -...
An Interview with Sonia Nessari, MS, GC (StudyRare Board Exam Scholarship Recipient)
Переглядів 633 місяці тому
This discussion features the 2024 StudyRare Board Exam Scholarship recipient, Sonia Nessari. Sonia is a prenatal genetic counselor at CooperSurgical, where she supports patients who are undergoing fertility treatments. While enrolled in graduate school, Sonia worked part-time as a Reproductive Clinical Operations Associate at Invitae to financially support her family as a single mother. Sonia c...
Congenital Heart Disease (Overview)
Переглядів 993 місяці тому
In this video, we provide an overview of congenital heart disease (CHD), which affects about 1% of all newborns in the United States. We explore several environmental (e.g. pregestational diabetes) and genetic (e.g. DiGeorge syndrome) factors associated with CHD. We also discuss 2 frameworks for sub-classifying congenital heart disease (cyanotic vs acyanotic, and syndromic vs non-syndromic). Ma...
Genetic Counselors Speak About Retaking the ABGC Board Exam (July 2024)
Переглядів 2303 місяці тому
This panel discussion features three genetic counselors (Caitlin, Bri, and Marisa) who successfully passed the ABGC exam in March 2024 after not passing on their first attempt. Through this discussion, the panelists share parts of their exam preparation journey as well as advice on how to prepare for a repeat attempt on the ABGC exam. In doing so, they help destigmatize the notion of needing to...
Multiple Choice Question Analysis: How to Learn from Practice Questions (for the ABGC Exam)
Переглядів 1534 місяці тому
The purpose of this video is to introduce the concept of "Question Analysis" (QA), a process that involves systematically reflecting and analyzing performance on multiple choice practice questions in preparation for board exams. The template discussed in this video was initially designed to help students analyze their performance on multiple choice questions during each review session of the AB...
Periodic paralysis syndromes
Переглядів 3026 місяців тому
In this video, I discuss the primary periodic paralysis syndromes, whose clinical hallmark is sudden-onset, short-term episodes of muscle weakness or paralysis. The PPP are due to variants in potassium, sodium, or calcium channels. In addition, the PPP can be classified as hypokalemic, normokalemic, or hyperkalemic, with these classifications being based on the observed serum potassium levels d...
Screening newborns for hearing loss
Переглядів 707 місяців тому
Screening newborns for hearing loss
Pompe disease
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Tips for preparing for the new ABGC exam (Jan 2024)
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Cystic Fibrosis
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Galactosemia
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Approach to Bayesian Calculations for ABGC and ABMGG Exams
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Diagnostic Approach to Ptosis
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Leber Congenital Amaurosis
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Alternating Hemiplegia of Childhood
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Disorders of Copper Transport (Wilson and Menkes disease)
Переглядів 191Рік тому
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Disorders of Polyamine Synthesis (Snyder-Robinson & Ornithine decarboxylase superactivity)
Переглядів 171Рік тому
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Question 56-57 | StudyRare Newsletter | A child with hyperpigmented streaks and developmental delays
Переглядів 99Рік тому
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Recombinant 8 Syndrome (aka San Luis Valley Syndrome)
Переглядів 166Рік тому
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Increased Nuchal Translucency
Переглядів 7 тис.2 роки тому
Increased Nuchal Translucency
Eyelid Terminology for the Geneticist
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Tyrosine Metabolism - A Clever Mnemonic!
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КОМЕНТАРІ

  • @CaptainHook4444
    @CaptainHook4444 18 днів тому

    I really liked this thank you

    • @studyrare
      @studyrare 18 днів тому

      Thank you very much for your kind comment and for watching!

  • @The_Kevinist
    @The_Kevinist 18 днів тому

    This is fucking trash.

  • @kadimetsamagi6417
    @kadimetsamagi6417 Місяць тому

    Mine is 1.6 . They say it is low

  • @briechz99-999
    @briechz99-999 2 місяці тому

    Super helpful video! Great job explaining this complex topic

    • @studyrare
      @studyrare 2 місяці тому

      Thank you, Bri! Will pass this along to Sofia.

  • @aman_ankush
    @aman_ankush 3 місяці тому

    Mind blowing video sir..thanku for such informative and easy animated video

    • @studyrare
      @studyrare 3 місяці тому

      thank you for watching and for your comment!

  • @makennamay2703
    @makennamay2703 3 місяці тому

    Very helpful! Thank you so much.

    • @studyrare
      @studyrare 3 місяці тому

      Thank you, Makenna! I am glad to hear that you found this video helpful!

  • @juliafield9381
    @juliafield9381 6 місяців тому

    Thank you so much for the video! I was just wondering if you could explain how the glutaryl coA forms gluatoconic acid and 3-OH-Glutaric acid?

  • @apputaaz6653
    @apputaaz6653 7 місяців тому

    Hi doctr i have 22 weeks pregnencyand my nuchal fold thickness is 6.6mm. Pls sugest me what i do.

    • @urushanepali3975
      @urushanepali3975 7 місяців тому

      I also have same problem I have 22 weeks 5days pregnancy my nuchal fold thickness is 7mm can u plz suggest me Doctor

    • @apputaaz6653
      @apputaaz6653 7 місяців тому

      ​@@urushanepali3975 am with for nipt test result .

  • @dilmiachinthika9891
    @dilmiachinthika9891 10 місяців тому

    Hi doctor my nuchal fold is 5mm 21 weeks and 5 days it is normal or problem

  • @luche5228
    @luche5228 11 місяців тому

    Thank you for this very informative video.

    • @studyrare
      @studyrare 11 місяців тому

      No problem. Thank you for watching!

  • @kabitamaharjan8641
    @kabitamaharjan8641 Рік тому

    Hi doctor I have 20w of pregnant, and my Nuchal fold thickness value is 5.6 does it normal? And doctor recommended to do Nipt test I’m waiting for the report.i’m in too tens...😢😢😢 plz doctor suggest me

    • @studyrare
      @studyrare Рік тому

      Hello, yes, the criteria for nuchal fold thickness changes with gestational age. At 20 weeks, the nuchal fold thickness is usually less than 6 mm. I would recommend following up with your OBGYN with any additional questions related to your pregnancy. Wishing you all the best! www.cuh.nhs.uk/patient-information/increased-nuchal-fold-nf/

    • @apputaaz6653
      @apputaaz6653 7 місяців тому

      Pls reply me how ur baby.my baby nf is 6.6mm.

  • @Metabolismo101
    @Metabolismo101 Рік тому

    Awesome!

  • @carlyle8969
    @carlyle8969 Рік тому

    Excellent video! Keep up the strong work!

    • @studyrare
      @studyrare Рік тому

      Thank you! I really appreciate it!

  • @duai7090
    @duai7090 Рік тому

    Thank you

    • @studyrare
      @studyrare Рік тому

      You're welcome. Thank you for watching!

  • @zcombs5797
    @zcombs5797 Рік тому

    Can you differentiate genetic vs Intoxication via metabolic labs alone or are genetic tests required to rule out intoxication

  • @razanalnajjar9112
    @razanalnajjar9112 Рік тому

    Thankyouuuu so much 😭🙌 you saved my life!

    • @studyrare
      @studyrare Рік тому

      No problem, thank you for watching!

  • @dylanallen2499
    @dylanallen2499 Рік тому

    Great video, however the gene that causes IVA is called IVD, not IVA.

    • @studyrare
      @studyrare Рік тому

      That is correct. Thank you for pointing this out.

  • @lifeofshihtzu1699
    @lifeofshihtzu1699 Рік тому

    5.1mm is it abnormal😢. Plz reply me (13 weeks,)

  • @yulylaguadoherrera7957
    @yulylaguadoherrera7957 Рік тому

    Would yo like share with me the bibliography o de source of the metabolic pathway of leucine

  • @hanumanthreddychilapalli7849

    Nuchal translucency measures 4.76 mm; it appears thickened. Also suspicious small cystic areas are noted under the skin behind the neck. Findings are highly suspicious for? cystic hygroma.

    • @hanumanthreddychilapalli7849
      @hanumanthreddychilapalli7849 Рік тому

      @medMuse is there any problem with above results please respond on it thank you

    • @studyrare
      @studyrare Рік тому

      Hello, I apologize for the delayed response. Cystic hygromas can sometimes happen on their own, though can also be associated with underlying genetic disorders like Down syndrome, Turner syndrome or Noonan syndrome. The findings of a cystic hygroma usually warrants closer follow-up by your local OBGYN.

  • @lamaabdulrhman7975
    @lamaabdulrhman7975 Рік тому

    12 week CRL 52.4 and NT 1.5 ,, is it normal ?

  • @BradleyH
    @BradleyH Рік тому

    Thank you for this video. Your slide at 2-3 mins says Biotin (vitamin B2) as a cofactor of glutaryl CoA. Can you clarify? Is it both biotin + B2? Or is there a possible mistake of calling B2 as biotin, or riboflavin as B7?

    • @studyrare
      @studyrare Рік тому

      Thank you for your comment. Yes, you are correct, this should read as "Riboflavin (vitamin B2)". Biotin is not a cofactor for glutaryl-CoA dehydrogenase. The acyl-CoA dehydrogenases (including glutaryl-CoA dehydrogenase) all use FAD (flavin adenine dinucleotide) as a cofactor. Ribo'flavin' is a precursor to FAD and is therefore a cofactor for this family of enzymes.

  • @sweetrainydays
    @sweetrainydays Рік тому

    Is the NT value the lower the better? I am 13w and my Nt was 2.4mm, Crl 67mm. Is 2mm considered safer than 2.4mm? Or as long as Nt value is <95% it doesn’t matter? Thank you

    • @studyrare
      @studyrare Рік тому

      Thank you for your question. In general, as long as NT value is <95%, then you are within the range of normal NT values in for 95% of healthy pregnancies. We would say that you are not at any increased risk for fetal anomalies with an NT below 95%. There is some variability in NT values within healthy pregnancies, and lower is not necessarily "better". As an example, your pregnancy would not be at an increased risk being at the 90th percentile compared with the 50th percentile, assuming no other anomalies were found.

    • @mlopresti6197
      @mlopresti6197 Рік тому

      @@studyrarewhere are you getting the percentiles from? I had my NT scan recently and it was 2.3mm with a CRL of 72.2mm. I found some calculators online and one of them said it was above 95th percentile while the others said it was around 80th. Which one is right? I’ve been worried sick.

    • @aarthikrishna3967
      @aarthikrishna3967 Рік тому

      Sister how is ur baby now ..me too have the same nt value

    • @sweetrainydays
      @sweetrainydays Рік тому

      @@aarthikrishna3967 he is a healthy 3.5month old!

  • @AnnettaMazzeo
    @AnnettaMazzeo Рік тому

    Hello Doctor, I’ve done an early ultrasound I’m 10+1 weeks and they found A 3,4mm Nt!! Don I have to be worried? Thanks

    • @studyrare
      @studyrare Рік тому

      Hello Anna, thank you for your message. It is hard for me to say based on the NT value alone. If this was the only finding, then based on the chart in minute 3, the most likely outcome would still be a healthy pregnancy. Your OBGYN would be best equipped to answer this question and can combine the ultrasound fundings and any other studies to help put the NT value into context and discuss next steps.

  • @nasrinkhatun3389
    @nasrinkhatun3389 2 роки тому

    Hello med use, My baby nuchal fold thickness 2.6 mm And my pregnancy is 21 weeks. Is it normal? And what should I do now? Plz suggest me

    • @studyrare
      @studyrare 2 роки тому

      Hello Nasrin, thank you for your message. The nuchal fold thickness 2.6 mm at your gestational age would generally not qualify as thick. However, I unfortunately cannot give medical advice over the internet, this is something that can be best discussed with your local OBGYN.

    • @juliekaye363
      @juliekaye363 Рік тому

      Watch the video

  • @nicolasdastous6360
    @nicolasdastous6360 2 роки тому

    hey @medMuse , very nice video. My wife is pregnant, we wen't for our dating echo last week at 11 weeks. The NT was 5.7mm. we were devastated. We went back at 12 weeks, the NT was 2.3mm. the doctor said she never saw that. We went from high risk to normal in one week. We also did the DNA blood work, all came back negative.

    • @studyrare
      @studyrare 2 роки тому

      Hi Nicolas, thanks for your comment and for sharing your experience. So glad to hear that baby's NT is back to normal. Wishing you and your wife a healthy and safe pregnancy.

    • @lamaabdulrhman7975
      @lamaabdulrhman7975 Рік тому

      How is your baby

    • @nicolasdastous6360
      @nicolasdastous6360 Рік тому

      @@studyrare Shes at 34 weeks!! can't wait :)

    • @Sharma-tr555ob
      @Sharma-tr555ob Рік тому

      How is your baby mam plz reply me sem problem me

    • @Sharma-tr555ob
      @Sharma-tr555ob Рік тому

      🙏plz batana mam aapki baby kase h mera bhi nt 4mm or one weeks me 2.9 aaya h nipt test likha h docter ne

  • @muhammadwaqas1091
    @muhammadwaqas1091 2 роки тому

    My son Burhan also involved in IVA. Pakistan

  • @212_subashg3
    @212_subashg3 3 роки тому

    This was helpful thx:)

    • @studyrare
      @studyrare 2 роки тому

      No problem! Glad you found it helpful!

  • @jesiraj2448
    @jesiraj2448 3 роки тому

    Thank you , great informative review. Please do make more medical genetics vedeos.

    • @studyrare
      @studyrare 2 роки тому

      Will do, thanks for your feedback!

  • @PediatricBoardwithDrAsala
    @PediatricBoardwithDrAsala 3 роки тому

    nice .. thanks

  • @susannerack8541
    @susannerack8541 3 роки тому

    Hey. I liked the video. I have been trying to search for a knowledgable UA-cam vid like yours that teaches everything in this UA-cam video.Your breakdown actually is like the videos from this informative health enthusiast Dr Ethan! Ethan's videos are helpful and I learned a lot for wellness. He is an educational health enthusiast in Europe and he explains mental health! You should check out his UA-cam out and give Dr Ethan a like! ➡️ #DoctorEthanNHS

  • @lisagonzalez2902
    @lisagonzalez2902 4 роки тому

    Thank you!

    • @studyrare
      @studyrare 2 роки тому

      You're welcome, Lisa!

  • @savindrachathu7653
    @savindrachathu7653 4 роки тому

    Really good presentation that covers everything about the topic. Please know that you are amazing!

    • @studyrare
      @studyrare 2 роки тому

      Thank you, I appreciate it!

    • @nukenelson
      @nukenelson 2 роки тому

      Awesome presentation..crisp and precise

  • @rubabmarham57
    @rubabmarham57 5 років тому

    My son is suffering PA. I need help

    • @javerialaghari2604
      @javerialaghari2604 4 роки тому

      How is ur son now.. My son was also diagnosed with this metabolic disorder n he could not survive

    • @studyrare
      @studyrare 2 роки тому

      I am sorry to hear this, Rubab. Javeria, I am also sorry to hear about your son.